| Name |
|---|
OPA6 Geneoptic atrophy 6 (autosomal recessive) |
OPA4 Geneoptic atrophy 4 (autosomal dominant) |
OPA5 Geneoptic atrophy 5 (autosomal dominant) |
OPA2 Geneoptic atrophy 2 (obscure) |
OPA1 Geneoptic atrophy 1 (autosomal dominant) The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017] |
OPA3 Geneoptic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009] |
PBCRA1 Geneprogressive bifocal chorioretinal atrophy 1 |
SPOAN Genespastic paraplegia, optic atrophy, and neuropathy |
CLAM Genecerebellar atrophy with progressive microcephaly |
SMAR GeneSpinal muscular atrophy, chronic distal, autosomal recessive |
SMAL Genespinal muscular atrophy, congenital nonprogressive, of lower limbs |
SCA18 Genespinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy) |
LOAS GeneLeber optic atrophy, susceptibility to |
SMAJ GeneSpinal muscular atrophy, Jokela type |
Acquired Atrophy Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
ovary atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
muscular atrophy, spinal; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipodystrophy, Partial, Acquired Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Partial, Acquired from the curated CTD Gene-Disease Associations dataset. |
Factor 8 deficiency, acquired Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Factor 8 deficiency, acquired from the curated CTD Gene-Disease Associations dataset. |
Acquired angioedema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acquired angioedema from the curated CTD Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acquired Immunodeficiency Syndrome from the curated CTD Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
acquired metabolic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease acquired metabolic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
acquired metabolic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease acquired metabolic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
acquired immunodeficiency syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease acquired immunodeficiency syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
acquired thrombocytopenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired metabolic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired metabolic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired immunodeficiency syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired immunodeficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia, bacterial; pneumonia, viral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, viral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; cardiovascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia, bacterial; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; 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 SetFrom 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. |
acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; Gene SetFrom 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. |
community-acquired pneumonia (cap) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired pneumonia (cap) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aplastic anemia, acquired Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aplastic anemia, acquired in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; substance abuse, intravenous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia; respiratory distress syndrome, adult Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia, bacterial; pneumonia, pneumococcal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, pneumococcal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv seropositivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv seropositivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; sepsis 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 SetFrom 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. |
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction; community-acquired infections; pneumonia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; community-acquired infections; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis Gene SetFrom 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. |
acquired Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term acquired in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Nephrotic syndrome (acquired) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Nephrotic syndrome (acquired) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
acquired metabolic disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease acquired metabolic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
acquired immunodeficiency syndrome Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Community-Acquired Infections Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Community-Acquired Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Simian Acquired Immunodeficiency Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Simian Acquired Immunodeficiency Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Dyslexia, Acquired Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Dyslexia, Acquired phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Acquired Hyperostosis Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Acquired Hyperostosis Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Acquired Immunodeficiency Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
{long qt syndrome 1, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 1, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 2, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome, acquired, reduced susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{lipodystrophy, partial, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {lipodystrophy, partial, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Community Acquired Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Community Acquired Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Camptodactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Camptodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hospital Acquired Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hospital Acquired Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dental Fluorosis, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dental Fluorosis, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Angioedema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Aplastic Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Pectus Carinatum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Pectus Carinatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Kyphoscoliosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Kyphoscoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypogammaglobulinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypogammaglobulinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hallux Valgus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hallux Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Acquired Sideroblastic Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Acquired Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thrombotic Thrombocytopenic Purpura, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thrombotic Thrombocytopenic Purpura, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Porencephaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Porencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Acquired Lymphedema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Acquired Lymphedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Partial Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Partial Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypoparathyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Flat Foot Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Flat Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metabolic Disorder, Central Nervous System, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Disorder, Central Nervous System, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Thrombocytopenia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Nephrogenic Diabetes Insipidus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Nephrogenic Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Phimosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Phimosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypofibrinogenemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypofibrinogenemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Von Willebrand'S Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Von Willebrand'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cubitus Valgus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cubitus Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Acquired Melanosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Melanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypothyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypocalciuric Hypercalcemia, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypocalciuric Hypercalcemia, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Thrombophilia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Thrombophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Obstructive Azoospermia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Acquired Toxoplasmosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Acquired Toxoplasmosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Neuromyotonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Neuromyotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Haemophilia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Haemophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor 8 Deficiency, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor 8 Deficiency, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Clubfoot Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Clubfoot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cystic Kidney Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cystic Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Polyneuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Protein S Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Protein S Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Anomaly Of