developmental dysplasia of the hip 2

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Results for "developmental dysplasia of the hip 2": 1002 gene sets

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developmental dysplasia of the hip 2 Gene Set From OMIM Gene-Disease Associations genes associated with the developmental dysplasia of the hip 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Developmental dysplasia of the hip 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental dysplasia of the hip 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
DEVELOPMENTAL DYSPLASIA OF THE HIP 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEVELOPMENTAL DYSPLASIA OF THE HIP 1 from the curated CTD Gene-Disease Associations dataset.
Developmental Dysplasia Of The Hip 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Dysplasia Of The Hip 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental dysplasia of the hip Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental dysplasia of the hip in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental dysplasia of the hip 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental dysplasia of the hip 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental dysplasia of the hip Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental dysplasia of the hip phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental dysplasia of the hip Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental dysplasia of the hip phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
degenerative arthropathy ; hip fractures; osteoarthritis; osteoarthritis, hip; osteoarthritis, knee; osteoporosis Gene Set From GAD Gene-Disease Associations genes associated with the disease degenerative arthropathy ; hip fractures; osteoarthritis; osteoarthritis, hip; osteoarthritis, knee; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip fractures; osteoarthritis, hip Gene Set From GAD Gene-Disease Associations genes associated with the disease hip fractures; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone diseases, developmental; osteoarthritis, hip Gene Set From GAD Gene-Disease Associations genes associated with the disease bone diseases, developmental; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Hip Dysplasia, Beukes Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hip Dysplasia, Beukes Type from the curated CTD Gene-Disease Associations dataset.
osteoarthritis; hip dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoarthritis; hip dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the hip dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hip dysplasia, beukes type Gene Set From OMIM Gene-Disease Associations genes associated with the hip dysplasia, beukes type phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Dysplasia Of The Hip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Dysplasia Of The Hip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Namaqualand Hip Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Namaqualand Hip Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Dysplasia, Beukes Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Dysplasia, Beukes Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Dysplasia, Congenital, Nonsyndromic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Dysplasia, Congenital, Nonsyndromic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Beukes hip dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Beukes hip dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Namaqualand hip dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Namaqualand hip dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hip dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hip dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteoarthritis, Hip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteoarthritis, Hip from the curated CTD Gene-Disease Associations dataset.
Hip Fractures Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hip Fractures from the curated CTD Gene-Disease Associations dataset.
Hip Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Hip in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Waist-Hip Ratio Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Waist-Hip Ratio in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
osteoarthritis, hip; osteoarthritis, knee Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoarthritis, hip; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
waist-hip ratio Gene Set From GAD Gene-Disease Associations genes associated with the disease waist-hip ratio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip bone loss and fracture Gene Set From GAD Gene-Disease Associations genes associated with the disease hip bone loss and fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip fractures; osteoporosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hip fractures; osteoporosis 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.
fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
osteoarthritis, hip Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
osteoarthritis; osteoarthritis, hip; osteoarthritis, knee Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoarthritis; osteoarthritis, hip; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease hip fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip geometry Gene Set From GAD Gene-Disease Associations genes associated with the disease hip geometry 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.
hip fractures; osteoporosis, postmenopausal Gene Set From GAD Gene-Disease Associations genes associated with the disease hip fractures; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthralgia; osteoarthritis, hip Gene Set From GAD Gene-Disease Associations genes associated with the disease arthralgia; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone mineral density (hip) Gene Set From GAD Gene-Disease Associations genes associated with the disease bone mineral density (hip) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip Gene Set From GAD Gene-Disease Associations genes associated with the disease hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip bone size Gene Set From GAD Gene-Disease Associations genes associated with the disease hip bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hip in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Hip bone size Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hip bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bone mineral density (hip) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bone mineral density (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Waist-hip ratio Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Waist-hip ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Osteoarthritis (hip) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Osteoarthritis (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Waist-to-hip circumference ratio (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Waist-to-hip circumference ratio (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hip geometry Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hip geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
hip osteoarthritis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the hip osteoarthritis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the hip bone Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the hip joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the hip joint 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.
hip osteoarthritis Gene Set From HPO Gene-Disease Associations genes associated with the hip osteoarthritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited hip movement Gene Set From HPO Gene-Disease Associations genes associated with the limited hip movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the hip bone Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the hip bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hip contracture Gene Set From HPO Gene-Disease Associations genes associated with the hip contracture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the hip-girdle musculature Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the hip-girdle musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited hip extension Gene Set From HPO Gene-Disease Associations genes associated with the limited hip extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
arthralgia of the hip Gene Set From HPO Gene-Disease Associations genes associated with the arthralgia of the hip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased hip abduction Gene Set From HPO Gene-Disease Associations genes associated with the decreased hip abduction 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.
hip dislocation Gene Set From HPO Gene-Disease Associations genes associated with the hip dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Osteoarthritis, Hip Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Osteoarthritis, Hip phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hip Dislocation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hip Dislocation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hip Fractures Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hip Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hip Dislocation, Congenital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hip Dislocation, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hip Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
hip joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hip joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Hip Pain Chronic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Pain Chronic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Contracture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Contracture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Hip Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Hip Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Congenital Dislocation Of Hip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Congenital Dislocation Of Hip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Dislocation, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Dislocation, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Flexion Contracture Of Hip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Flexion Contracture Of Hip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Hip Joint Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Hip Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyogenic Arthritis Of Hip Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyogenic Arthritis Of Hip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Waist-Hip Ratio Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Waist-Hip Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Waist To Hip Ratio Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Waist To Hip Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Joint Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Joint Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Joint Varus Deformity - Observation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Joint Varus Deformity - Observation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Circumference Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Circumference in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Waist To Hip Ratio Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Waist To Hip Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Flexor Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Telescoping Of Limb At Hip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Telescoping Of Limb At Hip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Hip Abduction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Hip Abduction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Hip Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Hip Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Hip Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Hip Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postoperative Hip Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Hip Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Stiff Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Stiff in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Transient Osteoporosis Of Hip Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Osteoporosis Of Hip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
