Name

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

sost Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term sost in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

SOST Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for SOST from the Pathway Commons Protein-Protein Interactions dataset.

cocaine-related disorders; opioid-related disorders; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cocaine-related disorders; opioid-related disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

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.

alcohol-related disorders; cocaine-related disorders; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related disorders; cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; opioid-related disorders; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; opioid-related disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anticoagulant complications; bleeding events, warfarin therapy-related; overanticoagulation, warfarin therapy-related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anticoagulant complications; bleeding events, warfarin therapy-related; overanticoagulation, warfarin therapy-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Actin-related protein 8/Plant actin-related protein 9 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 8/Plant actin-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations 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.

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.

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.

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.

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.

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.

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.

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.

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.

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive sclerosing poliodystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.

Cholangitis, Sclerosing Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholangitis, Sclerosing from the curated CTD Gene-Disease Associations dataset.

Cholangitis, Sclerosing Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Cholangitis, Sclerosing in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

sclerosing liposarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sclerosing liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pulmonary sclerosing hemangioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pulmonary sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

subacute sclerosing panencephalitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sclerosing cholangitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sclerosing keratitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sclerosing keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sclerosing hemangioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sclerosing hepatic carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cirrhosis, biliary primary; cholangitis, sclerosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cirrhosis, biliary primary; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ulcerative colitis; cholangitis, sclerosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ulcerative colitis; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; cholangitis, sclerosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary sclerosing cholangitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease primary sclerosing cholangitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

panencephalitis, subacute sclerosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease panencephalitis, subacute sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

subacute sclerosing panencephalitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sclerosing Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term sclerosing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Primary sclerosing cholangitis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Sclerosing cholangitis and ulcerative colitis (combined) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sclerosing cholangitis and ulcerative colitis (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

sclerosing cholangitis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease sclerosing cholangitis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Subacute Sclerosing Panencephalitis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Subacute Sclerosing Panencephalitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cholangitis, Sclerosing Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cholangitis, Sclerosing phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cholangitis, primary sclerosing Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholangitis, primary sclerosing phenotype from the curated OMIM Gene-Disease Associations dataset.

keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratosis linearis with ichthyosis congenita and sclerosing keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis phenotype from the curated OMIM Gene-Disease Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

{bone marrow failure, telomere-related, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bone marrow failure, telomere-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

bone resorption; fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; bone responsiveness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; bone responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low bone-mineral density and rapid postmenopausal bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

regulation of bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 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.

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.

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.

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.

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.

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.

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.

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.

craniometaphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation Evidence Scores

genes involed in the disease kniest dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

boomerang dysplasia Gene Set

From DISEASES Curated Gene-Disease Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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.

cleidocranial dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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.

connective tissue dysplasias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue dysplasias 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.

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.

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.

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.

dysplasiacardiomypath Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiacardiomypath in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dysplasias Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasias in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dysplasiarelated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiarelated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dysplasiadeath Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiadeath in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dysplasiaskin Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiaskin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dysplasiacarcinoma Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiacarcinoma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations 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.

dysplasiainducing Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiainducing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dysplasiacardiomyopathy Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysplasiacardiomyopathy 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

cortical dysplasia, complex, with other brain malformations 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

focal facial dermal dysplasia 3, setleis type Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal facial dermal dysplasia 3, setleis type phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

czech dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the czech dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia, aggrecan type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia, aggrecan type phenotype from the curated OMIM Gene-Disease Associations dataset.

oculodentodigital dysplasia, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculodentodigital dysplasia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mesomelic dysplasia, kantaputra type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mesomelic dysplasia, kantaputra type phenotype from the curated OMIM Gene-Disease Associations dataset.

cleidocranial dysplasia, forme fruste, dental anomalies only Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleidocranial dysplasia, forme fruste, dental anomalies only phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia, kimberley type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia, kimberley type phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

metatropic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the metatropic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

thanatophoric dysplasia, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the thanatophoric dysplasia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

?renal-hepatic-pancreatic dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?renal-hepatic-pancreatic dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteoglophonic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteoglophonic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 2, clouston type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 2, clouston type phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Gene Set

From Reactome Pathways

proteins participating in the Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) pathway from the Reactome Pathways dataset.

Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.

Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) Gene Set

From Reactome Pathways

proteins participating in the Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) pathway from the Reactome Pathways dataset.

chronic ulcerative colitis (CUC), ulcerative colitis?associated dysplasia (UCD), colitis-associated cancer (CAC) Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease chronic ulcerative colitis (CUC), ulcerative colitis?associated dysplasia (UCD), colitis-associated cancer (CAC) from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Superior colliculus, motor related, intermediate white layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, intermediate white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Midbrain, sensory related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Midbrain, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Thalamus, polymodal association cortex related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Thalamus, polymodal association cortex related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, deep white layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, deep white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Midbrain, behavioral state related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Midbrain, behavioral state related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, sensory related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Midbrain, motor related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Midbrain, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, deep gray layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, deep gray layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, intermediate gray layer, sublayer a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, intermediate gray layer, sublayer c Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer c relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, intermediate gray layer, sublayer b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pons, motor related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pons, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Thalamus, sensory-motor cortex related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Thalamus, sensory-motor cortex related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pons, behavioral state related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pons, behavioral state related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, intermediate gray layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, intermediate gray layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pons, sensory related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pons, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medulla, motor related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medulla, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medulla, sensory related Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medulla, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

tnf/stress related signaling Gene Set

From Biocarta Pathways

proteins participating in the tnf/stress related signaling pathway from the Biocarta Pathways dataset.

Myofibrillar myopathy, ZASP-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myofibrillar myopathy, ZASP-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

RRM2B-related mitochondrial disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, histidine-rich glycoprotein-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, histidine-rich glycoprotein-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myofibrillar myopathy, filamin C-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myofibrillar myopathy, filamin C-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FLNB-Related Disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the FLNB-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ZNF711-Related X-linked Mental Retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NSDHL-Related Disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NSDHL-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Age-related macular degeneration 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Age-related macular degeneration 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Age-related macular degeneration 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Age-related macular degeneration 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

WFS1-Related Disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the WFS1-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Age-related macular degeneration 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Age-related macular degeneration 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Age-related macular degeneration 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Age-related macular degeneration 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GATA-1-related thrombocytopenia with dyserythropoiesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GATA-1-related thrombocytopenia with dyserythropoiesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY gonadal dysgenesis, complete, dhh-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY gonadal dysgenesis, complete, dhh-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CATSPER-Related Male Infertility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CATSPER-Related Male Infertility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MYH9 related disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MYH9 related disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOC-3 (biogenesis of lysosome-related organelles complex 3) Gene Set

From CORUM Protein Complexes

proteins in the BLOC-3 (biogenesis of lysosome-related organelles complex 3) protein complex from the CORUM Protein Complexes dataset.

BLOC-1 (biogenesis of lysosome-related organelles complex 1) Gene Set

From CORUM Protein Complexes

proteins in the BLOC-1 (biogenesis of lysosome-related organelles complex 1) protein complex from the CORUM Protein Complexes dataset.

BLOC-2 (biogenesis of lysosome-related organelles complex 2) Gene Set

From CORUM Protein Complexes

proteins in the BLOC-2 (biogenesis of lysosome-related organelles complex 2) protein complex from the CORUM Protein Complexes dataset.

SWI-SNF chromatin remodeling-related-BRCA1 complex Gene Set

From CORUM Protein Complexes

proteins in the SWI-SNF chromatin remodeling-related-BRCA1 complex protein complex from the CORUM Protein Complexes dataset.

