Congenital Fibrosis Of The Extraocular Muscles

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Results for "Congenital Fibrosis Of The Extraocular Muscles": 1004 gene sets

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congenital fibrosis of the extraocular muscles Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of the extraocular muscles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Congenital Fibrosis Of The Extraocular Muscles Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Fibrosis Of The Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital fibrosis of the extraocular muscles Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital fibrosis of the extraocular muscles from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital fibrosis of the extraocular muscles Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.
Fibrosis of extraocular muscles, congenital, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of Extraocular Muscles, Congenital, 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset.
Fibrosis Of Extraocular Muscles, Congenital, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset.
congenital fibrosis of extraocular muscles type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of extraocular muscles type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital fibrosis of extraocular muscles Gene Set From HPO Gene-Disease Associations genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fibrosis of extraocular muscles, congenital, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
fibrosis of extraocular muscles, congenital, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
fibrosis of extraocular muscles, congenital, 3b Gene Set From OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
fibrosis of extraocular muscles, congenital, 3a Gene Set From OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital fibrosis of the extraocular muscles 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital fibrosis of the extraocular muscles 3A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital fibrosis of extraocular muscles Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fibrosis Of Extraocular Muscles Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Extraocular Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
abnormality of the extraocular muscles Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Abnormality Of The Extraocular Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weak Extraocular Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weak Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
absent extraocular muscles Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent extraocular muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fibrosis; pulmonary fibrosis; scleroderma, systemic Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; pulmonary fibrosis; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital hepatic fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hepatic Fibrosis, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Fibrosis, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
myopathy of extraocular muscle Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy of extraocular muscle from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy of extraocular muscle Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extraocular retinoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extraocular retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extraocular Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term extraocular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
extraocular skeletal muscle development Gene Set From GO Biological Process Annotations 2015 genes participating in the extraocular skeletal muscle development biological process from the curated GO Biological Process Annotations 2015 dataset.
limited extraocular movements Gene Set From HPO Gene-Disease Associations genes associated with the limited extraocular movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal extraocular muscle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal extraocular muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
extraocular muscle Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue extraocular muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
extraocular muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue extraocular muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Extraocular Retinoblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extraocular Retinoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extraocular Muscle Paresis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extraocular Muscle Paresis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limited Extraocular Movements Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Extraocular Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Inferior Oblique Extraocular Muscle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Inferior Oblique Extraocular Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
extraocular skeletal muscle development Gene Set From GO Biological Process Annotations 2023 genes participating in the extraocular skeletal muscle development biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal extraocular muscle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extraocular muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
extraocular skeletal muscle development Gene Set From GO Biological Process Annotations 2025 genes participating in the extraocular skeletal muscle development biological process from the curated GO Biological Process Annotations 2025 dataset.
Myopathy of extraocular muscle Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extraocular retinoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extraocular retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extraocular muscle Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Extraocular muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Extraocular muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Extraocular muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
muscles Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term muscles in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
DMD_Deficiency_GDS2996_613_mouse_Cardiac muscles from 8-week (mdx animals) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DMD_Deficiency_GDS2996_613_mouse_Cardiac muscles from 8-week (mdx animals) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
DMD_Deficiency_GDS2996_614_mouse_Cardiac muscles from 10.5-month (mdx animals) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DMD_Deficiency_GDS2996_614_mouse_Cardiac muscles from 10.5-month (mdx animals) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PPARGC1B_Hypomorphic Mutation_GDS2515_695_mouse_Skeletal muscle - (quadriceps muscles) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PPARGC1B_Hypomorphic Mutation_GDS2515_695_mouse_Skeletal muscle - (quadriceps muscles) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
DES_KO_GDS4804_171_mouse_young skeletal muscles Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DES_KO_GDS4804_171_mouse_young skeletal muscles gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PPARalpha_OE_GDS2289_244_mouse_Skeletal muscles Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PPARalpha_OE_GDS2289_244_mouse_Skeletal muscles gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set From HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles 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.
paresis of extensor muscles of the big toe Gene Set From HPO Gene-Disease Associations genes associated with the paresis of extensor muscles of the big toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spasticity of pharyngeal muscles Gene Set From HPO Gene-Disease Associations genes associated with the spasticity of pharyngeal muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spasticity of facial muscles Gene Set From HPO Gene-Disease Associations genes associated with the spasticity of facial muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
firm muscles Gene Set From HPO Gene-Disease Associations genes associated with the firm muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness of long finger extensor muscles Gene Set From HPO Gene-Disease Associations genes associated with the weakness of long finger extensor muscles 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.
weakness of muscles of respiration Gene Set From HPO Gene-Disease Associations genes associated with the weakness of muscles of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased collagen deposition in the muscles Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities 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.
Masticatory Muscles, Hypertrophy Of Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Masticatory Muscles, Hypertrophy Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Floppy Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Floppy Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Neck Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Neck Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Bulbar Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Bulbar Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Distal Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Distal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Respiratory Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Respiratory Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatiguable Weakness Of Proximal Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatiguable Weakness Of Proximal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Weakness Of Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Weakness Of Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Muscle Weakness Of Muscles Innervated By Cn Vii Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Muscle Weakness Of Muscles Innervated By Cn Vii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Of Long Finger Extensor Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Long Finger Extensor Muscles 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.
Spasticity Of Facial Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spasticity Of Facial Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spasticity Of Pharyngeal Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spasticity Of Pharyngeal Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Swallowing Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Swallowing Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Jaw Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Jaw Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Skeletal Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Skeletal Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Firm Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Firm Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Of Muscles Of Respiration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Muscles Of Respiration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Speech Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Speech Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
increased collagen deposition in the muscles Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent eye muscles Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