hip dislocation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hip dislocation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hip joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hip joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Hip joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hip joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Hip Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Congenital hip dislocation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital hip dislocation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hip flexor weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hip flexor weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Serum C-reactive protein concentration in visceral obesity (waist-hip ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum C-reactive protein concentration in visceral obesity (waist-hip ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral density (total hip) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (total hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral density (hip) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral density (hip) and age at menarche Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (hip) and age at menarche phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for body mass index Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thoracic-to-hip circumference ratio Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic-to-hip circumference ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Low bone mineral density (hip) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low bone mineral density (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis (with total hip replacement) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis (with total hip replacement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric bone mineral density (hip) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral density (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip circumference adjusted for BMI Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip circumference adjusted for BMI phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis (hip) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis of the hip or knee Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis of the hip or knee phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and HDL-C (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and HDL-C (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and LDL-C (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and LDL-C (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and triglycerides (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and triglycerides (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and systolic blood pressure (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and systolic blood pressure (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and coronary artery disease (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and coronary artery disease (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip ratio and type 2 diabetes (pairwise) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and type 2 diabetes (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip circumference (psychosocial stress interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip circumference (psychosocial stress interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip circumference ratio (ever vs never smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (ever vs never smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip circumference ratio (dietary energy interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (dietary energy interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip circumference ratio (smoking years interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (smoking years interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip circumference ratio (recreational physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (recreational physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip circumference ratio (alcohol intake interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip circumference Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip circumference phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip shape (DXA scan) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip shape (DXA scan) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip bone mineral density and total body fat mass (bivariate analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip bone mineral density and total body fat mass (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (recessive genetic model) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (recessive genetic model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (additive genetic model) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (additive genetic model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip bone size Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip geometry Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip minimal joint space width Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip minimal joint space width phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis of the hip or knee (with total joint replacement) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis of the hip or knee (with total joint replacement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index and waist-hip ratio (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and waist-hip ratio (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip index Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-hip index Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI in non-smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI in non-smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI in smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI in smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (adjusted for smoking behaviour) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (adjusted for smoking behaviour) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (joint analysis for main effect and physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (joint analysis for main effect and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI in active individuals Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI in active individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (age <50) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (age <50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (age >50) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (age >50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI in inactive individuals Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI in inactive individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and waist-to-hip-ratio (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and waist-to-hip-ratio (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip circumference variance Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip circumference variance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death 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.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Developmental Disabilities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Developmental Disabilities from the curated CTD Gene-Disease Associations dataset.
Bone Diseases, Developmental Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Developmental from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY 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.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.
pervasive developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pervasive developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease specific developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease developmental disorder of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease specific developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pervasive developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pervasive developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental coordination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease specific developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anodontia; developmental absence of tooth Gene Set From GAD Gene-Disease Associations genes associated with the disease anodontia; developmental absence of tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
developmental Gene Set From GAD High Level Gene-Disease Associations genes associated with the disease developmental in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.
developmental Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term developmental in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
developmental maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental growth involved in morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental growth involved in morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
single-organism developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the single-organism developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental cell growth Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental cell growth biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
pigment metabolic process involved in developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the pigment metabolic process involved in developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental induction Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental induction biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental process involved in reproduction Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental process involved in reproduction biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
spongiotrophoblast layer developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the spongiotrophoblast layer developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
specific developmental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease specific developmental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
developmental disorder of mental health Gene Set From GWASdb SNP-Disease Associations genes associated with the disease developmental disorder of mental health in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
pervasive developmental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease pervasive developmental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
developmental stagnation Gene Set From HPO Gene-Disease Associations genes associated with the developmental stagnation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
moderate global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the moderate global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
developmental stagnation at onset of seizures Gene Set From HPO Gene-Disease Associations genes associated with the developmental stagnation at onset of seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
developmental regression Gene Set From HPO Gene-Disease Associations genes associated with the developmental regression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the severe global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Developmental Disabilities Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Developmental Disabilities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bone Diseases, Developmental Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bone Diseases, Developmental phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Developmental pluripotency-associated protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 2/4, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sox developmental protein N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sox developmental protein N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 2/4, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interferon-related developmental regulator, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interferon-related developmental regulator, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interferon-related developmental regulator, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interferon-related developmental regulator, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal developmental patterning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal developmental patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal developmental vascular remodeling Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal developmental vascular remodeling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
obesity, hyperphagia, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, seizures, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, seizures, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
?obesity, hyperphagia, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the ?obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
growth retardation, developmental delay, coarse facies, and early death Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.
sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
developmental Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term developmental in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Developmental Biology Gene Set From Reactome Pathways 2014 proteins participating in the Developmental Biology pathway from the Reactome Pathways dataset.