Tongue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Anomaly Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypophosphatemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypophosphatemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Methemoglobinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Methemoglobinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Deformity Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Deformity Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Platelet Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Platelet Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hospital Acquired Bacterial Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hospital Acquired Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cystic Disease Associated Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cystic Disease Associated Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Renal Cystic Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Renal Cystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Factor Xiii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Factor Xiii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Generalized Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypogonadotropic Hypogonadism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Trigger Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Trigger Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Acquired Nasolacrimal Duct Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Nasolacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Torsion Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cjd Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cjd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Prion Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Prion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Protein C Deficiency, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Protein C Deficiency, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Fanconi Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Fanconi Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Antithrombin Iii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Antithrombin Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired C1 Inhibitor Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired C1 Inhibitor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Communicating Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Communicating Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Factor X Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Factor X Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Meningomyelocele Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Meningomyelocele in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Genu Recurvatum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Genu Recurvatum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Amegakaryocytic Thrombocytopenia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Amegakaryocytic Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Purpura Fulminans Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Purpura Fulminans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired partial lipodystrophy Barraquer Simons syndrome Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Acquired partial lipodystrophy Barraquer Simons syndrome pathway from the WikiPathways Pathways 2024 dataset. |
Acquired metabolic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Acquired metabolic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Acquired metabolic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Acquired metabolic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired immunodeficiency syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Acquired immunodeficiency syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired metabolic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired metabolic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired immunodeficiency syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired immunodeficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired thrombocytopenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired generalized lipodystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired angioedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired angioedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired hyperkeratosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired hyperkeratosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired night blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired von Willebrand syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired von Willebrand syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired gastric outlet stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired gastric outlet stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired laryngomalacia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired laryngomalacia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired tear duct stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired tear duct stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired color blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Leukodystrophy and acquired microcephaly Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukodystrophy and acquired microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired hemoglobin H disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired hemoglobin H disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired partial lipodystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired partial lipodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired polycythemia vera Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired polycythemia vera phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genetic non-acquired premature ovarian failure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic non-acquired premature ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-acquired combined pituitary hormone deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-acquired combined pituitary hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nephrotic syndrome (acquired) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nephrotic syndrome (acquired) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Ovary Gene SetFrom BioGPS Human Cell Type and Tissue Gene Expression Profiles genes with high or low expression in Ovary relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset. |
ovary Gene SetFrom BioGPS Mouse Cell Type and Tissue Gene Expression Profiles genes with high or low expression in ovary relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset. |
Polycystic Ovary Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic Ovary Syndrome from the curated CTD Gene-Disease Associations dataset. |
Polycystic Ovary Syndrome Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Polycystic Ovary Syndrome in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
polycystic ovary syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease polycystic ovary syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
dysgerminoma of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dysgerminoma of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovary serous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovary serous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometriosis of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometriosis of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovary epithelial cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovary epithelial cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
choriocarcinoma of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease choriocarcinoma of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovary transitional cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovary transitional cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrioid ovary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrioid ovary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
polycystic ovary syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease polycystic ovary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dermoid cyst of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dermoid cyst of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovary sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovary sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mature teratoma of the ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mature teratoma of the ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovary adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovary adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
polycystic ovary syndrome; hyperandrogenism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; hyperandrogenism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose intolerance; obesity; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose intolerance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anovulation; infertility, female; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anovulation; infertility, female; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acne vulgaris; hirsutism; hyperandrogenism; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acne vulgaris; hirsutism; hyperandrogenism; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; adrenal androgen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; adrenal androgen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular risk; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular risk; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; diabetes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; obesity; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; glucose; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; glucose; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; obesity; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome (pcos) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome (pcos) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; premature ovarian failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; testosterone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; insulin resistance; overweight; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; overweight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ovary Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term ovary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Polycystic Ovary Syndrome_Skeletal muscle_GSE6798 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Polycystic Ovary Syndrome_Skeletal muscle_GSE6798 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Polycystic Ovary Syndrome_Adipose tissue_GSE5090 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Polycystic Ovary Syndrome_Adipose tissue_GSE5090 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