congenital heart defects; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome 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.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart Defects, Congenital, And Other Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cystic fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oral Submucous Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oral Submucous Fibrosis from the curated CTD Gene-Disease Associations dataset.
Peritoneal Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peritoneal Fibrosis from the curated CTD Gene-Disease Associations dataset.
Endomyocardial Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Endomyocardial Fibrosis from the curated CTD Gene-Disease Associations dataset.
Pulmonary Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.
Cystic Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cystic Fibrosis from the curated CTD Gene-Disease Associations dataset.
CYSTIC FIBROSIS, MODIFIER OF, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CYSTIC FIBROSIS, MODIFIER OF, 1 from the curated CTD Gene-Disease Associations dataset.
Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.
Cystic Fibrosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Cystic Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
cystic fibrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cystic fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cystic fibrosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cystic fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pulmonary fibrosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pulmonary fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
cystic fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cystic fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
oral submucous fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oral submucous fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diffuse pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diffuse pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
localized pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease localized pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
endomyocardial fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endomyocardial fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
preretinal fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease preretinal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholestasis, intrahepatic; fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; infertility, male; oligospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; ileus; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; ileus; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; lung diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; lung diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung neoplasms; neoplasm of lung ; pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lung neoplasms; neoplasm of lung ; pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary fibrosis; pigeon breeders disease Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; pigeon breeders disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; fibrosis; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; fibrosis; iron overload 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.
pulmonary fibrosis; sarcoidosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; diabetes mellitus, type 1; hyperglycemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes mellitus, type 1; hyperglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; candida Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; candida in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colonic diseases; cystic fibrosis; Gene Set From GAD Gene-Disease Associations genes associated with the disease colonic diseases; cystic fibrosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; dna damage Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chemotherapy-induced pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chemotherapy-induced pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis c, chronic; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; pseudomonas infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; lung diseases; pseudomonas infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; lung diseases; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatic iron and fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatic iron and fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; exocrine pancreatic insufficiency; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis lung disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis lung disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary fibrosis; sarcoidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; rhinitis; sinusitis Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; ileus Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; disease susceptibility; pseudomonas infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; disease susceptibility; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; retroperitoneal fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; retroperitoneal fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary fibrosis; scleroderma, systemic Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; pancreatitis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; intussusception Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; intussusception in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever 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.
breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; respiratory tract diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung allograft fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lung allograft fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; disease models, animal; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; disease models, animal; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis c Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cystic fibrosis; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; diabetes complications Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; fibrosis; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; fibrosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; urogenital abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary fibrosis; scleroderma, systemic; systemic scleroderma Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; scleroderma, systemic; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
azoospermia; cystic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease azoospermia; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; protein-energy malnutrition Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; protein-energy malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; cystic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; maxillary sinusitis; sinusitis, maxillary Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; maxillary sinusitis; sinusitis, maxillary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis c, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; diabetes mellitus; pseudomonas infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes mellitus; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis b, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis b, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood pressure, arterial; cystic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
clonorchiasis; fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease clonorchiasis; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd 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.
cystic fibrosis; pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases, interstitial; pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases, interstitial; pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cystic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; steatorrhea Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; lung diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; lung diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oral submucous fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; pancreatitis, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oral submucous fibrosis; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease oral submucous fibrosis; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burkholderia infections; cystic fibrosis; pseudomonas infections Gene Set From GAD Gene-Disease Associations genes associated with the disease burkholderia infections; cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; neoplasms; radiation injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis c, chronic; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; dental caries Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; dental caries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; paranasal sinus diseases; sinus Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; paranasal sinus diseases; sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aspergillosis; cystic fibrosis; lung diseases, fungal Gene Set From GAD Gene-Disease Associations genes associated with the disease aspergillosis; cystic fibrosis; lung diseases, fungal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; gastrointestinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hcv-induced liver fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hcv-induced liver fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; growth disorders; nutrition disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; growth disorders; nutrition disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; cystic fibrosis; ileus Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; p. aeruginosa infection Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; p. aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases 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.
breast neoplasms; fibrosis; mammary neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; fibrosis; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; exocrine pancreatic insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis; lung diseases, interstitial; scleroderma, systemic Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrosis; lung diseases, interstitial; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oral cancer; oral submucous fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease oral cancer; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrosis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term fibrosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Cystic fibrosis severity Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hepatitis C induced liver fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
cystic fibrosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cystic fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
pulmonary fibrosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the pulmonary fibrosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
tubulointerstitial fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the tubulointerstitial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pancreatic fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the pancreatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myocardial fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the myocardial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulmonary fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the pulmonary fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