SWI/SNF-related complex Gene Set

From CORUM Protein Complexes

proteins in the SWI/SNF-related complex protein complex from the CORUM Protein Complexes dataset.

myristoylated autocamtide-2-related inhibitory peptide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical myristoylated autocamtide-2-related inhibitory peptide from the curated CTD Gene-Chemical Interactions dataset.

calcitonin gene-related peptide (8-37) Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical calcitonin gene-related peptide (8-37) from the curated CTD Gene-Chemical Interactions dataset.

Macular Degeneration, Age-Related, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 11 from the curated CTD Gene-Disease Associations dataset.

AIDS-Related Opportunistic Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AIDS-Related Opportunistic Infections from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 10 from the curated CTD Gene-Disease Associations dataset.

Opioid-Related Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Opioid-Related Disorders from the curated CTD Gene-Disease Associations dataset.

Glaucoma-Related Pigment Dispersion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma-Related Pigment Dispersion Syndrome from the curated CTD Gene-Disease Associations dataset.

Drug Metabolism, Poor, CYP2D6-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug Metabolism, Poor, CYP2D6-Related from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Drug Metabolism, Poor, CYP2C19-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug Metabolism, Poor, CYP2C19-Related from the curated CTD Gene-Disease Associations dataset.

AIDS-Related Complex Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AIDS-Related Complex from the curated CTD Gene-Disease Associations dataset.

Alcohol-Related Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alcohol-Related Disorders from the curated CTD Gene-Disease Associations dataset.

NEVER IN MITOSIS GENE A-RELATED KINASE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEVER IN MITOSIS GENE A-RELATED KINASE 1 from the curated CTD Gene-Disease Associations dataset.

Cerebral Amyloid Angiopathy, App-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, App-Related from the curated CTD Gene-Disease Associations dataset.

NOG-Related-Symphalangism Spectrum Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOG-Related-Symphalangism Spectrum Disorder from the curated CTD Gene-Disease Associations dataset.

CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 from the curated CTD Gene-Disease Associations dataset.

Amyloidosis, Hereditary, Transthyretin-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyloidosis, Hereditary, Transthyretin-Related from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 9 from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 3 from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 2 from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 1 from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 7 from the curated CTD Gene-Disease Associations dataset.

FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset.

Lymphoma, AIDS-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lymphoma, AIDS-Related from the curated CTD Gene-Disease Associations dataset.

AIDS-related Kaposi sarcoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AIDS-related Kaposi sarcoma from the curated CTD Gene-Disease Associations dataset.

Cocaine-Related Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cocaine-Related Disorders from the curated CTD Gene-Disease Associations dataset.

Substance-Related Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Substance-Related Disorders from the curated CTD Gene-Disease Associations dataset.

46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related from the curated CTD Gene-Disease Associations dataset.

Cataract, Age-Related Cortical, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Age-Related Cortical, 1 from the curated CTD Gene-Disease Associations dataset.

SCAPULOPERONEAL MYOPATHY, MYH7-RELATED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCAPULOPERONEAL MYOPATHY, MYH7-RELATED from the curated CTD Gene-Disease Associations dataset.

Macular Degeneration, Age-Related, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Degeneration, Age-Related, 4 from the curated CTD Gene-Disease Associations dataset.

Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related from the curated CTD Gene-Disease Associations dataset.

Gout, HPRT-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gout, HPRT-Related from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

Age-Related Hearing Impairment 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Age-Related Hearing Impairment 1 from the curated CTD Gene-Disease Associations dataset.

Cardiac Arrhythmia, Ankyrin-B-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Arrhythmia, Ankyrin-B-Related from the curated CTD Gene-Disease Associations dataset.

MYH9-Related Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYH9-Related Disorders from the curated CTD Gene-Disease Associations dataset.

Amphetamine-Related Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amphetamine-Related Disorders from the curated CTD Gene-Disease Associations dataset.

Myostatin-related muscle hypertrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myostatin-related muscle hypertrophy from the curated CTD Gene-Disease Associations dataset.

Drug-Related Side Effects and Adverse Reactions Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug-Related Side Effects and Adverse Reactions from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Lmna-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.

Substance-Related Disorders Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Substance-Related Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

age related macular degeneration Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease age related macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

substance-related disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease substance-related disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

alcohol-related birth defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

substance-related disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease substance-related disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

age related macular degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

alcohol-related neurodevelopmental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebral amyloid angiopathy-related hemorrhage. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy-related hemorrhage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids dementia complex; aids related dementia complex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids dementia complex; aids related dementia complex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-related disorders; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related disorders; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

speech disorders; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease speech disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apnea; opioid-related disorders; pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apnea; opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

5-fluorouracil- related toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease 5-fluorouracil- related toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

methadone-related deaths Gene Set

From GAD Gene-Disease Associations

genes associated with the disease methadone-related deaths in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; herpes genitalis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; herpes genitalis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microangiopathy- related cerebral damage (marcd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microangiopathy- related cerebral damage (marcd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, malaria related; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cocaine-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cocaine-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

event-related prefrontal activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease event-related prefrontal activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ill health, sheep dip related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ill health, sheep dip related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angiotensin-converting enzyme inhibitor-related cough Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angiotensin-converting enzyme inhibitor-related cough in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-related macular degeneration (wet) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-related macular degeneration (wet) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

p300 event-related potential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease p300 event-related potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psychoses, substance-induced; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psychoses, substance-induced; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; prenatal exposure delayed effects; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mouth neoplasms; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mouth neoplasms; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cigarette smoking- related bladder cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cigarette smoking- related bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; tuberculosis; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; tuberculosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; cocaine-related disorders; substance withdrawal syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; cocaine-related disorders; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cough, angiotensin-converting enzyme; inhibitor-related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cough, angiotensin-converting enzyme; inhibitor-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amphetamine-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

opioid-related disorders; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease opioid-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amphetamine-related disorders; brain diseases, metabolic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; brain diseases, metabolic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-related skeletal disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-related skeletal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

opioid-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease opioid-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

liver steatosis, hepatitis c virus-related; steatohepatitis, nonalcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver steatosis, hepatitis c virus-related; steatohepatitis, nonalcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cocaine-related disorders; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular degeneration, age-related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration, age-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis b-related hepatocellular carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b-related hepatocellular carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heroin dependence; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heroin dependence; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial age-related macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amphetamine-related disorders; psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuroblastoma; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuroblastoma; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

opioid-related disorders; substance withdrawal syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease opioid-related disorders; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

emphysema; pulmonary disease, chronic obstructive; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease emphysema; pulmonary disease, chronic obstructive; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ovarian cancer- methotrexate related toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ovarian cancer- methotrexate related toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes related glucose homeostasis trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes related glucose homeostasis trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-related genes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-related genes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amphetamine-related disorders; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; marijuana abuse; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; marijuana abuse; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuropathy, alzheimer's disease related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuropathy, alzheimer's disease related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

waist circumference and related phenotypes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease waist circumference and related phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy-related first time venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy-related first time venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-related maculopathy. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-related maculopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting insulin-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting insulin-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amphetamine-related disorders; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; drug hypersensitivity; pneumonia, pneumocystis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; drug hypersensitivity; pneumonia, pneumocystis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes; serum triacylglycerol ; ogtt-related insulinaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes; serum triacylglycerol ; ogtt-related insulinaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes related glucose homeostasis traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes related glucose homeostasis traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-related polyneuropathy; alcoholic neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related polyneuropathy; alcoholic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety-related temperament and behavior problems Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety-related temperament and behavior problems in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aflatoxin-related hepatocarcinogenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aflatoxin-related hepatocarcinogenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes related insulin traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes related insulin traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; substance-related disorders; viremia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c, chronic; substance-related disorders; viremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anger-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anger-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-related maculopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-related maculopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mesothelin-related protein levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mesothelin-related protein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hematopoietic outcomes, lead exposure related; lead Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hematopoietic outcomes, lead exposure related; lead in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety-related personality traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety-related personality traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-related macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prevalent type 2 diabetes and related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prevalent type 2 diabetes and related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-related disorders; alcoholism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related disorders; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sepsis-related organ dysfunction and shock after burn injury Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sepsis-related organ dysfunction and shock after burn injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

agricultural workers' diseases; dna damage; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease agricultural workers' diseases; dna damage; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

substance withdrawal syndrome; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease substance withdrawal syndrome; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

allergic diseases (bronchial asthma. atopic dermatitis and/or food-related anaphylaxis) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease allergic diseases (bronchial asthma. atopic dermatitis and/or food-related anaphylaxis) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; dermatitis and eczema; anaphylaxis, food-related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; dermatitis and eczema; anaphylaxis, food-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; cocaine-related disorders; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; cocaine-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acei-related cough Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acei-related cough in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; cocaine-related disorders; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting glucose-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting glucose-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

opioid-related disorders; pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; hiv infections; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; hiv infections; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis-related phenotypes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis-related phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

treatment-related leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease treatment-related leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

li-fraumeni and related syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease li-fraumeni and related syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

related Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term related in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

response to defense-related nitric oxide production by other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the response to defense-related nitric oxide production by other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

response to defense-related host reactive oxygen species production Gene Set

From GO Biological Process Annotations

genes participating in the response to defense-related host reactive oxygen species production biological process from the curated GO Biological Process Annotations dataset.

positive regulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

response to defense-related host nitric oxide production Gene Set

From GO Biological Process Annotations

genes participating in the response to defense-related host nitric oxide production biological process from the curated GO Biological Process Annotations dataset.

modulation by symbiont of defense-related host nitric oxide production Gene Set

From GO Biological Process Annotations

genes participating in the modulation by symbiont of defense-related host nitric oxide production biological process from the curated GO Biological Process Annotations dataset.

induction by symbiont of defense-related host nitric oxide production Gene Set

From GO Biological Process Annotations

genes participating in the induction by symbiont of defense-related host nitric oxide production biological process from the curated GO Biological Process Annotations dataset.

response to defense-related reactive oxygen species production by other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the response to defense-related reactive oxygen species production by other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

induction by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the induction by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

modulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the modulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

positive regulation by symbiont of defense-related host nitric oxide production Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by symbiont of defense-related host nitric oxide production biological process from the curated GO Biological Process Annotations dataset.

oxidoreductase activity, acting on diphenols and related substances as donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors molecular function from the curated GO Molecular Function Annotations dataset.

hydroxymethyl-, formyl- and related transferase activity Gene Set

From GO Molecular Function Annotations

genes performing the hydroxymethyl-, formyl- and related transferase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on diphenols and related substances as donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

calcitonin gene-related peptide receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the calcitonin gene-related peptide receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

ligase activity, forming aminoacyl-trna and related compounds Gene Set

From GO Molecular Function Annotations

genes performing the ligase activity, forming aminoacyl-trna and related compounds molecular function from the curated GO Molecular Function Annotations dataset.

