Autosomal Dominant Oculocutaneous Albinism

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Results for "Autosomal Dominant Oculocutaneous Albinism": 1001 gene sets

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Autosomal Dominant Oculocutaneous Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Oculocutaneous Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinoidism, Oculocutaneous, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinoidism, Oculocutaneous, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tyrosinase-negative oculocutaneous albinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tyrosinase-negative oculocutaneous albinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tyrosinase-positive oculocutaneous albinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tyrosinase-positive oculocutaneous albinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculocutaneous albinism type 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculocutaneous albinism type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculocutaneous albinism type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculocutaneous albinism type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculocutaneous albinism type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculocutaneous albinism type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculocutaneous albinism type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculocutaneous albinism type 1B from the curated CTD Gene-Disease Associations dataset.
Albinism, Oculocutaneous Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism, Oculocutaneous from the curated CTD Gene-Disease Associations dataset.
Oculocutaneous Albinism, Type IV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculocutaneous Albinism, Type IV from the curated CTD Gene-Disease Associations dataset.
Oculocutaneous albinism type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculocutaneous albinism type 2 from the curated CTD Gene-Disease Associations dataset.
Oculocutaneous albinism type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculocutaneous albinism type 3 from the curated CTD Gene-Disease Associations dataset.
Oculocutaneous albinism type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oculocutaneous albinism type 1 from the curated CTD Gene-Disease Associations dataset.
oculocutaneous albinism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease oculocutaneous albinism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
oculocutaneous albinism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oculocutaneous albinism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
albinism, oculocutaneous Gene Set From GAD Gene-Disease Associations genes associated with the disease albinism, oculocutaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
type ib (yellow) oculocutaneous albinism Gene Set From GAD Gene-Disease Associations genes associated with the disease type ib (yellow) oculocutaneous albinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oculocutaneous albinism Gene Set From GAD Gene-Disease Associations genes associated with the disease oculocutaneous albinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oculocutaneous albinism type 4 Gene Set From GAD Gene-Disease Associations genes associated with the disease oculocutaneous albinism type 4 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oculocutaneous albinism type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease oculocutaneous albinism type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
type i-a (tyrosinase-negative) oculocutaneous albinism Gene Set From GAD Gene-Disease Associations genes associated with the disease type i-a (tyrosinase-negative) oculocutaneous albinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Albinism, Oculocutaneous Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Albinism, Oculocutaneous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{albinism, oculocutaneous, type ii, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {albinism, oculocutaneous, type ii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type vii Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type v Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type v phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, brown oculocutaneous Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, brown oculocutaneous phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type vi Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism, oculocutaneous, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the albinism, oculocutaneous, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
Oculocutaneous Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculocutaneous Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinism, Oculocutaneous Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinism, Oculocutaneous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brown Oculocutaneous Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brown Oculocutaneous Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Yellow Mutant Oculocutaneous Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Yellow Mutant Oculocutaneous Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculocutaneous Albinism, Type Ii, Modifier Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oculocutaneous Albinism, Type Ii, Modifier Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6) pathway from the Reactome Pathways 2024 dataset.
Oculocutaneous albinism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Oculocutaneous albinism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Oculocutaneous albinism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculocutaneous albinism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculocutaneous albinism type IA Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculocutaneous albinism type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculocutaneous albinism type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculocutaneous albinism type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculocutaneous albinism type III Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculocutaneous albinism type III in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculocutaneous albinism type IV Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculocutaneous albinism type IV in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculocutaneous albinism type IB Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculocutaneous albinism type IB in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tyrosinase-positive oculocutaneous albinism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tyrosinase-positive oculocutaneous albinism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oculocutaneous albinism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oculocutaneous albinism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonsyndromic Oculocutaneous Albinism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic Oculocutaneous Albinism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Temperature-sensitive oculocutaneous albinism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Temperature-sensitive oculocutaneous albinism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, from the curated CTD Gene-Disease Associations dataset.
Autosomal Recessive Ocular Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Ocular Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
oculocutaneous Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term oculocutaneous in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Port-Wine Stain With Oculocutaneous Melanosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Port-Wine Stain With Oculocutaneous Melanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopia 21, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia 21, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia 24, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia 24, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Giant axonal neuropathy, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Giant axonal neuropathy, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant, multiple types, with microcornea Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniodiaphyseal dysplasia, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 3, autosomal dominant or recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 30 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant torsion dystonia 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant torsion dystonia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 29 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coronary artery disease, autosomal dominant 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant isolated somatotropin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sick sinus syndrome 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant nocturnal frontal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 4B autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 4B autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, without vestibular involvement, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, without vestibular involvement, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalcemia, autosomal dominant 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalcemia, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalcemia, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalcemia, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalcemia, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalcemia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhegmatogenous retinal detachment, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Keratitis, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Keratitis, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 8, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 8, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, sensory, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, sensory, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteopetrosis autosomal dominant type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopetrosis autosomal dominant type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 72, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 72, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniometaphyseal dysplasia, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniometaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 31, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 31, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set From 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.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set From 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.