Developmental Regression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Global Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Coordination Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Coordination Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Reading Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Reading Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Global Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Arithmetic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Arithmetic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Absence Of Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Absence Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brachycephaly, Trichomegaly, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brachycephaly, Trichomegaly, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intellectual Developmental Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intellectual Developmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phonological Developmental Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phonological Developmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lateral Developmental Cyst Of Jaw Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lateral Developmental Cyst Of Jaw in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Porencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Porencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Failure Of Fusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Failure Of Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Coxa Vara Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Coxa Vara in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Communication Disorders, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Communication Disorders, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Valvular Defect, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Valvular Defect, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Syntactic Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Syntactic Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental And Speech Delay Due To Sox5 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental And Speech Delay Due To Sox5 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Plantar Lipomatosis, Unusual Facies, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Plantar Lipomatosis, Unusual Facies, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac, Facial, And Digital Anomalies With Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac, Facial, And Digital Anomalies With Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay (Disorder) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Delay (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Stagnation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Stagnation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Academic Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Academic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Moderate Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderate Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Stagnation At Onset Of Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Stagnation At Onset Of Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Symptoms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pili Torti Developmental Delay Neurological Abnormalities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pili Torti Developmental Delay Neurological Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Delay, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Delay, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Developmental Milestones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Developmental Milestones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of developmental growth Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of developmental growth biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of developmental growth Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of developmental growth biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of developmental growth Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of developmental growth biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of developmental process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of developmental process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of developmental process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of developmental process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal developmental patterning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal developmental patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
developmental cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the developmental cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal developmental vascular remodeling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal developmental vascular remodeling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
behavioral developmental delay Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the behavioral developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
motor developmental delay Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the motor developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Developmental Biology Gene Set From Reactome Pathways 2024 proteins participating in the Developmental Biology pathway from the Reactome Pathways 2024 dataset.
Developmental Cell Lineages Gene Set From Reactome Pathways 2024 proteins participating in the Developmental Cell Lineages pathway from the Reactome Pathways 2024 dataset.
Disorders of Developmental Biology Gene Set From Reactome Pathways 2024 proteins participating in the Disorders of Developmental Biology pathway from the Reactome Pathways 2024 dataset.
Pervasive developmental disorders Gene Set From Reactome Pathways 2024 proteins participating in the Pervasive developmental disorders pathway from the Reactome Pathways 2024 dataset.
positive regulation of developmental growth Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of developmental growth biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of developmental growth Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of developmental growth biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of developmental growth Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of developmental growth biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of developmental process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of developmental process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of developmental process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of developmental process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental disorder of mental health from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Pervasive developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pervasive developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Specific developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Specific developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 14 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 29 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 13 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
microcephaly, seizures, and developmental delay Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease microcephaly, seizures, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 26 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 109 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked intellectual developmental disorder 109 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 43 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Specific developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Specific developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Pervasive developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pervasive developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Specific developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Specific developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pervasive developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pervasive developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 86 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 86 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
microcephaly, seizures, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease microcephaly, seizures, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 84 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 80 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 80 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental coordination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 93 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 93 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 53 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 53 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 76 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental delay and seizures with or without movement abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay and seizures with or without movement abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with short stature and behavioral abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with short stature and behavioral abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 98 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 98 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 108 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual developmental disorder 108 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital limbs-face contractures-hypotonia-developmental delay syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital limbs-face contractures-hypotonia-developmental delay syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with cardiac arrhythmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with cardiac arrhythmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 31A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 31A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 60 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 60 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 62 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 62 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 103 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 103 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 91 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 91 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 66 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 66 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 109 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual developmental disorder 109 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 87 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 94 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 94 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 6B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 6B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 65 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 65 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental cardiac valvular defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental cardiac valvular defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual developmental disorder bain type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual developmental disorder bain type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 99 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 97 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 97 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 75 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 102 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 102 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
brachycephaly, trichomegaly, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease brachycephaly, trichomegaly, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 82 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 85 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 85 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 59 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 59 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 67 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 67 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 104 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 104 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 106 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 106 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 74 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 74 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 58 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 58 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 90 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 90 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 57 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual developmental disorder 111 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual developmental disorder 111 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 72 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 72 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 71 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 71 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 100 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 100 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 96 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 96 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 89 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 89 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with ocular anomalies and distinctive facial features Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with ocular anomalies and distinctive facial features in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental delay, hypotonia, and impaired language Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay, hypotonia, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Global developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiac anomalies - developmental delay - facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiac anomalies - developmental delay - facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe global developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental regression Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental regression phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe achondroplasia-developmental delay-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental malformations-deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental malformations-deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