arterial intimal fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the arterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
portal fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the portal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hepatic fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retroperitoneal fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the retroperitoneal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
perifollicular fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the perifollicular fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
endocardial fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the endocardial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
periportal fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the periportal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulmonary aterial intimal fibrosis Gene Set From HPO Gene-Disease Associations genes associated with the pulmonary aterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Oral Submucous Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Oral Submucous Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pulmonary Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cystic Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cystic Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retroperitoneal Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retroperitoneal Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cystic fibrosis transmembrane conductance regulator Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cystic fibrosis transmembrane conductance regulator protein domain from the InterPro Predicted Protein Domain Annotations dataset.
retinal fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cardiac interstitial fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cardiac fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cardiac fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreas fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
liver fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the liver fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spleen fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spleen fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
perivascular fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the perivascular fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
urinary bladder fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the urinary bladder fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle interstitial fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal interstitial fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle endomysial fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary interstitial fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set From OMIM Gene-Disease Associations genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary fibrosis, telomere-related, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, telomere-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
cystic fibrosis Gene Set From OMIM Gene-Disease Associations genes associated with the cystic fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary fibrosis, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
{pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} Gene Set From OMIM Gene-Disease Associations genes associated with the {pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary fibrosis, idiopathic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{cystic fibrosis lung disease, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {cystic fibrosis lung disease, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{meconium ileus in cystic fibrosis, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {meconium ileus in cystic fibrosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
fibrosis Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term fibrosis in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
cystic fibrosis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease cystic fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis, Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oral Submucous Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oral Submucous Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peritoneal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peritoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Interstitial Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Interstitial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Combined Pulmonary Fibrosis And Emphysema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Combined Pulmonary Fibrosis And Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Fibrosis And Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Fibrosis And Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Pleura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pleura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Fibrosis - From Asbestos Exposure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis - From Asbestos Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arterial Intimal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arterial Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Aterial Intimal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Aterial Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nephrogenic Systemic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nephrogenic Systemic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Retroperitoneal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Retroperitoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Classical Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Classical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystic Fibrosis In Children Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystic Fibrosis Related Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis Related Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystic Fibrosis With Meconium Ileus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis With Meconium Ileus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Liver Disease Associated With Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Liver Disease Associated With Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sweat Chloride Elevation Without Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sweat Chloride Elevation Without Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Urinary Bladder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Urinary Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arterial Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arterial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intimal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oesophageal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oesophageal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Corpus Cavernosum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Corpus Cavernosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis, Neurodegeneration, And Cerebral Angiomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Neurodegeneration, And Cerebral Angiomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystic Fibrosis Modifier 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis Modifier 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prostatic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Portal Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Portal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubulointerstitial Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubulointerstitial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intestinal Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intestinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Endomyocardial Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endomyocardial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Periportal Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periportal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Skeletal Muscle Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibrosis Of Mesentery Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Mesentery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Myocardial Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myocardial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Perifollicular Fibrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perifollicular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
pulmonary fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreas fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cardiac fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal interstitial fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cardiac interstitial fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
liver fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the liver fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle interstitial fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle endomysial fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skin fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skin fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
urinary bladder fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the urinary bladder fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pulmonary interstitial fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal glomerulus fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
perivascular fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the perivascular fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spleen fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spleen fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
trachea fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the trachea fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ovary fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intestinal fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epididymis fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
uterus fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the uterus fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Idiopathic pulmonary fibrosis cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Lung fibrosis Gene Set From WikiPathways Pathways 2024 proteins participating in the Lung fibrosis pathway from the WikiPathways Pathways 2024 dataset.
HIPK2 in kidney fibrosis Gene Set From WikiPathways Pathways 2024 proteins participating in the HIPK2 in kidney fibrosis pathway from the WikiPathways Pathways 2024 dataset.
Nitric oxide metabolism in cystic fibrosis Gene Set From WikiPathways Pathways 2024 proteins participating in the Nitric oxide metabolism in cystic fibrosis pathway from the WikiPathways Pathways 2024 dataset.
Defective CFTR causes cystic fibrosis Gene Set From Reactome Pathways 2024 proteins participating in the Defective CFTR causes cystic fibrosis pathway from the Reactome Pathways 2024 dataset.