Deafness, autosomal dominant nonsyndromic sensorineural 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant nonsyndromic sensorineural 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyskeratosis congenita, autosomal dominant, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dyskeratosis congenita, autosomal dominant, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune polyglandular syndrome type 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune polyglandular syndrome type 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Methionine adenosyltransferase deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Methionine adenosyltransferase deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 22 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, lateral temporal lobe, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, lateral temporal lobe, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 33, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 33, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Klippel-Feil syndrome 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Klippel-Feil syndrome 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 3a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 3a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalcemia, autosomal dominant 1, with bartter syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalcemia, autosomal dominant 1, with bartter syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 4b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 48 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 48 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 41 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Slowed nerve conduction velocity, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Slowed nerve conduction velocity, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyskeratosis congenita autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dyskeratosis congenita autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amelogenesis imperfecta - hypoplastic autosomal dominant - local phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholesterolemia, autosomal dominant, type B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholesterolemia, autosomal dominant, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudohypoaldosteronism type 1 autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudohypoaldosteronism type 1 autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 56 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 56 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia 22, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia 22, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholesterolemia, autosomal dominant, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholesterolemia, autosomal dominant, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dejerine-Sottas syndrome, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dejerine-Sottas syndrome, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wolfram-like syndrome, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wolfram-like syndrome, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal dominant 64 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal dominant 64 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 42, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 42, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant hypophosphatemic rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant hypophosphatemic rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectopia lentis, isolated, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectopia lentis, isolated, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal dominant 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal dominant 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 36, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 36, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 44 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 44 from the curated CTD Gene-Disease Associations dataset.
WOOLLY HAIR, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease WOOLLY HAIR, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 47 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 47 from the curated CTD Gene-Disease Associations dataset.
Filaminopathy, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Filaminopathy, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 25 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 25 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 15 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 10 from the curated CTD Gene-Disease Associations dataset.
DEAFNESS, AUTOSOMAL DOMINANT 27 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL DOMINANT 27 from the curated CTD Gene-Disease Associations dataset.
Hypophosphatemic Rickets, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Sick Sinus Syndrome 2, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sick Sinus Syndrome 2, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Nystagmus 2, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 2, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Coronary Artery Disease, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Nystagmus 4, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 4, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From 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.
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 4, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 4, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Hypercholesterolemia, Autosomal Dominant, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercholesterolemia, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 8, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 31, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 31, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
DEAFNESS, AUTOSOMAL DOMINANT 4A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL DOMINANT 4A from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 42, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 42, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 33, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 33, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Slowed Nerve Conduction Velocity, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Slowed Nerve Conduction Velocity, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 10, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 10, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 5 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 4 from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 3, Autosomal Dominant Lewy Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 3, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.
Polycystic Kidney, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic Kidney, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 5, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 5, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 53 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 53 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 49 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 49 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 9, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 9, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 37, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 37, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Osteopetrosis autosomal dominant type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteopetrosis autosomal dominant type 1 from the curated CTD Gene-Disease Associations dataset.
Craniometaphyseal Dysplasia, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniometaphyseal Dysplasia, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 3, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 3, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia 38, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia 38, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 48 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 48 from the curated CTD Gene-Disease Associations dataset.
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 29, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 29, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
Striatal Degeneration, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatal Degeneration, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 23 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 28 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 28 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 43 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 43 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 6, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 6, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 8, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 8, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Dyskeratosis Congenita, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dyskeratosis Congenita, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 6 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 5 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 9 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 2B from the curated CTD Gene-Disease Associations dataset.
Deafness, autosomal dominant nonsyndromic sensorineural 17 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, autosomal dominant nonsyndromic sensorineural 17 from the curated CTD Gene-Disease Associations dataset.
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 21 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 21 from the curated CTD Gene-Disease Associations dataset.
DEAFNESS, AUTOSOMAL DOMINANT 50 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL DOMINANT 50 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 7 from the curated CTD Gene-Disease Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Ataxia, Spastic, 1, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia, Spastic, 1, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant, Multiple Types 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.
Nystagmus 3, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 3, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Laterality Defects, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Laterality Defects, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
MYOTONIA CONGENITA, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOTONIA CONGENITA, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 from the curated CTD Gene-Disease Associations dataset.
Periodic fever, familial, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 59 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 59 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 52 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 52 from the curated CTD Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
CUTIS LAXA, AUTOSOMAL DOMINANT 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CUTIS LAXA, AUTOSOMAL DOMINANT 1 from the curated CTD Gene-Disease Associations dataset.
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 16 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 16 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 13, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 13, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 11 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 12 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 13 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 18 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 18 from the curated CTD Gene-Disease Associations dataset.
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy 3, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 20 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 20 from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 24 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 24 from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 4, Autosomal Dominant Lewy Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 4, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.
Coronary Artery Disease, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 2A from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
Spastic paraplegia 19, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic paraplegia 19, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 11, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 11, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 36 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 36 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 3B from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 3A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 3A from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 30 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 30 from the curated CTD Gene-Disease Associations dataset.
Deafness, Autosomal Dominant 31 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Autosomal Dominant 31 from the curated CTD Gene-Disease Associations dataset.
autosomal dominant disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autosomal dominant disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
autosomal dominant disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autosomal dominant disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autosomal dominant nonsyndromic deafness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autosomal dominant nonsyndromic deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autosomal dominant microcephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autosomal dominant microcephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulonephritis, iga; iga glomerulonephritides; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal-dominant retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal-dominant retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant coral-like cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant coral-like cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From 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.
polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From 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.
White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
autosomal dominant disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease autosomal dominant disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