ovary Gene SetFrom GTEx Tissue Gene Expression Profiles genes with high or low expression in ovary relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. |
Polycystic ovary syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Polycystic ovary syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
polycystic ovary syndrome Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease polycystic ovary syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
ovary Gene SetFrom HPA Tissue Gene Expression Profiles genes with high or low expression in ovary relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. |
ovary Gene SetFrom HPA Tissue Protein Expression Profiles proteins with high or low expression in ovary relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. |
adult ovary Gene SetFrom HPM Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in adult ovary relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset. |
aplasia/hypoplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
streak ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the streak ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Polycystic Ovary Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Polycystic Ovary Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Ovary-specific acidic protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ovary-specific acidic protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Testis and ovary-specific PAZ domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Testis and ovary-specific PAZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal ovary size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent ovary capsule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent ovary capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged ovary Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged ovary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased ovary weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ectopic ovary Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ectopic ovary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary hemorrhage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent ovary Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent ovary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary capsule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased ovary weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ovary Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ovary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased ovary tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased ovary tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
polycystic ovary syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the polycystic ovary syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ovary Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term ovary in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
ovary Gene SetFrom ProteomicsDB Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in ovary relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset. |
Ovary Gene SetFrom Roadmap Epigenomics Cell and Tissue Gene Expression Profiles genes with high or low expression in Ovary relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue Gene Expression Profiles dataset. |
ovary adenocarcinoma cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue ovary adenocarcinoma cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
ovary cancer cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue ovary cancer cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
ovary cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue ovary cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
ovary cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue ovary cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
ovary Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue ovary from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
ovary Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue ovary in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
plant ovary Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue plant ovary in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary cancer cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary epithelium cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary adenocarcinoma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary adenocarcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ovary Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ovary in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Polycystic Ovary Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycystic Ovary Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Serous Cystadenocarcinoma Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Serous Cystadenocarcinoma Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysgerminoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysgerminoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Clear Cell Adenocarcinoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Clear Cell Adenocarcinoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endodermal Sinus Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endodermal Sinus Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chocolate Cyst Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chocolate Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gonadotropin-Resistant Ovary Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gonadotropin-Resistant Ovary Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neoplasm Of Uncertain Or Unknown Behavior Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neoplasm Of Uncertain Or Unknown Behavior Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Torsion Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Torsion Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Ovary And Other Uterine Adnexa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Ovary And Other Uterine Adnexa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrioid Carcinoma Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrioid Carcinoma Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sertoli-Leydig Cell Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sertoli-Leydig Cell Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stromal Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stromal Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Streak Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Streak Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Borderline Epithelial Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Borderline Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Residual Ovary Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Residual Ovary Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid Cell Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid Cell Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Theca Cell Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Theca Cell Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Cell Carcinoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Cell Carcinoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Serous Cystadenoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Serous Cystadenoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Absence Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Cyst Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Epithelial Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucinous Cystadenoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucinous Cystadenoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dermoid Cyst Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dermoid Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epithelial Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Teratoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Teratoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sarcoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sarcoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Low Grade Serous Adenocarcinoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Low Grade Serous Adenocarcinoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Germinal Inclusion Cyst Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Germinal Inclusion Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Epithelial Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Borderline Mucinous Tumour Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Borderline Mucinous Tumour Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycystic Ovary Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Polycystic Ovary Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Small Cell Carcinoma Of The Ovary, Hypercalcemic Type Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Cell Carcinoma Of The Ovary, Hypercalcemic Type in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
SMAD-19615063-OVARY-HUMAN Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the SMAD-19615063-OVARY-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
DMRT1-21621532-FETAL-OVARY Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the DMRT1-21621532-FETAL-OVARY transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
FOXM1-32153563-SKOV3-HUMAN-OVARY-OVARIANCANCER Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the FOXM1-32153563-SKOV3-HUMAN-OVARY-OVARIANCANCER transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
EVI1-22308434-SKOV3-HUMAN-OVARY-OVARIANCANCER Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the EVI1-22308434-SKOV3-HUMAN-OVARY-OVARIANCANCER transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