INTELLECTUAL DEVELOPMENTAL DISOR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the INTELLECTUAL DEVELOPMENTAL DISOR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental delay and seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental delay and seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrocephaly-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrocephaly-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pancytopenia-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancytopenia-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Genetic developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ3-related developmental disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ3-related developmental disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ3-related Autism and developmental disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ3-related Autism and developmental disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Moderate global developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Moderate global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GNAO1-related developmental delay-seizures-movement disorder spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GNAO1-related developmental delay-seizures-movement disorder spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia-severe developmental delay-epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia-severe developmental delay-epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-brachydactyly-obesity-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-brachydactyly-obesity-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Unclassified developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Unclassified developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BSCL2-related Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BSCL2-related Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Noonan Syndrome-like developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan Syndrome-like developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PUM1-associated developmental disability-ataxia-seizure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PUM1-associated developmental disability-ataxia-seizure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder and retinitis pigmentosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder and retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pervasive developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pervasive developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder- Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder- phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HCN2 related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HCN2 related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SNAP25-related early-onset developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SNAP25-related early-onset developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pili torti-developmental delay-neurological abnormalities syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pili torti-developmental delay-neurological abnormalities syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SEPHS1-related developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SEPHS1-related developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pubertal developmental failure in females Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pubertal developmental failure in females phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GRIN2B-related developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GRIN2B-related developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
USP9X-related intellectual developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the USP9X-related intellectual developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FRYL-related developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FRYL-related developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNA3-associated developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNA3-associated developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GABRA4-related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GABRA4-related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental language disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental language disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Developmental language disorder (linguistic errors) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental language disorder (linguistic errors) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Developmental language disorder (syntactic complexity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental language disorder (syntactic complexity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Frontometaphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontometaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Czech dysplasia metatarsal type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Czech dysplasia metatarsal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloperipheral dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloperipheral dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wolcott-Rallison dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wolcott-Rallison dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniodiaphyseal dysplasia, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypohidrotic X-linked ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypohidrotic X-linked ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteoglophonic dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteoglophonic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gracile bone dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gracile bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontonasal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontonasal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylometaphyseal dysplasia, Kozlowski type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaphyseal dysplasia, Kozlowski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Odontoonychodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Odontoonychodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal-hepatic-pancreatic dysplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acampomelic campomelic dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acampomelic campomelic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia/short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia, Missouri type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia, Missouri type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypohidrotic ectodermal dysplasia with immune deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypohidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofrontonasal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofrontonasal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anhidrotic ectodermal dysplasia with immune deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia, kimberley type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia, kimberley type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiac valvular dysplasia, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiac valvular dysplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trichorhinophalangeal dysplasia type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trichorhinophalangeal dysplasia type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diastrophic dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diastrophic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thanatophoric dysplasia type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thanatophoric dysplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diaphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cleidocranial dysplasia, forme fruste, with brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cleidocranial dysplasia, forme fruste, with brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniometaphyseal dysplasia, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniometaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schneckenbecken dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schneckenbecken dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acromicric dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acromicric dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Terminal osseous dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Terminal osseous dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitreoretinopathy with phalangeal epiphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitreoretinopathy with phalangeal epiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acromesomelic dysplasia Maroteaux type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acromesomelic dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rapp-Hodgkin ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rapp-Hodgkin ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schimke immunoosseous dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schimke immunoosseous dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acrocapitofemoral dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acrocapitofemoral dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hay-Wells syndrome of ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hay-Wells syndrome of ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculodentodigital dysplasia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculodentodigital dysplasia, autosomal recessive 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.
Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Greenberg dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Greenberg dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Boomerang dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Boomerang dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniolenticulosutural dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniolenticulosutural dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculodentodigital dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculodentodigital dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Desbuquois dysplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Desbuquois dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia, complex, with other brain malformations 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia, complex, with other brain malformations 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia, complex, with other brain malformations 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia, complex, with other brain malformations 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia, complex, with other brain malformations 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bent bone dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bent bone dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chondroectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chondroectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ischiopatellar dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ischiopatellar dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Geleophysic dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Geleophysic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Geleophysic dysplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Geleophysic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia, Aggrecan type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia, Aggrecan type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alveolar capillary dysplasia with misalignment of pulmonary veins Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brachyrachia (short spine dysplasia) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia-focal epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia Strudwick type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia Strudwick type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Septo-optic dysplasia sequence Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia Maroteaux type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylo-megaepiphyseal-metaphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylo-megaepiphyseal-metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cranioectodermal dysplasia 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cranioectodermal dysplasia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cranioectodermal dysplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cranioectodermal dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cranioectodermal dysplasia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cranioectodermal dysplasia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cranioectodermal dysplasia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cranioectodermal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrous dysplasia of jaw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrous dysplasia of jaw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Smith McCort dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Smith McCort dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia congenita Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia skin fragility syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia, pakistani type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia, pakistani type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kniest dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kniest dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Otospondylomegaepiphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Otospondylomegaepiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylometaepiphyseal dysplasia short limb-hand type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia-syndactyly syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia-syndactyly syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Metatrophic dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Metatrophic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontonasal dysplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontonasal dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontonasal dysplasia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontonasal dysplasia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hidrotic ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyssegmental dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dyssegmental dysplasia from the curated CTD Gene-Disease Associations dataset.