autosomal dominant inheritance Gene Set From HPO Gene-Disease Associations genes associated with the autosomal dominant inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autosomal dominant contiguous gene syndrome Gene Set From HPO Gene-Disease Associations genes associated with the autosomal dominant contiguous gene syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sex-limited autosomal dominant Gene Set From HPO Gene-Disease Associations genes associated with the sex-limited autosomal dominant phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autosomal dominant inheritance with maternal imprinting Gene Set From HPO Gene-Disease Associations genes associated with the autosomal dominant inheritance with maternal imprinting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autosomal dominant somatic cell mutation Gene Set From HPO Gene-Disease Associations genes associated with the autosomal dominant somatic cell mutation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Polycystic Kidney, Autosomal Dominant Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Polycystic Kidney, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From 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.
nemaline myopathy 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 8, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 8, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 19 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 18 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 10 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 13 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 12 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 15 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 14 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 17 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 16 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 13, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 13, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 12, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 12, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 4, torsion, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 4, torsion, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
macrothrombocytopenia, autosomal dominant, tubb1-related Gene Set From OMIM Gene-Disease Associations genes associated with the macrothrombocytopenia, autosomal dominant, tubb1-related phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 30 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 30 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 9 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 8 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 1 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 3 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 2 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 5 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 7 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 6 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
striatal degeneration, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the striatal degeneration, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 72, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 72, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalcemia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalcemia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary, autosomal dominant 3 Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary, autosomal dominant 2 Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency 31a, mycobacteriosis, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency 31a, mycobacteriosis, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
{coronary artery disease, autosomal dominant, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {coronary artery disease, autosomal dominant, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 29, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 29, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 22, with hypertrophic cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 22, with hypertrophic cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, late-onset, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
{osteoporosis, early-onset, susceptibility to, autosomal dominant} Gene Set From OMIM Gene-Disease Associations genes associated with the {osteoporosis, early-onset, susceptibility to, autosomal dominant} phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
woolly hair, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to protein s deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 47 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 47 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 19, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 19, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spondylocostal dysostosis 5, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spondylocostal dysostosis 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 33, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 33, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 42, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 42, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, severe congenital 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal dominant 22 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal dominant 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalcemia, autosomal dominant 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalcemia, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia 24, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the myopia 24, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus 2, congenital, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus 2, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 1, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 1, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 37, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 15 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 16 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 10 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 11 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 13 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 18 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
craniodiaphyseal dysplasia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome, autosomal dominant, hypermobility type Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome, autosomal dominant, hypermobility type phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 8/12 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 8/12 phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 36 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 36 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 33 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 33 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 30 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 30 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 31 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 31 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 3b Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 3a Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 3a phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 31 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 31 phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to protein c deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 64 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 64 phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
preauricular tag, isolated, autosomal dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the preauricular tag, isolated, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 58 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 58 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 59 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 59 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 50 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 50 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 52 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 52 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 53 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 53 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 54 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 54 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 56 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 56 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 37, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
robinow syndrome, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the robinow syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 38, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 38, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene Set From OMIM Gene-Disease Associations genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 39, multiple types, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, platelet-type, 16, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, platelet-type, 16, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary, autosomal dominant 1 Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
factor xi deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the factor xi deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia 22, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the myopia 22, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
wolfram-like syndrome, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the wolfram-like syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperekplexia, hereditary 1, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the hyperekplexia, hereditary 1, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
leukodystrophy, adult-onset, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the leukodystrophy, adult-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic ataxia 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic ataxia 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
osteopetrosis, autosomal dominant 1 Gene Set From OMIM Gene-Disease Associations genes associated with the osteopetrosis, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
osteopetrosis, autosomal dominant 2 Gene Set From OMIM Gene-Disease Associations genes associated with the osteopetrosis, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
retinitis pigmentosa 4, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the retinitis pigmentosa 4, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
klippel-feil syndrome 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the klippel-feil syndrome 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 9, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 9, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 6/14/38 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 6/14/38 phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus 7, congenital, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus 7, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
auditory neuropathy, autosomal dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{dyskeratosis congenita, autosomal dominant 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {dyskeratosis congenita, autosomal dominant 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskeratosis congenita, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the dyskeratosis congenita, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskeratosis congenita, autosomal dominant 1 Gene Set From OMIM Gene-Disease Associations genes associated with the dyskeratosis congenita, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskeratosis congenita, autosomal dominant 3 Gene Set From OMIM Gene-Disease Associations genes associated with the dyskeratosis congenita, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
{coronary artery disease, autosomal dominant, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {coronary artery disease, autosomal dominant, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 21 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 23 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 24 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 26 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant 29 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant 29 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
radiation sensitivity/chromosome instability syndrome, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the radiation sensitivity/chromosome instability syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