Cystic fibrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cystic fibrosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cystic fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cystic fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oral submucous fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oral submucous fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Preretinal fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Preretinal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Endomyocardial fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endomyocardial fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Postinflammatory pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Postinflammatory pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diffuse pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Localized pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Localized pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic pulmonary fibrosis disease specific cell type Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Idiopathic pulmonary fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cystic fibrosis disease specific cell type Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cystic fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Periportal fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Periportal fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cystic fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary fibrosis and/or bone marrow failure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis and/or bone marrow failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic Pulmonary Fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic Pulmonary Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cystic fibrosis-gastritis-megaloblastic anemia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis-gastritis-megaloblastic anemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse interstitial pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse interstitial pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary fibrosis and/or bone marrow failure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis and/or bone marrow failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hepatorenocardiac degenerative fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatorenocardiac degenerative fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Meconium ileus in cystic fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meconium ileus in cystic fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver fibrosis and steatohepatitis severity (MRI cT1 measure) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis and steatohepatitis severity (MRI cT1 measure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lung disease severity in cystic fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung disease severity in cystic fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver fibrosis severity in HIV/hepatitis C co-infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis severity in HIV/hepatitis C co-infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver fibrosis in pediatric non-alcoholic fatty acid liver disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis in pediatric non-alcoholic fatty acid liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver fibrosis (total hepatic collagen content) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis (total hepatic collagen content) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cystic fibrosis-related diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cystic fibrosis-related diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hepatitis C induced liver fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver fibrosis in non-alcoholic fatty liver disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cystic fibrosis severity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hyperplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital human immunodeficiency virus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital human immunodeficiency virus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diarrhea 5, with tufting enteropathy, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 5, with tufting enteropathy, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vertical talus, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vertical talus, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IV, congenital neuromuscular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial paresis, hereditary congenital, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital glucose-galactose malabsorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with cores Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aphakia, congenital primary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital contractural arachnodactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital contractural arachnodactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nystagmus 6, congenital, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Afibrinogenemia, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Afibrinogenemia, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diarrhea 3, secretory sodium, congenital, syndromic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 3, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hypoplasia, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital secretory diarrhea, chloride type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Indifference to pain, congenital, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart defects, multiple types, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital erythropoietic porphyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital erythropoietic porphyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with excess of thin myofilaments Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, with excess of muscle spindles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal recessive form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 6, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency 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.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, compton-north Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital cystic disease of liver Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver 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.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital order of glycosylation type 1r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital central hypoventilation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital ocular coloboma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital ocular coloboma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital clubbing, isolated congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1t Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prothrombin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital aniridia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital aniridia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital hyperammonemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital exostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamine deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Partial congenital absence of teeth Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Partial congenital absence of teeth phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myasthenic syndrome, acetazolamide-responsive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myasthenic syndrome, acetazolamide-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glaucoma, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glaucoma, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Stromal Corneal Dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myopathy with fiber type disproportion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Hyperinsulinism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hyperinsulinism from the curated CTD Gene-Disease Associations dataset.
Cataract congenital Volkmann type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
Congenital bilateral aplasia of vas deferens Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.
Congenital Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Abnormalities from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic, Congenital Nonspherocytic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 4 from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 4 from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.
Congenital idiopathic intestinal pseudoobstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.
Vertical talus, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vertical talus, congenital from the curated CTD Gene-Disease Associations dataset.
Nystagmus 1, congenital, X- linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.
Facial paresis, hereditary, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset.
Congenital anosmia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital anosmia from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 5 from the curated CTD Gene-Disease Associations dataset.
Hyperferritinemia, hereditary, with congenital cataracts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.
Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Hernias, Diaphragmatic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hernias, Diaphragmatic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.
Lethal Congenital Contracture Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Aphakia, congenital primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aphakia, congenital primary 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.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Nystagmus 2, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 2, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 3 from the curated CTD Gene-Disease Associations dataset.
Congenital contractural arachnodactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital contractural arachnodactyly from the curated CTD Gene-Disease Associations dataset.
Lactase Deficiency, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.
Nystagmus 4, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 4, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Indifference to Pain, Congenital, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Indifference to Pain, Congenital, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Ptosis, Hereditary Congenital 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset.
Pain Insensitivity, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pain Insensitivity, Congenital from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital amegakaryocytic thrombocytopenia from the curated CTD Gene-Disease Associations dataset.
Adrenal Hyperplasia, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal Hyperplasia, Congenital from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.
Anemia, Hypoplastic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.
Congenital hypertrichosis lanuginosa Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital hypertrichosis lanuginosa from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 10 from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 2 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, Compton-North Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 3 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder of Glycosylation, Type Io Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital central hypoventilation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type Im Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type In Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Zonular, with Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
Lethal congenital contracture syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Microcoria, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcoria, congenital from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 14 from the curated CTD Gene-Disease Associations dataset.
