hand, foot and mouth disease

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Results for "hand, foot and mouth disease": 1005 gene sets

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hand, foot and mouth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hand, foot and mouth disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease hand, foot and mouth disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Hand, Foot and Mouth Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hand, Foot and Mouth Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hand, Foot And Mouth Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hand, Foot And Mouth Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
hand, foot and mouth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
CV-A6-associated hand, foot, and mouth disease (severe vs mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the CV-A6-associated hand, foot, and mouth disease (severe vs mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Split-hand/foot malformation 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Split-hand/foot malformation 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Split-hand/foot malformation 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hand foot uterus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hand foot uterus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Split hand foot deformity 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split hand foot deformity 1 from the curated CTD Gene-Disease Associations dataset.
Split-Hand/Foot Malformation 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation 6 from the curated CTD Gene-Disease Associations dataset.
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset.
Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset.
Split-Hand/Foot Malformation 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation 4 from the curated CTD Gene-Disease Associations dataset.
Split-Hand/Foot Malformation 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation 5 from the curated CTD Gene-Disease Associations dataset.
SPLIT-HAND/FOOT MALFORMATION 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPLIT-HAND/FOOT MALFORMATION 2 from the curated CTD Gene-Disease Associations dataset.
Hand foot uterus syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hand foot uterus syndrome from the curated CTD Gene-Disease Associations dataset.
Split-hand/foot malformation with long bone deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset.
hand-foot-uterus syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hand-foot-uterus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
split hand/foot malformation 2 Gene Set From OMIM Gene-Disease Associations genes associated with the split hand/foot malformation 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
split hand/foot malformation 1 Gene Set From OMIM Gene-Disease Associations genes associated with the split hand/foot malformation 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation 3, gene duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 3, gene duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation with long bone deficiency 3 Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation with long bone deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation with long bone deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation 6 Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation 4 Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation 5 Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
Split-Hand/Foot Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand/Foot Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Split-Hand-Foot Malformation With Long Bone Deficiency 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Long Bone Deficiency 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Split-Hand-Foot Malformation With Sensorineural Hearing Loss Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hand Foot Uterus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hand Foot Uterus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
hand-foot-genital syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease hand-foot-genital syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
hand-foot-genital syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hand-foot-genital syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation 1 with sensorineural hearing loss Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 1 with sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Split hand-foot malformation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Split hand-foot malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hand-foot-genital syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand-foot-genital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
deviation of the hand or of fingers of the hand Gene Set From HPO Gene-Disease Associations genes associated with the deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
radial deviation of the hand or of fingers of the hand Gene Set From HPO Gene-Disease Associations genes associated with the radial deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ulnar deviation of the hand or of fingers of the hand Gene Set From HPO Gene-Disease Associations genes associated with the ulnar deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Deviation Of The Hand Or Of Fingers Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The Hand Or Of Fingers Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand osteoarthritis severity (hand Klsum) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hand osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; mouth neoplasms; papillomavirus infections; pharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; mouth neoplasms; papillomavirus infections; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease mouth disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
mouth disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease mouth disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
mouth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
genetic predisposition to disease; mouth neoplasms; neoplasms, squamous cell Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease; mouth neoplasms; neoplasms, squamous cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease mouth disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Mouth disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Mouth disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Mouth disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Mouth disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Mouth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Foot ulcer in diabetes and neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Foot ulcer in diabetes and neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
charcot-marie-tooth disease, foot deformity of Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, foot deformity of phenotype from the curated OMIM Gene-Disease Associations dataset.
Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Low hand grip strength (60 years and older) (EWGSOP) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low hand grip strength (60 years and older) (EWGSOP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Low hand grip strength (60 years and older) (FNIH) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low hand grip strength (60 years and older) (FNIH) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiminicore Disease, Moderate, With Hand Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiminicore Disease, Moderate, With Hand Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Crohn's disease and celiac disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Crohn's disease and celiac disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Primary somatosensory area, mouth, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, mouth, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, mouth, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, mouth Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, mouth, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, mouth, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, mouth, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Mouth Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mouth Diseases from the curated CTD Gene-Disease Associations dataset.
Mouth Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mouth Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mouth Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mouth Neoplasms from the curated CTD Gene-Disease Associations dataset.
burning mouth syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease burning mouth syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carcinoma, squamous cell; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; cocarcinogenesis; mouth neoplasms; papillomavirus infections; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cocarcinogenesis; mouth neoplasms; papillomavirus infections; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; papillomavirus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; neoplasm metastasis; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; neoplasm metastasis; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, squamous cell; lung neoplasms; mouth neoplasms; neoplasm of lung ; squamous cell carcinoma; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; lung neoplasms; mouth neoplasms; neoplasm of lung ; squamous cell carcinoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; precancerous conditions; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; precancerous conditions; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth, edentulous; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth, edentulous; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukoplakia; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease leukoplakia; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; papillomavirus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; mouth diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; mouth diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; maxillary neoplasms; mouth neoplasms; tongue neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; maxillary neoplasms; mouth neoplasms; tongue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; embolism; eosinophilia; mouth neoplasms; neoplasm invasiveness; neoplasm recurrence, local; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; embolism; eosinophilia; mouth neoplasms; neoplasm invasiveness; neoplasm recurrence, local; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; neovascularization, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; lymphatic metastasis; mouth neoplasms; oropharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; lymphatic metastasis; mouth neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cocarcinogenesis; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cocarcinogenesis; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; mouth neoplasms; squamous cell carcinoma; tongue neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; mouth neoplasms; squamous cell carcinoma; tongue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; leukoplakia; mouth neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia; mouth neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; fibrosis; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; fibrosis; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; carcinoma, squamous cell; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cervical neoplasm; mouth neoplasms; uterine cervical neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cervical neoplasm; mouth neoplasms; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms; respiratory tract neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; tongue neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; tongue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; cell transformation, neoplastic; genomic instability; leukoplakia, oral; mouth neoplasms; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cell transformation, neoplastic; genomic instability; leukoplakia, oral; mouth neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