klippel-feil syndrome 3, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the klippel-feil syndrome 3, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
alport syndrome, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the alport syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hypophosphatemic rickets, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatemic rickets, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant, with peripheral neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 10, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 10, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, neurosensory, without vestibular involvement, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, neurosensory, without vestibular involvement, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudohypoaldosteronism type i, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the pseudohypoaldosteronism type i, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?spastic paraplegia 41, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?spastic paraplegia 41, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalcemia, autosomal dominant, with bartter syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalcemia, autosomal dominant, with bartter syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency 31c, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency 31c, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 3, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia 21, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the myopia 21, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cutis laxa, autosomal dominant 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cutis laxa, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus 3, congenital, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus 3, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 36, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 36, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, sensory, 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, sensory, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency 32a, mycobacteriosis, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency 32a, mycobacteriosis, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?deafness, autosomal dominant 4b Gene Set From OMIM Gene-Disease Associations genes associated with the ?deafness, autosomal dominant 4b phenotype from the curated OMIM Gene-Disease Associations dataset.
?mental retardation, autosomal dominant 11 Gene Set From OMIM Gene-Disease Associations genes associated with the ?mental retardation, autosomal dominant 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 36, with dentinogenesis Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 36, with dentinogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 2a Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 2b Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 21 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 23 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 22 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 25 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 24 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 27 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 28 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 28 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 17 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 3a, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 3a, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 4a Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 4a phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 49 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 49 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 48 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 48 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 43 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 43 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 41 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 41 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 40 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 40 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 44 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 44 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 7 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 5 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 1 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 9 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 20/26 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 20/26 phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 65 Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 65 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia 20, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the myopia 20, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant, 27 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus 4, congenital, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus 4, congenital, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, severe congenital 2, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, severe congenital 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?giant axonal neuropathy 2, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?giant axonal neuropathy 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, autosomal dominant, 28 Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, autosomal dominant, 28 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia 31, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia 31, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, deafness, and narcolepsy, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, deafness, and narcolepsy, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
Autosomal Dominant Retinitis Pigmentosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Retinitis Pigmentosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Hyperinsulinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Hyperinsulinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Craniometaphyseal Dysplasia, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Craniometaphyseal Dysplasia, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Hypocalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Hypocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Osteopetrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Osteopetrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Tubulointerstitial Kidney Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Tubulointerstitial Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Myotubular Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Myotubular Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Macrothrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Macrothrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Lateral Temporal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Lateral Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Compelling Helio Ophthalmic Outburst Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Compelling Helio Ophthalmic Outburst Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Charcot-Marie-Tooth Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Charcot-Marie-Tooth Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Late Onset Parkinson Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Late Onset Parkinson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Autosomal Dominant Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Autosomal Dominant Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Juvenile Parkinson Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Juvenile Parkinson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Parkinsonism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Craniodiaphyseal Dysplasia, Autosomal Dominant (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Craniodiaphyseal Dysplasia, Autosomal Dominant (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slowed Nerve Conduction Velocity, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slowed Nerve Conduction Velocity, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Vitreoretinochoroidopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Vitreoretinochoroidopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Neurohypophyseal Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Neurohypophyseal Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Beta2-Microglobulinic Amyloidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Beta2-Microglobulinic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antley-Bixler Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antley-Bixler Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Onset Autosomal Dominant Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Onset Autosomal Dominant Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypocalcemia, Autosomal Dominant, With Bartter Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypocalcemia, Autosomal Dominant, With Bartter Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Drusen, Radial, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Drusen, Radial, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Hereditary Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Hereditary Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alport Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alport Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Hypophosphatemic Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Hypophosphatemic Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Giant Axonal Neuropathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Giant Axonal Neuropathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Spondylocostal Dysostosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Spondylocostal Dysostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Robinow Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Robinow Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Hypohidrotic Ectodermal Dysplasia Syndrome (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Hypohidrotic Ectodermal Dysplasia Syndrome (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dejerine-Sottas Neuropathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dejerine-Sottas Neuropathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Ichthyosis Vulgaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Ichthyosis Vulgaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Filaminopathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Filaminopathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Megalencephaly, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Megalencephaly, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iron Overload, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iron Overload, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sick Sinus Syndrome 2, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sick Sinus Syndrome 2, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Epidermolysis Bullosa Simplex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Epidermolysis Bullosa Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mediterranean Fever, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metaphyseal Anadysplasia 1, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metaphyseal Anadysplasia 1, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dejerine-Sottas Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dejerine-Sottas Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inclusion Body Myopathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Optic Atrophy Plus Syndrome Gene Set From 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.
Autosomal Dominant Contiguous Gene Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Contiguous Gene Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Keratitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Keratitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatal Degeneration, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatal Degeneration, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autosomal Dominant Primary Hypomagnesemia With Hypocalciuria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autosomal Dominant Primary Hypomagnesemia With Hypocalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25) pathway from the Reactome Pathways 2024 dataset.