ADRENAL HYPOPLASIA, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.
Ptosis, Hereditary Congenital 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Diarrhea 4, Malabsorptive, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diarrhea 4, Malabsorptive, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.
CAPILLARY MALFORMATIONS, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CAPILLARY MALFORMATIONS, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.
Nephrosis, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephrosis, congenital from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
GLAUCOMA 3, PRIMARY CONGENITAL, C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLAUCOMA 3, PRIMARY CONGENITAL, C from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Merosin-Positive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.
Myopathies, Structural, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathies, Structural, Congenital from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Recessive Congenital 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Recessive Congenital 3 from the curated CTD Gene-Disease Associations dataset.
Congenital myasthenic syndrome with episodic apnea Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.
Preauricular Fistulae, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Preauricular Fistulae, Congenital from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis from the curated CTD Gene-Disease Associations dataset.
Lower Extremity Deformities, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lower Extremity Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
NYSTAGMUS 5, CONGENITAL, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NYSTAGMUS 5, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Night blindness, congenital stationary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night blindness, congenital stationary from the curated CTD Gene-Disease Associations dataset.
Sucrase-isomaltase deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sucrase-isomaltase deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Congenital myasthenic syndrome ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome ib from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.
Marie Unna congenital hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Marie Unna congenital hypotrichosis from the curated CTD Gene-Disease Associations dataset.
NYSTAGMUS 6, CONGENITAL, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NYSTAGMUS 6, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Nystagmus 3, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 3, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 12 from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 13 from the curated CTD Gene-Disease Associations dataset.
Congenital atransferrinemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital atransferrinemia from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked from the curated CTD Gene-Disease Associations dataset.
ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR from the curated CTD Gene-Disease Associations dataset.
RETT SYNDROME, CONGENITAL VARIANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RETT SYNDROME, CONGENITAL VARIANT from the curated CTD Gene-Disease Associations dataset.
Myasthenic syndrome, congenital, postsynaptic slow-channel Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic syndrome, congenital, postsynaptic slow-channel from the curated CTD Gene-Disease Associations dataset.
Nystagmus, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.
Myasthenic Syndromes, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic Syndromes, Congenital from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Congenital Stromal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 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.
PROTHROMBIN DEFICIENCY, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROTHROMBIN DEFICIENCY, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
LEBER CONGENITAL AMAUROSIS 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LEBER CONGENITAL AMAUROSIS 15 from the curated CTD Gene-Disease Associations dataset.
Diarrhea 3, Secretory Sodium, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diarrhea 3, Secretory Sodium, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.
Limb Deformities, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.
Pancreatic Agenesis, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pancreatic Agenesis, Congenital from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis congenital generalized X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.
Nail dysplasia, isolated congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nail dysplasia, isolated congenital 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.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Lethal Congenital Contractural Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Congenital Contractural Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.
Heart Defects, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.
Glaucoma 3, Primary Congenital, D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, Primary Congenital, D from the curated CTD Gene-Disease Associations dataset.
Glaucoma 3, Primary Congenital, A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, Primary Congenital, A from the curated CTD Gene-Disease Associations dataset.
Adrenal hyperplasia, congenital, type 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal hyperplasia, congenital, type 5 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Cataract, congenital, with microcornea or slight microphthalmia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, congenital, with microcornea or slight microphthalmia from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Lipoid congenital adrenal hyperplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid congenital adrenal hyperplasia from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
Myasthenic Syndrome, Congenital, Fast-Channel Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic Syndrome, Congenital, Fast-Channel from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.
Glutamine deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutamine deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Retinal Nonattachment, Nonsyndromic Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.
SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS from the curated CTD Gene-Disease Associations dataset.
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Woolly hair, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Woolly hair, congenital from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease of Heart, Lethal Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.
Diarrhea 5, With Tufting Enteropathy, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diarrhea 5, With Tufting Enteropathy, Congenital from the curated CTD Gene-Disease Associations dataset.
Afibrinogenemia congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Afibrinogenemia congenital from the curated CTD Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.
CATARACT, CONGENITAL OR JUVENILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT, CONGENITAL OR JUVENILE from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
Anemia, Dyserythropoietic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Dyserythropoietic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Recessive 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Recessive 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset.
Hyperostosis, Cortical, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperostosis, Cortical, Congenital from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Lmna-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.
congenital afibrinogenemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital afibrinogenemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital disorder of glycosylation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital heart disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital heart disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital diaphragmatic hernia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital diaphragmatic hernia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital dyserythropoietic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital dyserythropoietic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
severe congenital neutropenia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease severe congenital neutropenia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital hemolytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital hemolytic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital structural myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital structural myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital nervous system abnormality Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital hypoplastic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital hypoplastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital hypothyroidism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital hypothyroidism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital myasthenic syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital myasthenic syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
leber congenital amaurosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease leber congenital amaurosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital stationary night blindness Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital stationary night blindness from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital ichthyosiform erythroderma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital ichthyosiform erythroderma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
late congenital syphilis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease late congenital syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type ii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital intrinsic factor deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital intrinsic factor deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital structural myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital nervous system abnormality Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital afibrinogenemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital afibrinogenemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital granular cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital granular cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital hypogammaglobulinemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital hypogammaglobulinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital syphilis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
severe congenital neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease severe congenital neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital hypoplastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital hypoplastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital adrenal insufficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital adrenal insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital stationary night blindness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital stationary night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital ichthyosiform erythroderma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital ichthyosiform erythroderma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital nonspherocytic hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nonspherocytic hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital toxoplasmosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital toxoplasmosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital mesoblastic nephroma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital mesoblastic nephroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital heart disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital heart disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital dyserythropoietic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital dyserythropoietic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital epulis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital epulis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital nystagmus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital myasthenic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital myasthenic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital bile acid synthesis defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital diaphragmatic hernia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital diaphragmatic hernia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital fibrosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital aphakia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital aphakia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cellular congenital mesoblastic nephroma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cellular congenital mesoblastic nephroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary congenital glaucoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary congenital glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type i Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital hypothyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital hypothyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leber congenital amaurosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leber congenital amaurosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary congenital glaucoma Gene Set From GAD Gene-Disease Associations genes associated with the disease primary congenital glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glaucoma, primary open-angle; glaucoma, primary congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease glaucoma, primary open-angle; glaucoma, primary congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set From GAD Gene-Disease Associations genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital nuclear cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital nuclear cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital central hypoventilation syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital central hypoventilation syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
limb deformities, congenital; rothmund-thomson syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease limb deformities, congenital; rothmund-thomson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital neutropenia Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nephropathy, congenital obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease nephropathy, congenital obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chuvash-type congenital polycythemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chuvash-type congenital polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital adrenal hyperplasia (cah) Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital adrenal hyperplasia (cah) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
phenytoin-induced congenital malformations Gene Set From GAD Gene-Disease Associations genes associated with the disease phenytoin-induced congenital malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital cardiac malformations Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital cardiac malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; hyperandrogenism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; hyperandrogenism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital nephrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital nephrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip dislocation, congenital; joint instability Gene Set From GAD Gene-Disease Associations genes associated with the disease hip dislocation, congenital; joint instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital thrombotic thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital thrombotic thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dilatation, pathologic; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease dilatation, pathologic; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriovenous malformations; congenital arteriovenous malformation; hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital megacolon; enterocolitis; hirschsprung disease Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital megacolon; enterocolitis; hirschsprung disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital megacolon; hirschsprung disease Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital megacolon; hirschsprung disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glaucoma, primary congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease glaucoma, primary congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital intrinsic factor deficiency. Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital intrinsic factor deficiency. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set From GAD Gene-Disease Associations genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease ullrich congenital muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
toxoplasmosis, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease toxoplasmosis, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathies; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathies; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy; heart anomalies, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy; heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; adrenal gland neoplasms; adrenal hyperplasia, congenital; hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; adrenal gland neoplasms; adrenal hyperplasia, congenital; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital bilateral absence of the vas deferens Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital bilateral absence of the vas deferens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital abnormalities; Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital abnormalities; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart anomalies, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; heart septal defects, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital haptoglobin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital haptoglobin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioretinitis; toxoplasmosis, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioretinitis; toxoplasmosis, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; autoimmune diseases; opportunistic infections; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; autoimmune diseases; opportunistic infections; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital abnormalities; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital abnormalities; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
wilms' tumor and congenital male genitourinary malformation Gene Set From GAD Gene-Disease Associations genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital and subclinical hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital and subclinical hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late-onset congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease late-onset congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital ductus arteriosus aneurysm Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital ductus arteriosus aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital primary hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital primary hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital anomalies Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital anomalies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital sick sinus syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital sick sinus syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disease models, animal; ichthyosiform erythroderma, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease disease models, animal; ichthyosiform erythroderma, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital abnormalities; hypothyroidism; thyroid dysgenesis Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital abnormalities; hypothyroidism; thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital megacolon; hirschsprung disease; urea cycle disorders, inborn Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital megacolon; hirschsprung disease; urea cycle disorders, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ichthyosiform erythroderma, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease ichthyosiform erythroderma, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip dislocation, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease hip dislocation, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital anomalies; cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leber congenital amaurosis and a normal ocular phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease leber congenital amaurosis and a normal ocular phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital anomalies; renal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital anomalies; renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital athyreosis Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital athyreosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart anomalies, congenital; pulmonary hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital; pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital contractural arachnodactyly Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital contractural arachnodactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set From GAD Gene-Disease Associations genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital hypothyroidism; thyroid dysgenesis Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital hypothyroidism; thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene Set From GAD Gene-Disease Associations genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital goiter and defective tg synthesis. Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital goiter and defective tg synthesis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital polycythemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital polycythemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune-associated congenital heart block. Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune-associated congenital heart block. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leber congenital amaurosis/lca Gene Set From GAD Gene-Disease Associations genes associated with the disease leber congenital amaurosis/lca in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital uropathies Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital uropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital cataracts Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital cataracts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital hypothyroidism; cretinism Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital hypothyroidism; cretinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leber congenital amaurosis Gene Set From GAD Gene-Disease Associations genes associated with the disease leber congenital amaurosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term congenital in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Leber congenital amaurosis_Retina_GSE3249 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Leber congenital amaurosis_Retina_GSE3249 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Congenital heart malformation Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Congenital heart malformation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Congenital heart disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Congenital heart disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