Frontometaphyseal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Frontometaphyseal dysplasia from the curated CTD Gene-Disease Associations dataset.
GNATHODIAPHYSEAL DYSPLASIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GNATHODIAPHYSEAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia 3, Anhidrotic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia 3, Anhidrotic from the curated CTD Gene-Disease Associations dataset.
Acrocapitofemoral Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acrocapitofemoral Dysplasia from the curated CTD Gene-Disease Associations dataset.
Thanatophoric dysplasia, type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thanatophoric dysplasia, type 2 from the curated CTD Gene-Disease Associations dataset.
Cardiac valvular dysplasia, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac valvular dysplasia, X-linked from the curated CTD Gene-Disease Associations dataset.
GREENBERG DYSPLASIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GREENBERG DYSPLASIA from the curated CTD Gene-Disease Associations dataset.
Craniolenticulosutural Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniolenticulosutural Dysplasia from the curated CTD Gene-Disease Associations dataset.
Mandibuloacral dysplasia with type B lipodystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mandibuloacral dysplasia with type B lipodystrophy from the curated CTD Gene-Disease Associations dataset.
CRANIOECTODERMAL DYSPLASIA 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CRANIOECTODERMAL DYSPLASIA 2 from the curated CTD Gene-Disease Associations dataset.
ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 from the curated CTD Gene-Disease Associations dataset.
Focal cortical dysplasia of Taylor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Focal cortical dysplasia of Taylor from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.
Multicystic renal dysplasia, bilateral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multicystic renal dysplasia, bilateral from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Cranioectodermal Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cranioectodermal Dysplasia from the curated CTD Gene-Disease Associations dataset.
TERMINAL OSSEOUS DYSPLASIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TERMINAL OSSEOUS DYSPLASIA from the curated CTD Gene-Disease Associations dataset.
Thanatophoric Dysplasia, Type I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thanatophoric Dysplasia, Type I from the curated CTD Gene-Disease Associations dataset.
Acromicric dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromicric dysplasia from the curated CTD Gene-Disease Associations dataset.
Langer mesomelic dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Langer mesomelic dysplasia from the curated CTD Gene-Disease Associations dataset.
Cleidocranial Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.
FRONTONASAL DYSPLASIA 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FRONTONASAL DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.
FRONTONASAL DYSPLASIA 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FRONTONASAL DYSPLASIA 2 from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Bronchopulmonary Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchopulmonary Dysplasia from the curated CTD Gene-Disease Associations dataset.
Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondylo-Megaepiphyseal-Metaphyseal Dysplasia from the curated CTD Gene-Disease Associations dataset.
Spondyloepiphyseal Dysplasia Tarda, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepiphyseal Dysplasia Tarda, X-Linked from the curated CTD Gene-Disease Associations dataset.
Polyostotic osteolytic dysplasia, hereditary expansile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyostotic osteolytic dysplasia, hereditary expansile from the curated CTD Gene-Disease Associations dataset.
FRONTONASAL DYSPLASIA 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FRONTONASAL DYSPLASIA 3 from the curated CTD Gene-Disease Associations dataset.
Schimke immunoosseous dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schimke immunoosseous dysplasia from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia from the curated CTD Gene-Disease Associations dataset.
ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.
Craniofrontonasal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniofrontonasal dysplasia from the curated CTD Gene-Disease Associations dataset.
Oculodentodigital Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculodentodigital Dysplasia from the curated CTD Gene-Disease Associations dataset.
Anal sphincter dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anal sphincter dysplasia from the curated CTD Gene-Disease Associations dataset.
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platyspondylic Lethal Skeletal Dysplasia, Torrance Type from the curated CTD Gene-Disease Associations dataset.
Anauxetic dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anauxetic dysplasia from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.
Hypopituitarism and septooptic 'dysplasia' Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.
Odontoonychodermal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Odontoonychodermal dysplasia from the curated CTD Gene-Disease Associations dataset.
Spondylometaphyseal dysplasia, Kozlowski type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondylometaphyseal dysplasia, Kozlowski type from the curated CTD Gene-Disease Associations dataset.
Cortical Dysplasia-Focal Epilepsy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
SPONDYLOPERIPHERAL DYSPLASIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPONDYLOPERIPHERAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.
Spondyloepiphyseal Dysplasia, Kimberley Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepiphyseal Dysplasia, Kimberley Type from the curated CTD Gene-Disease Associations dataset.
Craniometaphyseal Dysplasia, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniometaphyseal Dysplasia, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Schneckenbecken dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schneckenbecken dysplasia from the curated CTD Gene-Disease Associations dataset.
Thanatophoric Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thanatophoric Dysplasia from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia/ skin fragility syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Ghosal Hematodiaphyseal Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ghosal Hematodiaphyseal Dysplasia from the curated CTD Gene-Disease Associations dataset.
Smith-McCort Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Smith-McCort Dysplasia from the curated CTD Gene-Disease Associations dataset.
Diastrophic dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diastrophic dysplasia from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Fibrous Dysplasia, Polyostotic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrous Dysplasia, Polyostotic from the curated CTD Gene-Disease Associations dataset.
RETINAL DYSPLASIA, PRIMARY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset.
SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE from the curated CTD Gene-Disease Associations dataset.
Fibrous Dysplasia of Bone Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrous Dysplasia of Bone from the curated CTD Gene-Disease Associations dataset.
Metaphyseal Dysplasia without Hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.
OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.
Boomerang dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Boomerang dysplasia from the curated CTD Gene-Disease Associations dataset.
Pelviscapular dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pelviscapular dysplasia from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.
GELEOPHYSIC DYSPLASIA 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GELEOPHYSIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.
Torticollis keloids cryptorchidism renal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Torticollis keloids cryptorchidism renal dysplasia from the curated CTD Gene-Disease Associations dataset.
Campomelic Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Campomelic Dysplasia from the curated CTD Gene-Disease Associations dataset.
Alveolar capillary dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alveolar capillary dysplasia from the curated CTD Gene-Disease Associations dataset.
Ischiopatellar dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ischiopatellar dysplasia from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy 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.
ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
DENTIN DYSPLASIA, TYPE II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DENTIN DYSPLASIA, TYPE II from the curated CTD Gene-Disease Associations dataset.
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.
Mandibuloacral dysplasia with type A lipodystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mandibuloacral dysplasia with type A lipodystrophy from the curated CTD Gene-Disease Associations dataset.
Oculodentodigital Dysplasia, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculodentodigital Dysplasia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Spondyloepimetaphyseal Dysplasia, Missouri Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Missouri Type 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.
Acromesomelic dysplasia, Maroteaux type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromesomelic dysplasia, Maroteaux type from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia 1, Anhidrotic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia 1, Anhidrotic from the curated CTD Gene-Disease Associations dataset.
ACROPECTOROVERTEBRAL DYSPLASIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ACROPECTOROVERTEBRAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.
Spondyloepiphyseal dysplasia, congenita Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepiphyseal dysplasia, congenita from the curated CTD Gene-Disease Associations dataset.
Spondyloepimetaphyseal Dysplasia, Pakistani Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Pakistani Type from the curated CTD Gene-Disease Associations dataset.
Spondyloepimetaphyseal Dysplasia, Aggrecan Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Aggrecan Type from the curated CTD Gene-Disease Associations dataset.
Parietal Foramina With Cleidocranial Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parietal Foramina With Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.
Eiken Skeletal Dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eiken Skeletal Dysplasia from the curated CTD Gene-Disease Associations dataset.
Kniest dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Kniest dysplasia from the curated CTD Gene-Disease Associations dataset.
SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.
Frontonasal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Frontonasal dysplasia from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia, hypohidrotic, with immune deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, hypohidrotic, with immune deficiency from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.
craniometaphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease craniometaphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spondyloepimetaphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spondyloepimetaphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
thanatophoric dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease thanatophoric dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
campomelic dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease campomelic dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
otospondylomegaepiphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease otospondylomegaepiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
kniest dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease kniest dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sost-related sclerosing bone dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