Autosomal dominant disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant familial periodic fever Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant familial periodic fever from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant vitreoretinochoroidopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant vitreoretinochoroidopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant nocturnal frontal lobe epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant hypocalcemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant hypocalcemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 29 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Otospondylomegaepiphyseal dysplasia, autosomal dominant Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Otospondylomegaepiphyseal dysplasia, autosomal dominant from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
adult-onset autosomal dominant demyelinating leukodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease adult-onset autosomal dominant demyelinating leukodystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 43 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autosomal dominant disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant polycystic kidney disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant polycystic kidney disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant pseudohypoaldosteronism type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant pseudohypoaldosteronism type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant familial periodic fever Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant familial periodic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant vitreoretinochoroidopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant vitreoretinochoroidopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant hypocalcemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hypocalcemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 65 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 65 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 3A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 3B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 3B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 4A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant auditory neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant auditory neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nocturnal frontal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Alport syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Alport syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant woolly hair Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant woolly hair in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant osteopetrosis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant osteopetrosis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 67 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 67 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant dyskeratosis congenita 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant dyskeratosis congenita 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Wolfram syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Wolfram syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
adult-onset autosomal dominant demyelinating leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease adult-onset autosomal dominant demyelinating leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cutis laxa Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cutis laxa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital stationary night blindness autosomal dominant 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital stationary night blindness autosomal dominant 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Robinow syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Robinow syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia, deafness and narcolepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cerebellar ataxia, deafness and narcolepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant hypocalcemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hypocalcemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 74 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 74 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 77 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 77 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 4B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 4B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant keratosis follicularis spinulosa decalvans Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant keratosis follicularis spinulosa decalvans in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant dyskeratosis congenita 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant dyskeratosis congenita 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant hypophosphatemic rickets Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hypophosphatemic rickets in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant severe congenital neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant severe congenital neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Robinow syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Robinow syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 68 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 68 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant osteopetrosis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant osteopetrosis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cutis laxa 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cutis laxa 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant keratitis-ichthyosis-deafness syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant keratitis-ichthyosis-deafness syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Robinow syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Robinow syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant dyskeratosis congenita 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant dyskeratosis congenita 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant microcephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant microcephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant sensory ataxia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant sensory ataxia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 20 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 Set From 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.
Autosomal dominant limb-girdle muscular dystrophy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 1H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 1H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant craniometaphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant craniometaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital stationary night blindness autosomal dominant 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital stationary night blindness autosomal dominant 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Otospondylomegaepiphyseal dysplasia, autosomal dominant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Otospondylomegaepiphyseal dysplasia, autosomal dominant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant dystrophic epidermolysis bullosa Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant dystrophic epidermolysis bullosa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary autosomal dominant microcephaly 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary autosomal dominant microcephaly 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant thrombophilia due to protein C deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant thrombophilia due to protein C deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant craniodiaphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant craniodiaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nocturnal frontal lobe epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant beta thalassemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant beta thalassemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant thrombophilia due to protein S deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant thrombophilia due to protein S deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant isolated ectopia lentis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant isolated ectopia lentis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant nonsyndromic deafness 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant nonsyndromic deafness 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cutis laxa 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cutis laxa 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant spondyloepiphyseal dysplasia tarda Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant spondyloepiphyseal dysplasia tarda in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Parkinson disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Parkinson disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant vitreoretinochoroidopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant vitreoretinochoroidopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant popliteal pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant popliteal pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant nonsyndromic hearing loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant polycystic liver disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant polycystic liver disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Amelogenesis imperfecta - hypoplastic autosomal dominant - local Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Amelogenesis imperfecta - hypoplastic autosomal dominant - local phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hypophosphatemic rickets Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hypophosphatemic rickets phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant optic atrophy classic form Gene Set From 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.
Autosomal dominant epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant osteopetrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant osteopetrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant polycystic kidney disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant polycystic kidney disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hypocalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hypocalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant medullary cystic kidney disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant medullary cystic kidney disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital stationary night blindness autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital stationary night blindness autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant non-syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant non-syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant isolated somatotropin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant keratitis-ichthyosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant rhegmatogenous retinal detachment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant rhegmatogenous retinal detachment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant Alport syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Alport syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant nocturnal frontal lobe epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant nocturnal frontal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant distal renal tubular acidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From 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.