esophageal neoplasms; flushing; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; flushing; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; lymphatic metastasis; mouth neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; lymphatic metastasis; mouth neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukoplakia, oral; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease leukoplakia, oral; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; mouth abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; mouth abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; leukoplakia, oral; lichen planus, oral; mouth neoplasms; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; lichen planus, oral; mouth neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; neoplasm recurrence, local Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal neoplasms; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal neoplasms; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; oropharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms; pharyngeal neoplasms; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; pharyngeal neoplasms; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; inflammation; mouth neoplasms; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; inflammation; mouth neoplasms; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; lymphatic metastasis; mouth neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; lymphatic metastasis; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mouth in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
epiboly involved in gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2015 genes participating in the epiboly involved in gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2015 dataset.
gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2015 genes participating in the gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2015 dataset.
mouth neoplasm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the mouth neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the mouth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
triangular mouth Gene Set From HPO Gene-Disease Associations genes associated with the triangular mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
wide mouth Gene Set From HPO Gene-Disease Associations genes associated with the wide mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular-shaped open mouth Gene Set From HPO Gene-Disease Associations genes associated with the triangular-shaped open mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
downturned corners of mouth Gene Set From HPO Gene-Disease Associations genes associated with the downturned corners of mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of mouth size Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of mouth size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
open mouth Gene Set From HPO Gene-Disease Associations genes associated with the open mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
narrow mouth Gene Set From HPO Gene-Disease Associations genes associated with the narrow mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of mouth shape Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of mouth shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the mouth Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mouth Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mouth Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mouth, Edentulous Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mouth, Edentulous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mouth Abnormalities Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mouth Abnormalities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mouth Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mouth Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Burning Mouth Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Burning Mouth Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal mouth morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mouth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mucosal lining of the mouth Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mucosal lining of the mouth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mouth mucosal ulcer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mouth mucosal ulcer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent mouth Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent mouth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased mouth tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased mouth tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mouth Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue mouth from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
mouth Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue mouth in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
mouth Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue mouth in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Erythroplakia Of Mouth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erythroplakia Of Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Burning Mouth Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Burning Mouth Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Squamous Cell Carcinoma Of Mouth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Squamous Cell Carcinoma Of Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Carcinoma In Situ Of Mouth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma In Situ Of Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Fibrous Hyperplasia Of Mouth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Fibrous Hyperplasia Of Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Mouth Ulcers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Mouth Ulcers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Downturned Corners Of Mouth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Downturned Corners Of Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Open Mouth (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Open Mouth (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Mouth Size Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Mouth Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Triangular Mouth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Triangular Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Asymmetry Of The Mouth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Asymmetry Of The Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Triangular-Shaped Open Mouth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Triangular-Shaped Open Mouth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2023 genes participating in the gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2023 dataset.
ingression involved in gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2023 genes participating in the ingression involved in gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2023 dataset.
epiboly involved in gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2023 genes participating in the epiboly involved in gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal mouth morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mouth morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mouth floor morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mouth floor morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
mouth mucosal ulcer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the mouth mucosal ulcer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent mouth Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent mouth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased mouth size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mouth size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
down-turned corners of mouth Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the down-turned corners of mouth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased mouth size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mouth size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mouth morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal mouth morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2025 genes participating in the gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2025 dataset.
ingression involved in gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2025 genes participating in the ingression involved in gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2025 dataset.
epiboly involved in gastrulation with mouth forming second Gene Set From GO Biological Process Annotations 2025 genes participating in the epiboly involved in gastrulation with mouth forming second biological process from the curated GO Biological Process Annotations 2025 dataset.
Burning mouth syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Burning mouth syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mouth Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Mouth from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Mouth Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Mouth in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Mouth Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Mouth in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Mouth floor Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Mouth floor in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Wide mouth Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Wide mouth phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mouth morphology (principal component model) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mouth morphology (principal component model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
coronary artery disease; coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; graves disease; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; disease susceptibility Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis; crohn disease; crohn's disease; disease models, animal Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; graft vs host disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
glial limiting end-foot Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the glial limiting end-foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
astrocyte end-foot Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the astrocyte end-foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
astrocyte end-foot Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the astrocyte end-foot cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
foot layer Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the foot layer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Foot Dermatoses Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Foot Dermatoses from the curated CTD Gene-Disease Associations dataset.
Foot Deformities, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Foot Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.
diabetic foot Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetic foot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes complications; diabetic angiopathies; diabetic foot; syndrome; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; diabetic angiopathies; diabetic foot; syndrome; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; diabetic foot; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; diabetic foot; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
foot Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term foot in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
glial limiting end-foot Gene Set From GO Cellular Component Annotations 2015 proteins localized to the glial limiting end-foot cellular component from the curated GO Cellular Component Annotations 2015 dataset.
astrocyte end-foot Gene Set From GO Cellular Component Annotations 2015 proteins localized to the astrocyte end-foot cellular component from the curated GO Cellular Component Annotations 2015 dataset.