boomerang dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease boomerang dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cleidocranial dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cleidocranial dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spondyloepiphyseal dysplasia congenita Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spondyloepiphyseal dysplasia congenita from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spondyloepimetaphyseal dysplasia, strudwick type Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spondyloepimetaphyseal dysplasia, strudwick type from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
diastrophic dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease diastrophic dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
hypohidrotic ectodermal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hypohidrotic ectodermal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple epiphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
thanatophoric dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thanatophoric dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
metaphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease metaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spondyloepimetaphyseal dysplasia, strudwick type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spondyloepimetaphyseal dysplasia, strudwick type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dentin dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentin dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spondyloepimetaphyseal dysplasia, missouri type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spondyloepimetaphyseal dysplasia, missouri type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spondyloepiphyseal dysplasia congenita Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spondyloepiphyseal dysplasia congenita in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spondyloepimetaphyseal dysplasia, sponastrime type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spondyloepimetaphyseal dysplasia, sponastrime type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple epiphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acromesomelic dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acromesomelic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anauxetic dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anauxetic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
craniometaphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease craniometaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sost-related sclerosing bone dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cleidocranial dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cleidocranial dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mammary dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mammary dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acromesomelic dysplasia, maroteaux type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acromesomelic dysplasia, maroteaux type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schneckenbecken dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schneckenbecken dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
otospondylomegaepiphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease otospondylomegaepiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
craniodiaphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease craniodiaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diastrophic dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diastrophic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
thymic dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thymic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypohidrotic ectodermal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypohidrotic ectodermal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
campomelic dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease campomelic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spondyloepimetaphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spondyloepimetaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
kniest dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease kniest dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
boomerang dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease boomerang dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acrocapitofemoral dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acrocapitofemoral dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fibrous dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fibrous dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
achondroplasia; musculoskeletal abnormalities; osteochondrodysplasias; thanatophoric dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease achondroplasia; musculoskeletal abnormalities; osteochondrodysplasias; thanatophoric dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple epiphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; infant, newborn, diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibromuscular dysplasia; hypertension; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thanatophoric dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease thanatophoric dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intestinal neuronal dysplasia type b (ind b) Gene Set From GAD Gene-Disease Associations genes associated with the disease intestinal neuronal dysplasia type b (ind b) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; heart failure Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm Gene Set From GAD Gene-Disease Associations genes associated with the disease ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; cardiomyopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; syncope Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; syncope 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.
bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma 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.
pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia 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.
strudwick variant of spondyloepimetaphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease strudwick variant of spondyloepimetaphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple oesophageal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
risk of cervical dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease risk of cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hpv-associated cervical dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease hpv-associated cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; chorioamnionitis Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; chorioamnionitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleidocranial dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleidocranial dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia. Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; ectodermal dysplasia; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; ectodermal dysplasia; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibrous dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease fibrous dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dysplasia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dysplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Bronchopulmonary dysplasia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bronchopulmonary dysplasia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
nail dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the nail dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple epiphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the multiple epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acetabular dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the acetabular dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skeletal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the skeletal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
metaphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the metaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fibrous dysplasia of the bones Gene Set From HPO Gene-Disease Associations genes associated with the fibrous dysplasia of the bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontoparietal cortical dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the frontoparietal cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lethal skeletal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the lethal skeletal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cortical dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
brainstem dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the brainstem dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spondylometaphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the spondylometaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polyostotic fibrous dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the polyostotic fibrous dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystic renal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the cystic renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fingernail dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the fingernail dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
epiphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ectodermal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the spondyloepiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic nerve dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the optic nerve dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multicystic kidney dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the multicystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypohidrotic ectodermal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the hypohidrotic ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polycystic kidney dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the polycystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hair-nail ectodermal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the hair-nail ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
toenail dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the toenail dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diaphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the diaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
septo-optic dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the septo-optic dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysplasia of the femoral head Gene Set From HPO Gene-Disease Associations genes associated with the dysplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Septo-Optic Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Septo-Optic Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bronchopulmonary Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bronchopulmonary Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ectodermal Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ectodermal Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Thanatophoric Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Thanatophoric Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fibromuscular Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fibromuscular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fibrous Dysplasia, Polyostotic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fibrous Dysplasia, Polyostotic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fibrous Dysplasia of Bone Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fibrous Dysplasia of Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cleidocranial Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cleidocranial Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Uterine Cervical Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Uterine Cervical Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Arrhythmogenic Right Ventricular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Adrenocortical dysplasia protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adrenocortical dysplasia protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
?corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the ?corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
?epiphyseal dysplasia, multiple, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloperipheral dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloperipheral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
acampomelic campomelic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the acampomelic campomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
frontometaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the frontometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
campomelic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the campomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
metaphyseal dysplasia without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 4 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
smith-mccort dysplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the smith-mccort dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
parietal foramina with cleidocranial dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the parietal foramina with cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
craniometaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the craniometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