Age-related macular degeneration (CNV vs. GA) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related macular degeneration (GA) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related macular degeneration (GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related macular degeneration (CNV) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related macular degeneration (CNV) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related macular degeneration (wet) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting insulin-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting insulin-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Periodontal disease-related phenotypes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Periodontal disease-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Renal function-related traits (urea) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Renal function-related traits (urea) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Job-related exhaustion Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Job-related exhaustion phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Insulin-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Insulin-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cognitive decline (age-related) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cognitive decline (age-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Sleep-related phenotypes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sleep-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-substance related behavioral disinhibition Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-substance related behavioral disinhibition phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related nuclear cataracts Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related nuclear cataracts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Renal function-related traits (eGRFcrea) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Renal function-related traits (eGRFcrea) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Sexual dysfunction (SSRI/SNRI-related) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related hearing impairment (interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related hearing impairment (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Emphysema-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Emphysema-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related hearing impairment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related hearing impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Osteoporosis-related phenotypes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Osteoporosis-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Diabetes related insulin traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Diabetes related insulin traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Event-related brain oscillations Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Event-related brain oscillations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Waist circumference and related phenotypes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Waist circumference and related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting glucose-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting glucose-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related macular degeneration (extreme sampling) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Lumiracoxib-related liver injury Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Lumiracoxib-related liver injury phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Renal function-related traits (sCR) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Renal function-related traits (sCR) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting glucose-related traits (interaction with BMI) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting glucose-related traits (interaction with BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Dialysis-related mortality Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Dialysis-related mortality phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Renal function-related traits (BUN) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Renal function-related traits (BUN) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hepatocellular carcinoma (hepatitis B virus related) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hepatocellular carcinoma (hepatitis B virus related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related macular degeneration Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting insulin-related traits (interaction with BMI) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting insulin-related traits (interaction with BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

IFN-related cytopenia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the IFN-related cytopenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Obesity-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Obesity-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Chronic obstructive pulmonary disease-related biomarkers Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Chronic obstructive pulmonary disease-related biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

substance-related disorder Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease substance-related disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

age related macular degeneration Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease age related macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

age-related macular degeneration Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the age-related macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal fear/anxiety-related behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paraganglioma-related cranial nerve palsy Gene Set

From HPO Gene-Disease Associations

genes associated with the paraganglioma-related cranial nerve palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

age-related macular degeneration Gene Set

From HPO Gene-Disease Associations

genes associated with the age-related macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

AIDS-Related Opportunistic Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the AIDS-Related Opportunistic Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Opioid-Related Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Opioid-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Prosthesis-Related Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Prosthesis-Related Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Alcohol-Related Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Alcohol-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lymphoma, AIDS-Related Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, AIDS-Related phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cocaine-Related Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cocaine-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Substance-Related Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Substance-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Amphetamine-Related Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Amphetamine-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

PDCD5-related protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PDCD5-related protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ski-related oncogene Sno Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ski-related oncogene Sno protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cadherin-related family member 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cadherin-related family member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

IGFBP-related, CNN Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the IGFBP-related, CNN protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cadherin-related family member 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cadherin-related family member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G protein-coupled receptor 40-related receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G protein-coupled receptor 40-related receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription elongation factor A, SII-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription elongation factor A, SII-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cysteine-rich secretory protein, allergen V5/Tpx-1-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cysteine-rich secretory protein, allergen V5/Tpx-1-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PEX5-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PEX5-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribonucleotide reductase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonucleotide reductase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phenylacetic acid degradation-related domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phenylacetic acid degradation-related domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-inhibited division protein A-related, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-inhibited division protein A-related, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 2/3 complex subunit 1A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 2/3 complex subunit 1A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 2/3 complex subunit 1B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 2/3 complex subunit 1B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pro-FMRFamide-related neuropeptide FF Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pro-FMRFamide-related neuropeptide FF protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Krueppel-associated box-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Krueppel-associated box-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TspO/MBR-related protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TspO/MBR-related protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Putative E3 ubiquitin-protein ligase, makorin-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Putative E3 ubiquitin-protein ligase, makorin-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Angiopoietin-related protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Angiopoietin-related protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 2/3 complex subunit 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 2/3 complex subunit 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MD-2-related lipid-recognition domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MD-2-related lipid-recognition domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myosin light chain kinase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myosin light chain kinase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L24e-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L24e-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coproporphyrinogen III oxidase, oxygen-independent related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coproporphyrinogen III oxidase, oxygen-independent related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Deoxycytidylate deaminase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Deoxycytidylate deaminase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inositol polyphosphate-related phosphatase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inositol polyphosphate-related phosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fumarylacetoacetase, C-terminal-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fumarylacetoacetase, C-terminal-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Agmatinase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Agmatinase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myb-related protein B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myb-related protein B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myb-related protein A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myb-related protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Luc7-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Luc7-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gamma-crystallin-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gamma-crystallin-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PIK-related kinase, FATC Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PIK-related kinase, FATC protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 2/3 complex subunit 5-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 2/3 complex subunit 5-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Parathyroid hormone-related protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Parathyroid hormone-related protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Immunity-related GTPases-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Immunity-related GTPases-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein T2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein T2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein T3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein T3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fos-related antigen 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fos-related antigen 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fos-related antigen 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fos-related antigen 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Beta-lactamase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Beta-lactamase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Allergen V5/Tpx-1-related, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Allergen V5/Tpx-1-related, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription elongation factor, TFIIS-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription elongation factor, TFIIS-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Formyl peptide receptor-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Formyl peptide receptor-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Methyltransferase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Methyltransferase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TB2/DP1/HVA22-related protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TB2/DP1/HVA22-related protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oestrogen-related receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oestrogen-related receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ras-related protein Ral Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ras-related protein Ral protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, dynein-related, AAA domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, dynein-related, AAA domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