congenital heart disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease congenital heart disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
congenital hemolytic anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease congenital hemolytic anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
congenital glaucoma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the congenital glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
primary congenital glaucoma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the primary congenital glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
congenital stapes ankylosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital stapes ankylosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital microcephaly Gene Set From HPO Gene-Disease Associations genes associated with the congenital microcephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive congenital scoliosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive congenital scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypoparathyroidism Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypoparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the congenital nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital neutropenia Gene Set From HPO Gene-Disease Associations genes associated with the congenital neutropenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital ptosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital ptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital primary aphakia Gene Set From HPO Gene-Disease Associations genes associated with the congenital primary aphakia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital bilateral hip dislocation Gene Set From HPO Gene-Disease Associations genes associated with the congenital bilateral hip dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital muscular torticollis Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular torticollis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital lactic acidosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital localized absence of skin Gene Set From HPO Gene-Disease Associations genes associated with the congenital localized absence of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
numerous congenital melanocytic nevi Gene Set From HPO Gene-Disease Associations genes associated with the numerous congenital melanocytic nevi phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital abnormal hair pattern Gene Set From HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital laryngeal stridor Gene Set From HPO Gene-Disease Associations genes associated with the congenital laryngeal stridor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital malformation of the great arteries Gene Set From HPO Gene-Disease Associations genes associated with the congenital malformation of the great arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital contracture Gene Set From HPO Gene-Disease Associations genes associated with the congenital contracture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital palmoplantar keratosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital palmoplantar keratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital myopia Gene Set From HPO Gene-Disease Associations genes associated with the congenital myopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the congenital sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital nystagmus Gene Set From HPO Gene-Disease Associations genes associated with the congenital nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital blindness Gene Set From HPO Gene-Disease Associations genes associated with the congenital blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital pseudoarthrosis of the clavicle Gene Set From HPO Gene-Disease Associations genes associated with the congenital pseudoarthrosis of the clavicle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypothyroidism Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital kyphoscoliosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital kyphoscoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypertrophy of left ventricle Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypertrophy of left ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital goiter Gene Set From HPO Gene-Disease Associations genes associated with the congenital goiter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive congenital retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital adrenal hyperplasia Gene Set From HPO Gene-Disease Associations genes associated with the congenital adrenal hyperplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital macroorchidism Gene Set From HPO Gene-Disease Associations genes associated with the congenital macroorchidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital stationary night blindness Gene Set From HPO Gene-Disease Associations genes associated with the congenital stationary night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital nephrotic syndrome Gene Set From HPO Gene-Disease Associations genes associated with the congenital nephrotic syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypertrophy of retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypertrophy of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital malformation of the right heart Gene Set From HPO Gene-Disease Associations genes associated with the congenital malformation of the right heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital posterior urethral valve Gene Set From HPO Gene-Disease Associations genes associated with the congenital posterior urethral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital nonbullous ichthyosiform erythroderma Gene Set From HPO Gene-Disease Associations genes associated with the congenital nonbullous ichthyosiform erythroderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital malformation of the left heart Gene Set From HPO Gene-Disease Associations genes associated with the congenital malformation of the left heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital cataract Gene Set From HPO Gene-Disease Associations genes associated with the congenital cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
primary congenital glaucoma Gene Set From HPO Gene-Disease Associations genes associated with the primary congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hemolytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the congenital hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital onychodystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital onychodystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital ichthyosiform erythroderma Gene Set From HPO Gene-Disease Associations genes associated with the congenital ichthyosiform erythroderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hip dislocation Gene Set From HPO Gene-Disease Associations genes associated with the congenital hip dislocation 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.
late onset congenital glaucoma Gene Set From HPO Gene-Disease Associations genes associated with the late onset congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital thrombocytopenia Gene Set From HPO Gene-Disease Associations genes associated with the congenital thrombocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital septal defect Gene Set From HPO Gene-Disease Associations genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital agranulocytosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital agranulocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital finger flexion contractures Gene Set From HPO Gene-Disease Associations genes associated with the congenital finger flexion contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital giant melanocytic nevus Gene Set From HPO Gene-Disease Associations genes associated with the congenital giant melanocytic nevus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital strabismus Gene Set From HPO Gene-Disease Associations genes associated with the congenital strabismus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypoplastic anemia Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypoplastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital glaucoma Gene Set From HPO Gene-Disease Associations genes associated with the congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital bullous ichthyosiform erythroderma Gene Set From HPO Gene-Disease Associations genes associated with the congenital bullous ichthyosiform erythroderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital symmetrical palmoplantar keratosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital symmetrical palmoplantar keratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital, generalized hypertrichosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital, generalized hypertrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital diaphragmatic hernia Gene Set From HPO Gene-Disease Associations genes associated with the congenital diaphragmatic hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital pyloric atresia Gene Set From HPO Gene-Disease Associations genes associated with the congenital pyloric atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital onset Gene Set From HPO Gene-Disease Associations genes associated with the congenital onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Congenital Hypothyroidism Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Congenital Hypothyroidism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Congenital Hyperinsulinism Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Congenital Hyperinsulinism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Congenital Abnormalities Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Congenital Abnormalities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Anemia, Hemolytic, Congenital Nonspherocytic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Anemia, Hemolytic, Congenital Nonspherocytic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pain Insensitivity, Congenital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pain Insensitivity, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Anemia, Hemolytic, Congenital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Anemia, Hemolytic, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Harmonizome 3.0