renal-hepatic-pancreatic dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the renal-hepatic-pancreatic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 6, hair/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 6, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia/short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
craniofacial-skeletal-dermatologic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the craniofacial-skeletal-dermatologic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
focal cortical dysplasia, taylor balloon cell type Gene Set From OMIM Gene-Disease Associations genes associated with the focal cortical dysplasia, taylor balloon cell type phenotype from the curated OMIM Gene-Disease Associations dataset.
thanatophoric dysplasia, type i Gene Set From OMIM Gene-Disease Associations genes associated with the thanatophoric dysplasia, type i phenotype from the curated OMIM Gene-Disease Associations dataset.
mandibuloacral dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mandibuloacral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
diastrophic dysplasia, broad bone-platyspondylic variant Gene Set From OMIM Gene-Disease Associations genes associated with the diastrophic dysplasia, broad bone-platyspondylic variant phenotype from the curated OMIM Gene-Disease Associations dataset.
cleft lip/palate-ectodermal dysplasia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cleft lip/palate-ectodermal dysplasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
otospondylomegaepiphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the otospondylomegaepiphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
boomerang dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the boomerang dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
frontonasal dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the frontonasal dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
frontonasal dysplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the frontonasal dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
craniolenticulosutural dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the craniolenticulosutural dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cranioectodermal dysplasia 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cranioectodermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cranioectodermal dysplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cranioectodermal dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cranioectodermal dysplasia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cranioectodermal dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cranioectodermal dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cranioectodermal dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 3, witkop type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 3, witkop type phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylometaepiphyseal dysplasia, short limb-hand type Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 7, hair/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 7, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
oculodentodigital dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the oculodentodigital dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
greenberg skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the greenberg skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
acromesomelic dysplasia, maroteaux type Gene Set From OMIM Gene-Disease Associations genes associated with the acromesomelic dysplasia, maroteaux type phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 5, hair/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 5, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
smith-mccort dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the smith-mccort dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
craniodiaphyseal dysplasia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
septooptic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the septooptic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
acromesomelic dysplasia, hunter-thompson type Gene Set From OMIM Gene-Disease Associations genes associated with the acromesomelic dysplasia, hunter-thompson type phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia, missouri type Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia, missouri type phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 11 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set From OMIM Gene-Disease Associations genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tarda Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepiphyseal dysplasia tarda phenotype from the curated OMIM Gene-Disease Associations dataset.
autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 1, hypohidrotic, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 1, hypohidrotic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
diastrophic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the diastrophic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
platyspondylic skeletal dysplasia, torrance type Gene Set From OMIM Gene-Disease Associations genes associated with the platyspondylic skeletal dysplasia, torrance type phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia-syndactyly syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia-syndactyly syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
schneckenbecken dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the schneckenbecken dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
dentin dysplasia, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the dentin dysplasia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
de la chapelle dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the de la chapelle dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical dysplasia-focal epilepsy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cortical dysplasia-focal epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
craniometaphyseal dysplasia, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the craniometaphyseal dysplasia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 4, hair/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 4, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
alveolar capillary dysplasia with misalignment of pulmonary veins Gene Set From OMIM Gene-Disease Associations genes associated with the alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated OMIM Gene-Disease Associations dataset.
kniest dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the kniest dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
otodental dysplasia chromsome deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the otodental dysplasia chromsome deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopia and deafness Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
acrocapitofemoral dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the acrocapitofemoral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tarda with progressive arthropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepiphyseal dysplasia tarda with progressive arthropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniofrontonasal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the craniofrontonasal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
{renal dysplasia, cystic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {renal dysplasia, cystic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
langer mesomelic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the langer mesomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
vitreoretinopathy with phalangeal epiphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the vitreoretinopathy with phalangeal epiphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
bent bone dysplasia syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the bent bone dysplasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
acromicric dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the acromicric dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
acropectorovertebral dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the acropectorovertebral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
dentin dysplasia, type i, with microdontia and misshapen teeth Gene Set From OMIM Gene-Disease Associations genes associated with the dentin dysplasia, type i, with microdontia and misshapen teeth phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylometaphyseal dysplasia, kozlowski type Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaphyseal dysplasia, kozlowski type phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 10 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 12 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, sensorineural deafness, and renal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, sensorineural deafness, and renal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation-skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation-skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
desbuquois dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the desbuquois dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylo-megaepiphyseal-metaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the spondylo-megaepiphyseal-metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
anauxetic dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the anauxetic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 9, hair/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 9, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
cleidocranial dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia/skin fragility syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia/skin fragility syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
gnathodiaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the gnathodiaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
focal facial dermal dysplasia 4 Gene Set From OMIM Gene-Disease Associations genes associated with the focal facial dermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia with joint laxity, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 8, hair/tooth/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 8, hair/tooth/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
schimke immunoosseous dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the schimke immunoosseous dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia, hypohidrotic, with immune deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia, hypohidrotic, with immune deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia-syndactyly syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia-syndactyly syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
mandibuloacral dysplasia with type b lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the mandibuloacral dysplasia with type b lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
terminal osseous dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the terminal osseous dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
desbuquois dysplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the desbuquois dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?frontonasal dysplasia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?frontonasal dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiac valvular dysplasia, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the cardiac valvular dysplasia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
campomelic dysplasia with autosomal sex reversal Gene Set From OMIM Gene-Disease Associations genes associated with the campomelic dysplasia with autosomal sex reversal phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 5 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 4 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 6 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 9 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 8 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
geleophysic dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the geleophysic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
geleophysic dysplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the geleophysic dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
dyssegmental dysplasia, silverman-handmaker type Gene Set From OMIM Gene-Disease Associations genes associated with the dyssegmental dysplasia, silverman-handmaker type phenotype from the curated OMIM Gene-Disease Associations dataset.
gracile bone dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the gracile bone dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 2 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
odontoonychodermal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the odontoonychodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
cleidocranial dysplasia, forme fruste, with brachydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the cleidocranial dysplasia, forme fruste, with brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical dysplasia, complex, with other brain malformations 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical dysplasia, complex, with other brain malformations 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical dysplasia, complex, with other brain malformations 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical dysplasia, complex, with other brain malformations 6 Gene Set From OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