abnormal ovary morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ectopic ovary Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic ovary phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased ovary secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ovary secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent ovary Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent ovary phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small ovary Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small ovary phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary cyst Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary cyst phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged ovary Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged ovary phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased ovary weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ovary weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary hemorrhage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased ovary tumor incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased ovary tumor incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased ovary weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased ovary weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased ovary adenoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased ovary adenoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased ovary apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased ovary apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased ovary secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased ovary secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary tissue architecture Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary tissue architecture phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal ovary morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
enlarged ovary Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the enlarged ovary phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
small ovary Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the small ovary phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
absent ovary Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the absent ovary phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Ovary Gene SetFrom GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Ovary relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. |
GTEx Ovary 20-29 vs 60-69 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Ovary 20-29 vs 60-69 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Ovary 20-29 vs 50-59 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Ovary 20-29 vs 50-59 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Ovary 20-29 vs 40-49 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Ovary 20-29 vs 40-49 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
Kisspeptin kisspeptin receptor system in the ovary Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Kisspeptin kisspeptin receptor system in the ovary pathway from the WikiPathways Pathways 2024 dataset. |
Polycystic ovary syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Polycystic ovary syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Ovary epithelial cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ovary epithelial cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary adenocarcinoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ovary adenocarcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrioid ovary carcinoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Endometrioid ovary carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polycystic ovary syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Polycystic ovary syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polycystic ovary syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polycystic ovary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary epithelial cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary epithelial cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometriosis of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometriosis of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrioid ovary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrioid ovary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dysgerminoma of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dysgerminoma of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
small-cell carcinoma of the ovary of hypercalcemic type Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease small-cell carcinoma of the ovary of hypercalcemic type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary serous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary serous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mature teratoma of the ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mature teratoma of the ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dermoid cyst of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dermoid cyst of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Choriocarcinoma of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Choriocarcinoma of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immature teratoma of ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immature teratoma of ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myxoid liposarcoma of the ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myxoid liposarcoma of the ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Liposarcoma of the ovary Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Liposarcoma of the ovary in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary transitional cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovary transitional cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovary Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Ovary from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Ovary cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Ovary cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary cancer cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Ovary cancer cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary adenocarcinoma cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Ovary adenocarcinoma cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Ovary in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary adenocarcinoma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary adenocarcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary cancer cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ovary epithelium cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ovary epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Plant ovary Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Plant ovary in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Primary low grade serous adenocarcinoma of ovary Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary low grade serous adenocarcinoma of ovary phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormality of the ovary Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of the ovary phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant germ cell tumor of ovary Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant germ cell tumor of ovary phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polycystic ovary syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Polycystic ovary syndrome (reproductive subtype) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (reproductive subtype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Polycystic ovary syndrome (metabolic subtype) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (metabolic subtype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Polycystic ovary syndrome (indeterminate subtype) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (indeterminate subtype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Polycystic ovary syndrome (adjusted for age) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (adjusted for age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Polycystic ovary syndrome (adjusted for age and BMI) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (adjusted for age and BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Luteinizing hormone levels in polycystic ovary syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Luteinizing hormone levels in polycystic ovary syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Testosterone levels in polycystic ovary syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Testosterone levels in polycystic ovary syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dominant hereditary optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, type II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, X-linked 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked myopathy with postural muscle atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic Atrophy Type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital microvillous atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, autosomal recessive 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sveinsson Chorioretinal Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy, Jerash type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 and deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy with respiratory distress 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset. |
Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset. |
Muscular Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset. |
Myopathy, X-Linked, With Postural Muscle Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset. |
Costeff optic atrophy syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy polyneuropathy deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Chorioretinal atrophy, progressive bifocal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
Gyrate Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset. |
Pigmented Paravenous Chorioretinal Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset. |
OPTIC ATROPHY 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset. |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Muscular Atrophy, Spinal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
adult spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrophy of prostate Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
juvenile spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intermediate spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
skin atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrophy of testis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
partial optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
progressive muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
olivopontocerebellar atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
survival motor neuron spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gyrate atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
choroidal neovascularization; geographic atrophy; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; dementia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; metaplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroidal neovascularization; geographic atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posterior cortical atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