Autosomal dominant limb-girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant limb-girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant sensory ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant sensory ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant aplasia and myelodysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant aplasia and myelodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant Kenny-Caffey syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Kenny-Caffey syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult-onset autosomal dominant demyelinating leukodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset autosomal dominant demyelinating leukodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset autosomal dominant Alzheimer disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset autosomal dominant Alzheimer disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral autosomal dominant arteriopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral autosomal dominant arteriopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant slowed nerve conduction velocity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant slowed nerve conduction velocity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant Robinow syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Robinow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant titinopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant titinopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant deafness - onychodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant deafness - onychodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hereditary axonal motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hereditary axonal motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant spastic paraplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant spastic paraplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant keratitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant keratitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant familial hypercholesterolemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant pseudohypoaldosteronism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant pseudohypoaldosteronism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant intermediate Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant intermediate Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant striatal neurodegeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant striatal neurodegeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant ichthyosis vulgaris Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant ichthyosis vulgaris phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hyperinsulinism due to SUR1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hyperinsulinism due to SUR1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant retinitis pigmentosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant omodysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant omodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant auditory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ALG9-associated autosomal dominant polycystic kidney disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ALG9-associated autosomal dominant polycystic kidney disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant sideroblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant vibratory urticaria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant vibratory urticaria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant Opitz G/BBB syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Opitz G/BBB syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant neovascular inflammatory vitreoretinopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant neovascular inflammatory vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MME-related autosomal dominant Charcot Marie Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MME-related autosomal dominant Charcot Marie Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant wooly hair Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant wooly hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HTRA1-related autosomal dominant cerebral small vessel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HTRA1-related autosomal dominant cerebral small vessel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant myopathies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant myopathies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ocular albinism, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ocular albinism, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Partial albinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Partial albinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ocular Albinism type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ocular Albinism type 1 from the curated CTD Gene-Disease Associations dataset.
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.
Albinism deafness syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism deafness syndrome from the curated CTD Gene-Disease Associations dataset.
Albinism ocular late onset sensorineural deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism ocular late onset sensorineural deafness from the curated CTD Gene-Disease Associations dataset.
ocular albinism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ocular albinism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ocular albinism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ocular albinism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ocular albinism Gene Set From GAD Gene-Disease Associations genes associated with the disease ocular albinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albinism Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term albinism in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
albinism Gene Set From HPO Gene-Disease Associations genes associated with the albinism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ocular albinism Gene Set From HPO Gene-Disease Associations genes associated with the ocular albinism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial albinism Gene Set From HPO Gene-Disease Associations genes associated with the partial albinism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Albinism Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Albinism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Albinism, Ocular Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Albinism, Ocular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ocular albinism protein, type 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ocular albinism protein, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ocular albinism Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ocular albinism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ocular albinism, type i, nettleship-falls type Gene Set From OMIM Gene-Disease Associations genes associated with the ocular albinism, type i, nettleship-falls type phenotype from the curated OMIM Gene-Disease Associations dataset.
ocular albinism with sensorineural deafness Gene Set From OMIM Gene-Disease Associations genes associated with the ocular albinism with sensorineural deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
waardenburg syndrome/albinism, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the waardenburg syndrome/albinism, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
albinism-deafness syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the albinism-deafness syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
waardenburg syndrome/ocular albinism, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the waardenburg syndrome/ocular albinism, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
tietz albinism-deafness syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the tietz albinism-deafness syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Albinism, Ocular Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinism, Ocular in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ocular Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ocular Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinism, Tyrosinase-Negative Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinism, Tyrosinase-Negative in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinism, Tyrosinase-Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Albinism, Tyrosinase-Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Albinism, Yellow-Mutant Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Albinism, Yellow-Mutant in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
ocular albinism Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ocular albinism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Ocular albinism 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ocular albinism 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ocular albinism 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ocular albinism 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ocular albinism with sensorineural deafness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ocular albinism with sensorineural deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Albinism or congenital nystagmus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Albinism or congenital nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Albinism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Albinism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ocular albinism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ocular albinism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Beta-thalassemia, dominant inclusion body type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Beta-thalassemia, dominant inclusion body type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteogenesis imperfecta with normal sclerae, dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta with normal sclerae, dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chondrodysplasia punctata 2 X-linked dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chondrodysplasia punctata 2 X-linked dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Larsen syndrome, dominant type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant hereditary optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitreoretinochoroidopathy dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitreoretinochoroidopathy dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease dominant intermediate 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant dystrophic epidermolysis bullosa with absence of skin phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked dominant scapuloperoneal myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked dominant scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iridogoniodysgenesis, dominant type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iridogoniodysgenesis, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset.
Scapuloperoneal Myopathy, X-Linked Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset.
HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT from the curated CTD Gene-Disease Associations dataset.
Chondrodysplasia punctata 2, X-linked dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chondrodysplasia punctata 2, X-linked dominant from the curated CTD Gene-Disease Associations dataset.
Beta Thalassemia, Dominant Inclusion Body Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta Thalassemia, Dominant Inclusion Body Type from the curated CTD Gene-Disease Associations dataset.
Iridogoniodysgenesis, dominant type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iridogoniodysgenesis, dominant type from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B from the curated CTD Gene-Disease Associations dataset.
Klippel Feil syndrome dominant type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Klippel Feil syndrome dominant type from the curated CTD Gene-Disease Associations dataset.
Larsen syndrome, dominant type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Larsen syndrome, dominant type from the curated CTD Gene-Disease Associations dataset.
dominant type 1 von willebrand's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant type 1 von willebrand's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant effect on hdl-cholesterol Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant effect on hdl-cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant non-syndromic sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant non-syndromic sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant progressive deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant progressive deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypophosphatemic rickets, x-linked dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease hypophosphatemic rickets, x-linked dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dominant in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
x-linked dominant inheritance Gene Set From HPO Gene-Disease Associations genes associated with the x-linked dominant inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hypophosphatemic Rickets, X-Linked Dominant Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypophosphatemic Rickets, X-Linked Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