congenital fibrosis of the extraocular muscles Gene Set

Congenital Fibrosis Of The Extraocular Muscles Gene Set

Congenital fibrosis of the extraocular muscles Gene Set

Congenital fibrosis of the extraocular muscles Gene Set

Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set

Fibrosis of extraocular muscles, congenital, 3b Gene Set

Fibrosis of extraocular muscles, congenital, 2 Gene Set

Fibrosis of extraocular muscles, congenital, 1 Gene Set

Fibrosis of Extraocular Muscles, Congenital, 3B Gene Set

Fibrosis Of Extraocular Muscles, Congenital, 2 Gene Set

congenital fibrosis of extraocular muscles type 2 Gene Set

congenital fibrosis of extraocular muscles Gene Set

fibrosis of extraocular muscles, congenital, 2 Gene Set

fibrosis of extraocular muscles, congenital, 1 Gene Set

fibrosis of extraocular muscles, congenital, 3b Gene Set

fibrosis of extraocular muscles, congenital, 3a Gene Set

Congenital fibrosis of the extraocular muscles 1 Gene Set

Congenital fibrosis of the extraocular muscles 3A Gene Set

Congenital fibrosis of extraocular muscles Gene Set

Fibrosis Of Extraocular Muscles Gene Set

Fibrosis Of Extraocular Muscles Gene Set

Fibrosis of extraocular muscles Gene Set

abnormality of the extraocular muscles Gene Set

Abnormality Of The Extraocular Muscles Gene Set

Weak Extraocular Muscles Gene Set

absent extraocular muscles Gene Set

fibrosis; pulmonary fibrosis; scleroderma, systemic Gene Set

congenital hepatic fibrosis Gene Set

Hepatic Fibrosis, Congenital Gene Set

myopathy of extraocular muscle Gene Set

myopathy of extraocular muscle Gene Set

extraocular retinoblastoma Gene Set

extraocular Gene Set

extraocular skeletal muscle development Gene Set

limited extraocular movements Gene Set

abnormal extraocular muscle morphology Gene Set

extraocular muscle Gene Set

extraocular muscle Gene Set

Extraocular Retinoblastoma Gene Set

Extraocular Muscle Paresis Gene Set

Limited Extraocular Movements Gene Set

Abnormality Of Inferior Oblique Extraocular Muscle Gene Set

extraocular skeletal muscle development Gene Set

abnormal extraocular muscle morphology Gene Set

extraocular skeletal muscle development Gene Set

Myopathy of extraocular muscle Gene Set

Extraocular retinoblastoma Gene Set

Extraocular muscle Gene Set

Extraocular muscle Gene Set

muscles Gene Set

DMD_Deficiency_GDS2996_613_mouse_Cardiac muscles from 8-week (mdx animals) Gene Set

DMD_Deficiency_GDS2996_614_mouse_Cardiac muscles from 10.5-month (mdx animals) Gene Set

PPARGC1B_Hypomorphic Mutation_GDS2515_695_mouse_Skeletal muscle - (quadriceps muscles) Gene Set

DES_KO_GDS4804_171_mouse_young skeletal muscles Gene Set

PPARalpha_OE_GDS2289_244_mouse_Skeletal muscles Gene Set

decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set

hypotrophy of the small hand muscles Gene Set

paresis of extensor muscles of the big toe Gene Set

spasticity of pharyngeal muscles Gene Set

spasticity of facial muscles Gene Set

firm muscles Gene Set

weakness of long finger extensor muscles Gene Set

weakness of the intrinsic hand muscles Gene Set

weakness of muscles of respiration Gene Set

increased collagen deposition in the muscles Gene Set

Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene Set

Hypotrophy Of The Small Hand Muscles Gene Set

Masticatory Muscles, Hypertrophy Of Gene Set

Floppy Muscles Gene Set

Fatigable Weakness Of Neck Muscles Gene Set

Fatigable Weakness Of Bulbar Muscles Gene Set

Fatigable Weakness Of Distal Limb Muscles Gene Set

Fatigable Weakness Of Respiratory Muscles Gene Set

Fatiguable Weakness Of Proximal Limb Muscles Gene Set

Generalized Weakness Of Limb Muscles Gene Set

Facial Muscle Weakness Of Muscles Innervated By Cn Vii Gene Set

Weakness Of Long Finger Extensor Muscles Gene Set

Weakness Of The Intrinsic Hand Muscles Gene Set