geographic atrophy; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; helicobacter infections; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; prenatal exposure delayed effects; substance-related disorders Gene SetFrom 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. |
brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic disc atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gyrate atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gyrate atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
geographic atrophy; macular degeneration; retinal drusen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blindness; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; choroidal neovascularization; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; aphasia; atrophy; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; multiple sclerosis, relapsing-remitting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastric atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophy phenotype Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber; vision disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; amnesia; atrophy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; stomach atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; epilepsy; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy and moderate deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; huntington disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hippocampal atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonic disorders; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
skeletal muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
striated muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
MRI atrophy measures Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hippocampal atrophy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
muscular atrophy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
motor neuron atrophy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
atrophy/degeneration affecting the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
type 2 muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
levator palpebrae superioris atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral white matter atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the corticospinal tracts Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized limb muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
global brain atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral retinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
caudate atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corpus callosum atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thenar muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pontocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse cerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
brain atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skeletal muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tongue atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
olivopontocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dermal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripapillary chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
subcortical cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse skin atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hand muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
motor neuron atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pelvic girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
leber optic atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral axonal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal pigment epithelial atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fundus atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scapular muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the scapular muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the cerebrum Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
first dorsal interossei muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nonprogressive muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the caudate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic atrophy from cranial nerve compression Gene SetFrom HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar vermis atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
villous atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
iris atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interosseus muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the interosseus muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
type 1 muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
superior rectus atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
noninflammatory macular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized cerebral atrophy/hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
limb-girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
testicular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pigmented paravenous chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peroneal muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontotemporal cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
quadriceps muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
temporal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple System Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Autosomal Dominant Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Muscular Atrophy, Spinal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Muscular Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Geographic Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic atrophy 3-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
dentatorubropallidoluysian atrophy Gene SetFrom KEGG Pathways proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset. |
skeletal muscle fiber atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney cortex atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
testicular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney collecting duct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thymus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
brain atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
optic nerve atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
retinal pigment epithelium atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sebaceous gland atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
midbrain atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal tubule atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
seminal vesicle atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal glomerulus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
meibomian gland atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreatic acinar cell atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
endometrium atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epidermal atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
exocrine pancreas atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spleen atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iris atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vagina atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased susceptibility to induced muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to induced muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vulva atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
oviduct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
external male genitalia atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney medulla atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney papillary atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy-4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy with progressive myoclonic epilepsy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, x-linked 2, infantile Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple system atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, x-linked, with postural muscle atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, chronic distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, jokela type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset. |
sveinsson choreoretinal atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
scapuloperoneal spinal muscular atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, late-onset, finkel type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset. |
dentatorubro-pallidoluysian atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
{spinal muscular atrophy, type iii, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy-7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, lower extremity-predominant 1, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
spastic paraplegia, optic atrophy, and neuropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 2, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
gyrate atrophy of choroid and retina with or without ornithinemia Gene SetFrom OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 3 with cataract Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, x-linked 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented paravenous chorioretinal atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neurodegeneration with optic atrophy, childhood onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal and bulbar muscular atrophy of kennedy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy plus syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, congenital nonprogressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