charcot-marie-tooth disease, dominant intermediate f Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate f phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate e Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate e phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate d Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate d phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate c Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate c phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate b Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate b phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate a Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate a phenotype from the curated OMIM Gene-Disease Associations dataset.
thalassemia-beta, dominant inclusion-body Gene Set From OMIM Gene-Disease Associations genes associated with the thalassemia-beta, dominant inclusion-body phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, x-linked dominant, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, x-linked dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
l-ferritin deficiency, dominant and recessive Gene Set From OMIM Gene-Disease Associations genes associated with the l-ferritin deficiency, dominant and recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
chondrodysplasia punctata, x-linked dominant Gene Set From OMIM Gene-Disease Associations genes associated with the chondrodysplasia punctata, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
aicardi-goutieres syndrome 1, dominant and recessive Gene Set From OMIM Gene-Disease Associations genes associated with the aicardi-goutieres syndrome 1, dominant and recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
bernard-soulier syndrome, type a2 (dominant) Gene Set From OMIM Gene-Disease Associations genes associated with the bernard-soulier syndrome, type a2 (dominant) phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal myopathy, x-linked dominant Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal myopathy, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypophosphatemic rickets, x-linked dominant Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatemic rickets, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonia congenita, dominant Gene Set From OMIM Gene-Disease Associations genes associated with the myotonia congenita, dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
weill-marchesani syndrome 2, dominant Gene Set From OMIM Gene-Disease Associations genes associated with the weill-marchesani syndrome 2, dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
Dominant Sensorineural Hearing Loss Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Protoporphyria, Erythropoietic, X-Linked Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Protoporphyria, Erythropoietic, X-Linked Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Myopathy, X-Linked Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Hereditary Optic Atrophy Gene Set From 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.
Alport Syndrome, Dominant Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alport Syndrome, Dominant Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Dystrophic Epidermolysis Bullosa, Albopapular Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Dystrophic Epidermolysis Bullosa, Albopapular Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Beta-Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Beta-Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Drusen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Drusen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Beta Thalassemia, Dominant Inclusion Body Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Beta Thalassemia, Dominant Inclusion Body Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Beta-Plus-Thalassemia, Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Beta-Plus-Thalassemia, Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acroosteolysis Dominant Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acroosteolysis Dominant Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Dominant Inheritance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype X-Linked Dominant Inheritance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
unbalanced complete atrioventricular canal, left dominant Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unbalanced complete atrioventricular canal, left dominant phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
X-linked dominant disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked dominant disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked dominant disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked dominant disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dominant optic atrophy plus syndrome Gene Set From 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.
X-linked dominant hypophosphatemic rickets Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked dominant hypophosphatemic rickets in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked dominant 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked dominant 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked dominant 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked dominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease dominant intermediate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BEST1-related dominant retinopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BEST1-related dominant retinopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dominant hypophosphatemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dominant hypophosphatemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease X-linked dominant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease X-linked dominant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chondrodysplasia punctata 2 X-linked dominant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chondrodysplasia punctata 2 X-linked dominant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dominant beta-thalassemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dominant beta-thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ACTL6B-related dominant intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTL6B-related dominant intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked dominant chondrodysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked dominant chondrodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Parkinson's disease motor subtype (tremor dominant vs postural instability/gait difficulty) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease motor subtype (tremor dominant vs postural instability/gait difficulty) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Short stature, idiopathic, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Methionine adenosyltransferase deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ocular coloboma, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ocular coloboma, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly 12, primary, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 12, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Agammaglobulinemia 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Agammaglobulinemia 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 101 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 101 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 103 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 103 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia due to protein S deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive cutis laxa type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive cutis laxa type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auditory neuropathy, autosomal recessive, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auditory neuropathy, autosomal recessive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholesterolemia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholesterolemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alport syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, autosomal recessive 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, autosomal recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectopia lentis, isolated autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectopia lentis, isolated autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary hypertrophic osteoarthropathy, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary hypertrophic osteoarthropathy, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypophosphatemic bone disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory bowel disease 25, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory bowel disease 25, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 30 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 37 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 37 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 35 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 39 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteopetrosis, autosomal recessive 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopetrosis, autosomal recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 46, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 46, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 48, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 48, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tetraamelia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tetraamelia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 22 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 29 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary autosomal recessive microcephaly 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 59 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 59 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lymphoproliferative syndrome, ebv-associated, autosomal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lymphoproliferative syndrome, ebv-associated, autosomal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Heterotaxy, visceral, 4, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Heterotaxy, visceral, 4, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoglobinuria, acute recurrent, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia autosomal recessive 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia autosomal recessive 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 6, autosomal recessive early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amyotrophic lateral sclerosis 1, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amyotrophic lateral sclerosis 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 3, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hydrocephalus, nonsyndromic, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hydrocephalus, nonsyndromic, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 54, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 54, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia, spastic, 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia, spastic, 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly 10, primary, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 10, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Heterotopia, periventricular, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Heterotopia, periventricular, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Persistent hyperplastic primary vitreous, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Persistent hyperplastic primary vitreous, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 11, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 11, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 57, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 57, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia, autosomal recessive 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 102 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 102 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Heterotaxy, visceral, 2, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Heterotaxy, visceral, 2, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spastic paraplegia 72, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spastic paraplegia 72, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Segawa syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Segawa syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia 23, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia 23, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Klippel-Feil syndrome 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Klippel-Feil syndrome 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, autosomal recessive 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, autosomal recessive 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