sclerosis of foot bone Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sclerosis of foot bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
foot dorsiflexor weakness Gene Set From HPO Gene-Disease Associations genes associated with the foot dorsiflexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long foot Gene Set From HPO Gene-Disease Associations genes associated with the long foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
foot polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
narrow foot Gene Set From HPO Gene-Disease Associations genes associated with the narrow foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the plantar skin of foot Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the plantar skin of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the foot Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
positional foot deformity Gene Set From HPO Gene-Disease Associations genes associated with the positional foot deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
preaxial foot polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the preaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
split foot Gene Set From HPO Gene-Disease Associations genes associated with the split foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sclerosis of foot bone Gene Set From HPO Gene-Disease Associations genes associated with the sclerosis of foot bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rocker bottom foot Gene Set From HPO Gene-Disease Associations genes associated with the rocker bottom foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital foot contractures Gene Set From HPO Gene-Disease Associations genes associated with the congenital foot contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the foot musculature Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the foot musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short foot Gene Set From HPO Gene-Disease Associations genes associated with the short foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad foot Gene Set From HPO Gene-Disease Associations genes associated with the broad foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
medial deviation of the foot Gene Set From HPO Gene-Disease Associations genes associated with the medial deviation of the foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
valgus foot deformity Gene Set From HPO Gene-Disease Associations genes associated with the valgus foot deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal foot bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
postaxial polysyndactyly of foot Gene Set From HPO Gene-Disease Associations genes associated with the postaxial polysyndactyly of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
postaxial foot polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the postaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mesoaxial foot polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the mesoaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Foot Dermatoses Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Foot Dermatoses phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Foot Ulcer Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Foot Ulcer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Diabetic Foot Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Diabetic Foot phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Foot Deformities, Congenital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Foot Deformities, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal hind foot hair pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal foot pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal foot pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fused podocyte foot processes Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fused podocyte foot processes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent podocyte foot process Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent podocyte foot process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
podocyte foot process effacement Gene Set From MPO Gene-Phenotype Associations gene mutations causing the podocyte foot process effacement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dark foot pads Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dark foot pads phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal foot pad morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal foot pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal podocyte foot process morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal podocyte foot process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal foot plate morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal foot plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased foot pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased foot pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
synpolydactyly with foot anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the synpolydactyly with foot anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
foot Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue foot from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
foot sole Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue foot sole from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
foot muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue foot muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
foot sole Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue foot sole in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
foot Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue foot in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
tube foot Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tube foot in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Foot Osteomyelitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Foot Osteomyelitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Foot Deformity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Foot Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Split Foot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Split Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Foot Ulcer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Foot Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Flat Foot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Flat Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Flat Foot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Flat Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Positional Foot Deformity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Positional Foot Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Penetrating Foot Ulcers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Penetrating Foot Ulcers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postaxial Foot Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Postaxial Foot Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Foot Contraction Deformities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Foot Contraction Deformities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postaxial Polysyndactyly Of Foot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Postaxial Polysyndactyly Of Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Foot Bone Ossification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Foot Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mesoaxial Foot Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mesoaxial Foot Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Split-Foot Malformation With Mesoaxial Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Split-Foot Malformation With Mesoaxial Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Foot Drop Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Foot Drop in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Foot Drop Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Foot Drop in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Foot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Foot Contractures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Foot Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Foot Dorsiflexor Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Dorsiflexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Narrow Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gait, Drop Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gait, Drop Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Structural Foot Deformity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Structural Foot Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Long Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foot Oligodactyly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Oligodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cavovarus Deformity Of Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cavovarus Deformity Of Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Equinovarus Deformity Of Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Equinovarus Deformity Of Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Foot Musculature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Foot Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Medial Deviation Of The Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Medial Deviation Of The Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foot Acroosteolysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Preaxial Foot Polydactyly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Preaxial Foot Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Podocyte Foot Process Effacement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Podocyte Foot Process Effacement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Absence Of Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Absence Of Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foot Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cramp In Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cramp In Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
podocyte foot Gene Set From GO Cellular Component Annotations 2023 proteins localized to the podocyte foot cellular component from the curated GO Cellular Component Annotations 2023 dataset.
astrocyte end-foot Gene Set From GO Cellular Component Annotations 2023 proteins localized to the astrocyte end-foot cellular component from the curated GO Cellular Component Annotations 2023 dataset.
glial limiting end-foot Gene Set From GO Cellular Component Annotations 2023 proteins localized to the glial limiting end-foot cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal foot pad morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal foot pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal podocyte foot process morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal podocyte foot process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fused podocyte foot processes Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fused podocyte foot processes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
podocyte foot process effacement Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the podocyte foot process effacement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal foot pigmentation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal foot pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent podocyte foot process Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent podocyte foot process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased foot pigmentation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased foot pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased foot pad pigmentation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased foot pad pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hind foot hair pigmentation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
podocyte foot Gene Set From GO Cellular Component Annotations 2025 proteins localized to the podocyte foot cellular component from the curated GO Cellular Component Annotations 2025 dataset.
astrocyte end-foot Gene Set From GO Cellular Component Annotations 2025 proteins localized to the astrocyte end-foot cellular component from the curated GO Cellular Component Annotations 2025 dataset.
glial limiting end-foot Gene Set From GO Cellular Component Annotations 2025 proteins localized to the glial limiting end-foot cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Foot Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Foot from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Foot sole Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Foot sole from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Foot Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Foot in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Foot sole Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Foot sole in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Foot muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Foot muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Tube foot Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Tube foot in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Astrocyte end-foot Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Astrocyte end-foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Podocyte foot Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Podocyte foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Glial limiting end-foot Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Glial limiting end-foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Podocyte foot Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Podocyte foot cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Astrocyte end-foot Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Astrocyte end-foot cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Foot layer Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Foot layer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Glial limiting end-foot Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Glial limiting end-foot cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Postaxial foot polydactyly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Postaxial foot polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Foot dorsiflexor weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Foot dorsiflexor weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Split-foot malformation-mesoaxial polydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Split-foot malformation-mesoaxial polydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spondylometaepiphyseal dysplasia short limb-hand type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Heart-hand syndrome, Slovenian type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heart-hand syndrome, Slovenian type from the curated CTD Gene-Disease Associations dataset.
Craniofacial deafness hand syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniofacial deafness hand syndrome from the curated CTD Gene-Disease Associations dataset.
Hand Dermatoses Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hand Dermatoses from the curated CTD Gene-Disease Associations dataset.
Hand Deformities, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hand Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.
Hand Strength Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Hand Strength in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
hand dermatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hand dermatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dermatitis, contact; hand dermatoses Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, contact; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, atopic; eczema; eczema allergic; hand dermatoses Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, atopic; eczema; eczema allergic; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hand strength Gene Set From GAD Gene-Disease Associations genes associated with the disease hand strength in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, allergic contact; hand dermatoses Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, allergic contact; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart-hand syndrome, holt-oram syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, atopic; dermatitis, irritant; dermatitis, occupational; hand dermatoses Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, atopic; dermatitis, irritant; dermatitis, occupational; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hand Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hand in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Relative hand skill in reading disability Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
abnormality of the hand Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sclerosis of hand bone Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sclerosis of hand bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal ossification of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular sclerosis of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the irregular sclerosis of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bracket epiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the bracket epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteolytic defects of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypotrophy of the small hand muscles Gene Set From HPO Gene-Disease Associations genes associated with the hypotrophy of the small hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
patchy sclerosis of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the patchy sclerosis of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the middle phalanx of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand tremor Gene Set From HPO Gene-Disease Associations genes associated with the hand tremor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the broad phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
valgus hand deformity Gene Set From HPO Gene-Disease Associations genes associated with the valgus hand deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
radial deviation of the hand Gene Set From HPO Gene-Disease Associations genes associated with the radial deviation of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand clenching Gene Set From HPO Gene-Disease Associations genes associated with the hand clenching phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cold-induced hand cramps Gene Set From HPO Gene-Disease Associations genes associated with the cold-induced hand cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of hand joint mobility Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of hand joint mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bullet-shaped phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the bullet-shaped phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent hand Gene Set From HPO Gene-Disease Associations genes associated with the absent hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ulnar deviation of the hand Gene Set From HPO Gene-Disease Associations genes associated with the ulnar deviation of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular ossification of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the irregular ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thimble-shaped middle phalanges of hand Gene Set From HPO Gene-Disease Associations genes associated with the thimble-shaped middle phalanges of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the duplication of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism affecting the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism affecting the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ivory epiphyses of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the ivory epiphyses of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pseudoepiphyses of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the pseudoepiphyses of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bracket epiphyses of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the bracket epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness of the intrinsic hand muscles Gene Set From HPO Gene-Disease Associations genes associated with the weakness of the intrinsic hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hyperextensible hand joints Gene Set From HPO Gene-Disease Associations genes associated with the hyperextensible hand joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphyses of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteolytic defects of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint contracture of the hand Gene Set From HPO Gene-Disease Associations genes associated with the joint contracture of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-shaped epiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the cone-shaped epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
synostosis involving bones of the hand Gene Set From HPO Gene-Disease Associations genes associated with the synostosis involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mesoaxial hand polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the mesoaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism affecting the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal hand morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
poor hand-eye coordination Gene Set From HPO Gene-Disease Associations genes associated with the poor hand-eye coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the middle phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the middle phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small hand Gene Set From HPO Gene-Disease Associations genes associated with the small hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteolytic defects of the hand bones Gene Set From HPO Gene-Disease Associations genes associated with the osteolytic defects of the hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphyses of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-shaped epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the cone-shaped epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
trident hand Gene Set From HPO Gene-Disease Associations genes associated with the trident hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thin proximal phalanges with broad epiphyses of the hand Gene Set From HPO Gene-Disease Associations genes associated with the thin proximal phalanges with broad epiphyses of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-shaped epiphyses of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the cone-shaped epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sclerosis of hand bone Gene Set From HPO Gene-Disease Associations genes associated with the sclerosis of hand bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal hand bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
preaxial hand polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the preaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bullet-shaped middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the bullet-shaped middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of phalangeal joints of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of phalangeal joints of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
radial club hand Gene Set From HPO Gene-Disease Associations genes associated with the radial club hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short tubular bones (hand) Gene Set From HPO Gene-Disease Associations genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pseudoepiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
split hand Gene Set From HPO Gene-Disease Associations genes associated with the split hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ivory epiphyses of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the ivory epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
postaxial hand polydactyly Gene Set From HPO Gene-Disease Associations genes associated with the postaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pseudoepiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the musculature of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the hand muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hand Deformities, Congenital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hand Deformities, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