{leber optic atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Geographic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Geographic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bulbo-Spinal Atrophy, X-Linked Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bulbo-Spinal Atrophy, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retinal Pigment Epithelium Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Linear Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Linear Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Testis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Olivopontocerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Infantile Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Limb Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscle Fiber Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple System Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Motor Neuron Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subcortical Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sveinsson Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sveinsson Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Villous Atrophy Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Progressive Retinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontotemporal Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Cerebral Atrophy/Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dentatorubral-Pallidoluysian Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dentatorubral-Pallidoluysian Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy, Disuse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of The Spinal Cord Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Corpus Callosum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral White Matter Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral White Matter Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Prostate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pelvic Girdle Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pelvic Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy, Muscular, Spinobulbar Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Muscular, Spinobulbar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proliferative Inflammatory Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proliferative Inflammatory Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gyrate Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Distal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy/Degeneration Affecting The Brainstem Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple System Atrophy, Cerebellar Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Optic Disc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebellar Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dominant Hereditary Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Retinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Tongue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paravenous Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pigmented Paravenous Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pigmented Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Limb-Girdle Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Cortical Atrophy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Vagina Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urogenital Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urogenital Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peroneal Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorioretinal Atrophy, Progressive Bifocal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Auditory Neuropathy And Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Skin Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Skin Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Spinal Cord Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spinal Cord Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Splenic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Splenic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Atrophy Of Thyroid Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atrophy Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sporadic Olivopontocerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Axonal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Tongue Papillae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue Papillae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreatic Acinar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Acinar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Retinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Tubular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glaucomatous Atrophy Of Optic Disc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leber Optic Atrophy And Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Seminal Vesicle Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Seminal Vesicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripapillary Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Optic Atrophy Plus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Optic Atrophy Plus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Late Cortical Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rectus Femoris Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rectus Femoris Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Parietal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Parietal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myelopathic Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oculopharyngeal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Proximal Myelopathic Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonprogressive Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodontal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skeletal Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Foveal Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retinal Pigment Epithelial Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hippocampal Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hippocampal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Muscle Atrophy Due To Neurologic Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hand Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shoulder Girdle Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Global Brain Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Global Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Choriocapillaris Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choriocapillaris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mucosal Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mucosal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Villous Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Villous Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Involving The Caudate Nucleus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Caudate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy Of Quadriceps Femoris Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Quadriceps Femoris Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Fiber Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscular Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neurogenic Muscular Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurogenic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple System Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diffuse Cerebral Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy Of The Dentate Nucleus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of The Dentate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corticospinal Tract Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corticospinal Tract Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cerebellar Purkinje Layer Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Purkinje Layer Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cerebellar Vermis Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Involving The Corticospinal Tracts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Extremity Muscle Atrophy, Lower Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extremity Muscle Atrophy, Lower in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Caudate Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
First Dorsal Interossei Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype First Dorsal Interossei Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thenar Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thenar Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diffuse Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy Of Alveolar Ridges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Optic Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Scapular Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scapular Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intrinsic Hand Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrinsic Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pontocerebellar Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tubular Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tubular Atrophy Assessment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy Assessment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripapillary Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tibialis Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tibialis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fundus Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fundus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Levator Palpebrae Superioris Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Levator Palpebrae Superioris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Superior Rectus Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Superior Rectus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Frontal Lobe Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontal Lobe Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Axial Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Involving The Spinal Cord Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy Of Vas Deferens Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Affecting The Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Affecting The Cerebrum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Cerebrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
skeletal muscle atrophy Gene SetFrom GO Biological Process Annotations 2023 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset. |
striated muscle atrophy Gene SetFrom GO Biological Process Annotations 2023 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset. |
muscular atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Meibomian gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the Meibomian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal glomerulus atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
temporal lobe atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal lobe atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
alveolar process atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the alveolar process atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