Autosomal Dominant Oculocutaneous Albinism Gene Set

Albinoidism, Oculocutaneous, Autosomal Dominant Gene Set

Tyrosinase-negative oculocutaneous albinism Gene Set

Tyrosinase-positive oculocutaneous albinism Gene Set

Oculocutaneous albinism type 7 Gene Set

Oculocutaneous albinism type 3 Gene Set

Oculocutaneous albinism type 4 Gene Set

Oculocutaneous albinism type 1B Gene Set

Albinism, Oculocutaneous Gene Set

Oculocutaneous Albinism, Type IV Gene Set

Oculocutaneous albinism type 2 Gene Set

Oculocutaneous albinism type 3 Gene Set

Oculocutaneous albinism type 1 Gene Set

oculocutaneous albinism Gene Set

oculocutaneous albinism Gene Set

albinism, oculocutaneous Gene Set

type ib (yellow) oculocutaneous albinism Gene Set

oculocutaneous albinism Gene Set

oculocutaneous albinism type 4 Gene Set

oculocutaneous albinism type 2 Gene Set

type i-a (tyrosinase-negative) oculocutaneous albinism Gene Set

Albinism, Oculocutaneous Gene Set

{albinism, oculocutaneous, type ii, modifier of} Gene Set

albinism, oculocutaneous, type vii Gene Set

albinism, oculocutaneous, type iv Gene Set

albinism, oculocutaneous, type ia Gene Set

albinism, oculocutaneous, type ii Gene Set

albinism, oculocutaneous, type v Gene Set

albinism, oculocutaneous, type ib Gene Set

albinism, brown oculocutaneous Gene Set

albinism, oculocutaneous, type vi Gene Set

albinism, oculocutaneous, type iii Gene Set

Oculocutaneous Albinism Gene Set

Albinism, Oculocutaneous Gene Set

Brown Oculocutaneous Albinism Gene Set

Yellow Mutant Oculocutaneous Albinism Gene Set

Oculocutaneous Albinism, Type Ii, Modifier Of Gene Set

Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6) Gene Set

Oculocutaneous albinism Gene Set

Oculocutaneous albinism Gene Set

Oculocutaneous albinism type IA Gene Set

Oculocutaneous albinism type II Gene Set

Oculocutaneous albinism type III Gene Set

Oculocutaneous albinism type IV Gene Set

Oculocutaneous albinism type IB Gene Set

Tyrosinase-positive oculocutaneous albinism Gene Set

Oculocutaneous albinism Gene Set

Nonsyndromic Oculocutaneous Albinism Gene Set

Temperature-sensitive oculocutaneous albinism Gene Set

DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, Gene Set

Autosomal Recessive Ocular Albinism Gene Set

oculocutaneous Gene Set

Port-Wine Stain With Oculocutaneous Melanosis Gene Set

Myopia 21, autosomal dominant Gene Set

Myopia 24, autosomal dominant Gene Set

Congenital myotonia, autosomal dominant form Gene Set

Deafness, autosomal dominant 4 Gene Set

Deafness, autosomal dominant 5 Gene Set

Giant axonal neuropathy, autosomal dominant Gene Set

Cataract, autosomal dominant, multiple types, with microcornea Gene Set

Craniodiaphyseal dysplasia, autosomal dominant Gene Set

Nemaline myopathy 3, autosomal dominant or recessive Gene Set

Mental retardation, autosomal dominant 30 Gene Set

Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set

Mental retardation, autosomal dominant 24 Gene Set

Mental retardation, autosomal dominant 28 Gene Set

Autosomal dominant torsion dystonia 4 Gene Set

Mental retardation, autosomal dominant 23 Gene Set

Mental retardation, autosomal dominant 27 Gene Set

Mental retardation, autosomal dominant 29 Gene Set

Spastic paraplegia 4, autosomal dominant Gene Set

Coronary artery disease, autosomal dominant 2 Gene Set

Congenital stationary night blindness, autosomal dominant 3 Gene Set

Autosomal dominant isolated somatotropin deficiency Gene Set

Sick sinus syndrome 2, autosomal dominant Gene Set

Autosomal dominant nocturnal frontal lobe epilepsy Gene Set

Ceroid lipofuscinosis neuronal 4B autosomal dominant Gene Set

Deafness, without vestibular involvement, autosomal dominant Gene Set

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set