IQ motif, EF-hand binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the IQ motif, EF-hand binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-hand domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-hand domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-hand, Ca insensitive Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-hand, Ca insensitive protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ISWI, HAND domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ISWI, HAND domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF hand associated, type-2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF hand associated, type-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF hand associated, type-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF hand associated, type-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-hand domain pair Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-hand domain pair protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-Hand 1, calcium-binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-Hand 1, calcium-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Phospholipase C, phosphoinositol-specific, EF-hand-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase C, phosphoinositol-specific, EF-hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adaptor protein Cbl, EF hand-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adaptor protein Cbl, EF hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-hand calcium-binding domain-containing protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-hand calcium-binding domain-containing protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-hand domain, type 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-hand domain, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF-hand domain, type 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF-hand domain, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
spondylometaepiphyseal dysplasia, short limb-hand type Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.
heart-hand syndrome, slovenian type Gene Set From OMIM Gene-Disease Associations genes associated with the heart-hand syndrome, slovenian type phenotype from the curated OMIM Gene-Disease Associations dataset.
craniofacial-deafness-hand syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the craniofacial-deafness-hand syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hand Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hand in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Hand Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hand Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Broad Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Broad Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spade-Like Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spade-Like Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Hand Flapping Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hand Flapping in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Claw Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Claw Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hand Eczema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hand Eczema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mesoaxial Hand Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mesoaxial Hand Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hand Monodactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hand Monodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symphalangism Affecting The Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symphalangism Affecting The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Hand Eczema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hand Eczema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infected Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infected Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stereotypical Hand Wringing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stereotypical Hand Wringing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Small Epiphyses Of The Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Epiphyses Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tenosynovitis Of Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tenosynovitis Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thimble-Shaped Middle Phalanges Of Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thimble-Shaped Middle Phalanges Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Hand Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Hand Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Radial Club Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Radial Club Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thin Proximal Phalanges With Broad Epiphyses Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thin Proximal Phalanges With Broad Epiphyses Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypotrophy Of The Small Hand Muscles Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypotrophy Of The Small Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heart-Hand Syndrome, Slovenian Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart-Hand Syndrome, Slovenian Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Curved Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Curved Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bullet-Shaped Middle Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bullet-Shaped Middle Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Craniofacial Deafness Hand Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Craniofacial Deafness Hand Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ivory Epiphyses Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ivory Epiphyses Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Large Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Of The Intrinsic Hand Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of The Intrinsic Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Clenching Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Clenching in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Osteolytic Defects Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteolytic Defects Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Radial Deviation Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radial Deviation Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Proximal Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Proximal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cold-Induced Hand Cramps Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cold-Induced Hand Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intrinsic Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrinsic Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Tubular Bones Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Tubular Bones Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hyperextensible Hand Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperextensible Hand Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of The Distal Phalanx Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of The Distal Phalanx Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ivory Epiphyses Of The Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ivory Epiphyses Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Trident Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Trident Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Hand Bone Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Hand Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Valgus Hand Deformity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Valgus Hand Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bullet-Shaped Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bullet-Shaped Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand-Wringing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand-Wringing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Irregular Ossification Of Hand Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregular Ossification Of Hand Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Poor Hand-Eye Coordination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Hand-Eye Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Hand Joint Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Hand Joint Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal hand joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hand joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
craniofacial-deafness-hand syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease craniofacial-deafness-hand syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Focal hand dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal hand dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
craniofacial-deafness-hand syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease craniofacial-deafness-hand syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondylometaepiphyseal dysplasia, short limb-hand type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondylometaepiphyseal dysplasia, short limb-hand type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hand dermatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hand dermatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hand Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hand in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Hand muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Heart-hand syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Heart-hand syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Craniofacial-deafness-hand syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Craniofacial-deafness-hand syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hand oligodactyly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand oligodactyly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aplasia/Hypoplasia of the phalanges of the hand Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia of the phalanges of the hand phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperextensible hand joints Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperextensible hand joints phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis-like hand anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis-like hand anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hand grip strength (Mahalanobis distance) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hand grip strength (Mahalanobis distance) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis of the hand Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis of the hand phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis (hand, severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis (hand, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hand grip strength Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hand grip strength phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Digit length ratio (right hand) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Digit length ratio (right hand) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Digit length ratio (left hand) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Digit length ratio (left hand) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Relative hand skill in reading disability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Relative hand skill Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relative hand skill phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Finger osteoarthritis severity (hand Klsum) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Finger osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thumb osteoarthritis severity (hand Klsum) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thumb osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
eye and adnexa disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye and adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