Harmonizome 3.0

developmental dysplasia of the hip 2 Gene Set

Developmental dysplasia of the hip 2 Gene Set

DEVELOPMENTAL DYSPLASIA OF THE HIP 1 Gene Set

Developmental Dysplasia Of The Hip 1 Gene Set

Developmental dysplasia of the hip Gene Set

Developmental dysplasia of the hip 1 Gene Set

Developmental dysplasia of the hip Gene Set

Developmental dysplasia of the hip Gene Set

degenerative arthropathy ; hip fractures; osteoarthritis; osteoarthritis, hip; osteoarthritis, knee; osteoporosis Gene Set

hip fractures; osteoarthritis, hip Gene Set

bone diseases, developmental; osteoarthritis, hip Gene Set

Hip Dysplasia, Beukes Type Gene Set

osteoarthritis; hip dysplasia Gene Set

hip dysplasia Gene Set

hip dysplasia, beukes type Gene Set

Congenital Dysplasia Of The Hip Gene Set

Hip Dysplasia Gene Set

Namaqualand Hip Dysplasia Gene Set

Hip Dysplasia, Beukes Type Gene Set

Hip Dysplasia, Congenital, Nonsyndromic Gene Set

Beukes hip dysplasia Gene Set

Namaqualand hip dysplasia Gene Set

Hip dysplasia Gene Set

Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis Gene Set

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms Gene Set

Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set

Osteoarthritis, Hip Gene Set

Hip Fractures Gene Set

Hip Gene Set

Waist-Hip Ratio Gene Set

osteoarthritis, hip; osteoarthritis, knee Gene Set

waist-hip ratio Gene Set

hip bone loss and fracture Gene Set

hip fractures; osteoporosis Gene Set

hip dislocation, congenital; joint instability Gene Set

fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set

osteoarthritis, hip Gene Set

osteoarthritis; osteoarthritis, hip; osteoarthritis, knee Gene Set

fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene Set

hip fractures Gene Set

hip geometry Gene Set

hip dislocation, congenital Gene Set

hip fractures; osteoporosis, postmenopausal Gene Set

arthralgia; osteoarthritis, hip Gene Set

fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set

bone mineral density (hip) Gene Set

hip Gene Set

hip bone size Gene Set

breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set

hip Gene Set

Hip bone size Gene Set

Bone mineral density (hip) Gene Set

Waist-hip ratio Gene Set

Osteoarthritis (hip) Gene Set

Waist-to-hip circumference ratio (interaction) Gene Set

Hip geometry Gene Set

hip osteoarthritis Gene Set

abnormality of the hip bone Gene Set

abnormality of the hip joint Gene Set

congenital bilateral hip dislocation Gene Set

hip osteoarthritis Gene Set

limited hip movement Gene Set

abnormality of the hip bone Gene Set

hip contracture Gene Set

abnormality of the hip-girdle musculature Gene Set

limited hip extension Gene Set

arthralgia of the hip Gene Set

decreased hip abduction Gene Set

congenital hip dislocation Gene Set

hip dislocation Gene Set

Osteoarthritis, Hip Gene Set

Hip Dislocation Gene Set

Hip Fractures Gene Set

Hip Dislocation, Congenital Gene Set

hip Gene Set

hip joint Gene Set

Hip Pain Chronic Gene Set

Hip Contracture Gene Set