AIR synthase-related protein, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the AIR synthase-related protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Patatin/Phospholipase A2-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Patatin/Phospholipase A2-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

StAR-related lipid transfer protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the StAR-related lipid transfer protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Plasminogen-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Plasminogen-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transforming growth factor-beta-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transforming growth factor-beta-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mas-related G protein-coupled receptor F Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mas-related G protein-coupled receptor F protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PIK-related kinase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PIK-related kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 11 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 16 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lipid phosphate phosphatase-related protein type 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipid phosphate phosphatase-related protein type 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lipid phosphate phosphatase-related protein type 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipid phosphate phosphatase-related protein type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lipid phosphate phosphatase-related protein type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipid phosphate phosphatase-related protein type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lipid phosphate phosphatase-related protein type 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipid phosphate phosphatase-related protein type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lipid phosphate phosphatase-related protein type 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipid phosphate phosphatase-related protein type 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 3, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 3, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

3-hydroxyisobutyrate dehydrogenase-related, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 3-hydroxyisobutyrate dehydrogenase-related, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TMP21-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TMP21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Clathrin, heavy chain-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Clathrin, heavy chain-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mas-related G protein-coupled receptor G Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mas-related G protein-coupled receptor G protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mas-related G protein-coupled receptor D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mas-related G protein-coupled receptor D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UV radiation resistance protein/autophagy-related protein 14 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UV radiation resistance protein/autophagy-related protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin receptor-related protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin receptor-related protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor TFIIIC, tau55-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor TFIIIC, tau55-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dopamine beta-hydroxylase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dopamine beta-hydroxylase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mas-related G protein-coupled receptor X2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mas-related G protein-coupled receptor X2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Biogenesis of lysosome-related organelles complex 1 subunit 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Biogenesis of lysosome-related organelles complex 1 subunit 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein T1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein T1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mas-related G protein-coupled receptor family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mas-related G protein-coupled receptor family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vacuolar protein sorting protein 26 related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vacuolar protein sorting protein 26 related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 9 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fukutin-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fukutin-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cerebellar degeneration-related protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cerebellar degeneration-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CD164-related protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CD164-related protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Spermatid-specific manchette-related protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Spermatid-specific manchette-related protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Autophagy-related protein 3, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Autophagy-related protein 3, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myelin P0 protein related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin P0 protein related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ryanodine receptor-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ryanodine receptor-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dystrophin-related protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dystrophin-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nuclear factor erythroid 2-related factor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear factor erythroid 2-related factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Signal transduction histidine kinase-related protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Signal transduction histidine kinase-related protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphatidylserine decarboxylase-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphatidylserine decarboxylase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BUD31/G10-related, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the BUD31/G10-related, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bcl-2-related ovarian killer protein Gene Set