eye and adnexa disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye and adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
extrapyramidal and movement disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrapyramidal and movement disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autoimmune disease of skin and connective tissue Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eye and adnexa disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye and adnexa disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
proteinuria and cardiovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease proteinuria and cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acid lipase deficiency and cholesterol ester storage disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acid lipase deficiency and cholesterol ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease and ibd Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease and ibd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease and antioxidant enzyme defense Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease and antioxidant enzyme defense in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia and cardiovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia and cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease and myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease and myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolic syndrome and electrocardiographic coronary artery disease Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolic syndrome and electrocardiographic coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
liver disease, chronic and cirrhosis Gene Set From GAD Gene-Disease Associations genes associated with the disease liver disease, chronic and cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disease models, animal; neoplasms, germ cell and embryonal; testicular neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease disease models, animal; neoplasms, germ cell and embryonal; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease and vascular dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease and vascular dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease. plasma lipoproteins. and longevity Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease. plasma lipoproteins. and longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic stiffness and disease severity Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic stiffness and disease severity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease and plasma soluble thrombomodulin Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease and plasma soluble thrombomodulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ulcerative colitis and crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ulcerative colitis and crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary heart disease and plasma lipid levels. Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary heart disease and plasma lipid levels. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hpv infection and cervical disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hpv infection and cervical disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstructive pulmonary disease and disseminated bronchiectasis Gene Set From GAD Gene-Disease Associations genes associated with the disease obstructive pulmonary disease and disseminated bronchiectasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease and sarcoidosis (combined) Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease and sarcoidosis (combined) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occlusive artery disease and deep vein thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease occlusive artery disease and deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute neonatal disease and hyperammonemia Gene Set From GAD Gene-Disease Associations genes associated with the disease acute neonatal disease and hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary heart disease and serum very low density lipopro Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary heart disease and serum very low density lipopro in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cigarette smoking. coronary artery disease. and diabetes Gene Set From GAD Gene-Disease Associations genes associated with the disease cigarette smoking. coronary artery disease. and diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal function and chronic kidney disease Gene Set From GAD Gene-Disease Associations genes associated with the disease renal function and chronic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease and ulcerative colitis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease and ulcerative colitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Parkinson's disease (motor and cognition) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (motor and cognition) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Crohn's disease and psoriasis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Crohn's disease and psoriasis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Celiac disease and Rheumatoid arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Celiac disease and Rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chronic kidney disease and serum creatinine levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic kidney disease and serum creatinine levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal function and chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal function and chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
eye and adnexa disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease eye and adnexa disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
von willebrand disease, types 2a, 2b, 2m, and 2n Gene Set From OMIM Gene-Disease Associations genes associated with the von willebrand disease, types 2a, 2b, 2m, and 2n phenotype from the curated OMIM Gene-Disease Associations dataset.
lymphedema-distichiasis syndrome with renal disease and diabetes mellitus Gene Set From OMIM Gene-Disease Associations genes associated with the lymphedema-distichiasis syndrome with renal disease and diabetes mellitus phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From OMIM Gene-Disease Associations genes associated with the glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
polycystic kidney and hepatic disease Gene Set From OMIM Gene-Disease Associations genes associated with the polycystic kidney and hepatic disease phenotype from the curated OMIM Gene-Disease Associations dataset.
interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease, type 3, with spastic paraparesis and unusual plaques Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease, type 3, with spastic paraparesis and unusual plaques phenotype from the curated OMIM Gene-Disease Associations dataset.
sandhoff disease, infantile, juvenile, and adult forms Gene Set From OMIM Gene-Disease Associations genes associated with the sandhoff disease, infantile, juvenile, and adult forms phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease, type 3, with spastic paraparesis and apraxia Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease, type 3, with spastic paraparesis and apraxia phenotype from the curated OMIM Gene-Disease Associations dataset.
The role of Nef in HIV-1 replication and disease pathogenesis Gene Set From Reactome Pathways 2014 proteins participating in the The role of Nef in HIV-1 replication and disease pathogenesis pathway from the Reactome Pathways dataset.
Inflammatory Dry Skin And Bowel Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Dry Skin And Bowel Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Inflammatory Skin And Bowel Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Inflammatory Skin And Bowel Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycystic Kidney Disease, Potter Type I, With Microbrachycephaly, Hypertelorism, And Brachymelia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycystic Kidney Disease, Potter Type I, With Microbrachycephaly, Hypertelorism, And Brachymelia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Platelet Abnormalities With Eosinophilia And Immune-Mediated Inflammatory Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Platelet Abnormalities With Eosinophilia And Immune-Mediated Inflammatory Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Interstitial Lung, Joint, And Kidney Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Interstitial Lung, Joint, And Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Veno-Occlusive Disease And/Or Pulmonary Capillary Hemangiomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Veno-Occlusive Disease And/Or Pulmonary Capillary Hemangiomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Still'S Disease With Juvenile Onset And/Or Adult Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Still'S Disease With Juvenile Onset And/Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interstitial Lung And Liver Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interstitial Lung And Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lymphedema-Distichiasis Syndrome With Renal Disease And Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lymphedema-Distichiasis Syndrome With Renal Disease And Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interstitial Lung Disease, Nephrotic Syndrome, And Epidermolysis Bullosa, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interstitial Lung Disease, Nephrotic Syndrome, And Epidermolysis Bullosa, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia; Mixed Dementia; Frontotemporal Dementia Such As Pick'S Disease; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia; Mixed Dementia; Frontotemporal Dementia Such As Pick'S Disease; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glomerulocystic Kidney Disease With Hyperuricemia And Isosthenuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glomerulocystic Kidney Disease With Hyperuricemia And Isosthenuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alzheimer 39 s disease and miRNA effects Gene Set From WikiPathways Pathways 2024 proteins participating in the Alzheimer 39 s disease and miRNA effects pathway from the WikiPathways Pathways 2024 dataset.
ATM signaling in development and disease Gene Set From WikiPathways Pathways 2024 proteins participating in the ATM signaling in development and disease pathway from the WikiPathways Pathways 2024 dataset.
STING pathway in Kawasaki like disease and COVID 19 Gene Set From WikiPathways Pathways 2024 proteins participating in the STING pathway in Kawasaki like disease and COVID 19 pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC17A5 causes Salla disease (SD) and ISSD Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC17A5 causes Salla disease (SD) and ISSD pathway from the Reactome Pathways 2024 dataset.
The role of Nef in HIV-1 replication and disease pathogenesis Gene Set From Reactome Pathways 2024 proteins participating in the The role of Nef in HIV-1 replication and disease pathogenesis pathway from the Reactome Pathways 2024 dataset.
Autoimmune disease of skin and connective tissue Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autoimmune disease of skin and connective tissue from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autoimmune disease of skin and connective tissue Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autoimmune disease of skin and connective tissue in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction and alcohol associated liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune interstitial lung, joint, and kidney disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune interstitial lung, joint, and kidney disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune disease of skin and connective tissue Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune disease of eyes, ear, nose and throat Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of eyes, ear, nose and throat in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrapyramidal and movement disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrapyramidal and movement disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sickle cell disease and related diseases Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sickle cell disease and related diseases phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inflammatory skin and bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inflammatory skin and bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to muscle and heart glycogen synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle and heart glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal inflammatory skin and bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal inflammatory skin and bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuromuscular disease and ocular or auditory anomalies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuromuscular disease and ocular or auditory anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Estimated glomerular filtration rate in coronary artery disease and impaired kidney function Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Estimated glomerular filtration rate in coronary artery disease and impaired kidney function phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic disease (asthma, hay fever and/or eczema) (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Posterior cortical atrophy and Alzheimer's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior cortical atrophy and Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer disease and age of onset Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer disease and age of onset phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Celiac disease and Rheumatoid arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Celiac disease and Rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic bronchitis and chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic bronchitis and chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Dementia and core Alzheimer's disease neuropathologic changes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dementia and core Alzheimer's disease neuropathologic changes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Proteinuria and chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proteinuria and chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Deep ovarian and/or rectovaginal disease with dense adhesions Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Deep ovarian and/or rectovaginal disease with dense adhesions phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Kidney disease (early and late stages) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (early and late stages) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer's disease (onset between ages 58 and 79) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease (onset between ages 58 and 79) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body fat percentage and coronary artery disease (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and coronary artery disease (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and coronary artery disease (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and coronary artery disease (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index and coronary artery disease (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and coronary artery disease (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fever and diarrhea in mesalamine-treated irritable bowel disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fever and diarrhea in mesalamine-treated irritable bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Renal function and chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Renal function and chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pulmonary artery enlargement and chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary artery enlargement and chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson disease and lewy body pathology Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson disease and lewy body pathology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mood disorder and prion disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mood disorder and prion disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Behavioral disturbance or psychiatric symptoms and prion disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Behavioral disturbance or psychiatric symptoms and prion disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary artery disease and LDL cholesterol levels (multivariate analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease and LDL cholesterol levels (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary artery disease and triglyceride levels (multivariate analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease and triglyceride levels (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease and serum creatinine levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease and serum creatinine levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Psychosis and Alzheimer's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Psychosis and Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Crohn's disease and psoriasis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Crohn's disease and psoriasis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease (motor and cognition) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease (motor and cognition) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer’s disease and/or vascular dementia (clinical subgroup VaD+) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer’s disease and/or vascular dementia (clinical subgroup VaD+) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer’s disease and/or vascular dementia (clinical subgroup VaD++) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer’s disease and/or vascular dementia (clinical subgroup VaD++) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thyrotoxic hypokalemic periodic paralysis and Graves disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thyrotoxic hypokalemic periodic paralysis and Graves disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Medication use (drugs for peptic ulcer and gastro-oesophageal reflux disease) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Medication use (drugs for peptic ulcer and gastro-oesophageal reflux disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Type 2 diabetes and end-stage kidney disease in APOL1 risk genotype negative individuals Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 2 diabetes and end-stage kidney disease in APOL1 risk genotype negative individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital heart disease (anomalies of thoracic arteries and veins) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Congenital heart disease (anomalies of thoracic arteries and veins) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to antioxidants and zinc in age-related macular degeneration (disease progression) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antioxidants and zinc in age-related macular degeneration (disease progression) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
crohn disease; crohn's disease; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; peripheral arterial disease Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; granuloma Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
liver disease; wilson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; dna damage; genomic instability Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hemochromatosis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease ; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; cerebrovascular disease, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; sarcoidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison's disease; graves' disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney disease; vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; autoimmune diseases; graves disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; colitis, ulcerative; crohn disease Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult-onset still disease; still's disease, adult-onset Gene Set From GAD Gene-Disease Associations genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amnesia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; cerebrovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gaucher disease; nervous system diseases; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; metabolic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; coronary restenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft-versus-host disease; psoriasis; celiac disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease parkinson's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; peripheral vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; spondylitis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; gastrointestinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gaucher disease; legg-perthes disease; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease; ulcerative colitis; inflammatory bowel disease Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; postoperative complications; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; periodontal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; heart failure; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; dyslipidemias Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; osteoporosis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; disease susceptibility Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; disease susceptibility; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypertriglyceridemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; addison's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; hemochromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; ileal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsons disease; alzheimers disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; coronary artery disease; hyperlipidemias Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cadaver; coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene Set From GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
common variable immunodeficiency; crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; arteriosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; intestinal obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; dilatation, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lewy body disease; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyloidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperlipidemias Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sanhoff disease; tay-sachs disease Gene Set From GAD Gene-Disease Associations genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; postoperative complications; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hemochromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; delirium; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease/coronary artery disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; hallucinations Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; addison's disease; autoimmune diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroid disease; thyroid disease, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; genetic predisposition to disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; neural tube defects Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; spondylarthropathies Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylarthropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Cardiovascular Disease+Pulmonary Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiovascular Disease+Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease or first degree relation to individual with Parkinson's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease or first degree relation to individual with Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer's disease or family history of Alzheimer's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease or family history of Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

hand, foot and mouth disease Gene Set

hand, foot and mouth disease Gene Set

Hand, Foot and Mouth Disease Gene Set

Hand, Foot And Mouth Disease Gene Set

hand, foot and mouth disease Gene Set

CV-A6-associated hand, foot, and mouth disease (severe vs mild) Gene Set

Split-hand/foot malformation 6 Gene Set

Split-hand/foot malformation 4 Gene Set

Split-hand/foot malformation 1 Gene Set

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

Hand foot uterus syndrome Gene Set

Split hand foot deformity 1 Gene Set

Split-Hand/Foot Malformation 6 Gene Set

Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set

Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set

Split-Hand/Foot Malformation 4 Gene Set

Split-Hand/Foot Malformation 5 Gene Set

SPLIT-HAND/FOOT MALFORMATION 2 Gene Set

Hand foot uterus syndrome Gene Set

Split-hand/foot malformation with long bone deficiency Gene Set

hand-foot-uterus syndrome Gene Set

split hand/foot malformation 2 Gene Set

split hand/foot malformation 1 Gene Set

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

split-hand/foot malformation 3, gene duplication syndrome Gene Set

split-hand/foot malformation with long bone deficiency 3 Gene Set

split-hand/foot malformation with long bone deficiency 2 Gene Set

split-hand/foot malformation with long bone deficiency 1 Gene Set

split-hand/foot malformation 6 Gene Set

split-hand/foot malformation 4 Gene Set

split-hand/foot malformation 5 Gene Set

Split-Hand/Foot Malformation Gene Set

Split-Hand-Foot Malformation With Long Bone Deficiency 1 Gene Set

Split-Hand-Foot Malformation With Sensorineural Hearing Loss Gene Set

Hand Foot Uterus Syndrome Gene Set

hand-foot-genital syndrome Gene Set

hand-foot-genital syndrome Gene Set

Split hand-foot malformation 4 Gene Set

Split hand-foot malformation Gene Set

Split hand-foot malformation 1 with sensorineural hearing loss Gene Set

Split hand-foot malformation 1 Gene Set

Split hand-foot malformation 5 Gene Set

Split hand-foot malformation 2 Gene Set

Split hand-foot malformation 6 Gene Set

Split hand-foot malformation Gene Set

Hand-foot-genital syndrome Gene Set

deviation of the hand or of fingers of the hand Gene Set

radial deviation of the hand or of fingers of the hand Gene Set

ulnar deviation of the hand or of fingers of the hand Gene Set

Deviation Of The Hand Or Of Fingers Of The Hand Gene Set

Hand osteoarthritis severity (hand Klsum) Gene Set

addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set

Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set

carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma Gene Set

esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms Gene Set

esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene Set

carcinoma, squamous cell; head and neck neoplasms; mouth neoplasms; papillomavirus infections; pharyngeal neoplasms Gene Set

mouth disease Gene Set

mouth disease Gene Set

mouth disease Gene Set

genetic predisposition to disease; mouth neoplasms; neoplasms, squamous cell Gene Set

mouth disease Gene Set

Mouth disease Gene Set

Mouth disease Gene Set

Mouth disease Gene Set

Foot ulcer in diabetes and neuropathy Gene Set

charcot-marie-tooth disease, foot deformity of Gene Set

Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A Gene Set

Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Gene Set

Low hand grip strength (60 years and older) (EWGSOP) Gene Set

Low hand grip strength (60 years and older) (FNIH) Gene Set

Multiminicore Disease, Moderate, With Hand Involvement Gene Set

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set

Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

Crohn's disease and celiac disease Gene Set

Crohn's disease and celiac disease Gene Set

Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene Set