kidney atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
testicular atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the testicular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thymus atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
spleen atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the spleen atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal tubule atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreatic acinar cell atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lacrimal gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lacrimal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
kidney cortex atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
uterus atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the uterus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
external male genitalia atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
vulva atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the vulva atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
vagina atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the vagina atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
endometrium atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
kidney collecting duct atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
kidney medulla atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thymus cortex atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus cortex atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle fiber atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cerebellum atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebellum atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Leydig cell atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the Leydig cell atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
optic nerve atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
retina pigment epithelium atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the retina pigment epithelium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
seminal vesicle atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
sebaceous gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to induced muscular atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
midbrain atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
epidermal atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
kidney papillary atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
brain atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the brain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
exocrine pancreas atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hippocampus atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
oviduct atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thymus medulla atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus medulla atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
facial muscle atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the facial muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Harderian gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the Harderian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
iris atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the iris atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
gastric gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the gastric gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skin atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skin atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to induced muscular atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lymph node atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lymph node atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small intestinal villus atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small intestinal villus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
forebrain atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the forebrain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
striatum atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the striatum atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
adrenal gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the adrenal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle atrophy Gene SetFrom GO Biological Process Annotations 2025 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset. |
striated muscle atrophy Gene SetFrom GO Biological Process Annotations 2025 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset. |
Spinal muscular atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple system atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple system atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
X-linked spinal muscular atrophy 2 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked spinal muscular atrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Spinal muscular atrophy with lower extremity predominant Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with lower extremity predominant from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Optic atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Optic atrophy 3 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic atrophy 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Spinal muscular atrophy with progressive myoclonic epilepsy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Gyrate atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gyrate atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Skin atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrophy of testis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gyrate atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dominant optic atrophy plus syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dominant optic atrophy plus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple system atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adult spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Scapuloperoneal spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spinal muscular atrophy with progressive myoclonic epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spinal muscular atrophy with lower extremity predominant Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Progressive muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Olivopontocerebellar atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 11 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sveinsson chorioretinal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sveinsson chorioretinal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 10 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intermediate spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 12 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bosch-Boonstra-Schaaf optic atrophy syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bosch-Boonstra-Schaaf optic atrophy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pigmented paravenous chorioretinal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pigmented paravenous chorioretinal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset neurodegeneration with brain atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked distal spinal muscular atrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked spinal muscular atrophy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinal muscular atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Juvenile spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrophy of prostate Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spinal muscular atrophy, Jokela type Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy, Jokela type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Optic atrophy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spinal muscular atrophy type 0 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy type 0 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spinal muscular atrophy with lower extremity predominant 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gyrate atrophy of choroid and retina Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gyrate atrophy of choroid and retina phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple system atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinal pigment epithelial atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal pigment epithelial atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adult-onset proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Scapuloperoneal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant optic atrophy classic form Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant optic atrophy classic form phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
OPA1-related optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the OPA1-related optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pigmented paravenous retinochoroidal atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmented paravenous retinochoroidal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hand muscle atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infantile cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short stature-optic atrophy-Pelger-Huet anomaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-optic atrophy-Pelger-Huet anomaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinal atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bosch-Boonstra-Schaaf optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bosch-Boonstra-Schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Spinocerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Limb-girdle muscle atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital microvillous atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Testicular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Testicular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infantile-onset X-linked spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebral cortical atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cortical atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Auditory neuropathy-optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebral atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Microcornea-myopic chorioretinal atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcornea-myopic chorioretinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Leber optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |