Benign Concentric Annular Macular Dystrophy

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Results for "Benign Concentric Annular Macular Dystrophy": 1002 gene sets

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Benign Concentric Annular Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Concentric Annular Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign concentric annular macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign concentric annular macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macular dystrophy, concentric annular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, concentric annular from the curated CTD Gene-Disease Associations dataset.
concentric Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term concentric in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
concentric hypertrophic cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the concentric hypertrophic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinitis pigmentosa, concentric Gene Set From OMIM Gene-Disease Associations genes associated with the retinitis pigmentosa, concentric phenotype from the curated OMIM Gene-Disease Associations dataset.
Balo'S Concentric Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Balo'S Concentric Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Concentric Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Concentric Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Balo concentric sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Balo concentric sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Concentric hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Concentric hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
annular Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term annular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
annular pancreas Gene Set From HPO Gene-Disease Associations genes associated with the annular pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
annular pancreas Gene Set From MPO Gene-Phenotype Associations gene mutations causing the annular pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Formation of annular gap junctions Gene Set From Reactome Pathways 2014 proteins participating in the Formation of annular gap junctions pathway from the Reactome Pathways dataset.
Annular Erythema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Annular Erythema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Annular Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Annular Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abnormal stapes annular ligament morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal stapes annular ligament morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent stapes annular ligament Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent stapes annular ligament phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
annular pancreas Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the annular pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Formation of annular gap junctions Gene Set From Reactome Pathways 2024 proteins participating in the Formation of annular gap junctions pathway from the Reactome Pathways 2024 dataset.
Annular pancreas Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Annular pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Annular epidermolytic ichthyosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Annular epidermolytic ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
benign prostatic hyperplasia and benign prostatic enlargement Gene Set From GAD Gene-Disease Associations genes associated with the disease benign prostatic hyperplasia and benign prostatic enlargement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Macular dystrophy, vitelliform, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular dystrophy, vitelliform, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Occult macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Occult macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular corneal dystrophy Type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular dystrophy, vitelliform, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular dystrophy, vitelliform, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular dystrophy, retinal, 1, North Carolina type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, atypical vitelliform Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, atypical vitelliform from the curated CTD Gene-Disease Associations dataset.
Macular Dystrophy, Retinal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.
Bullous Dystrophy, Hereditary Macular Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset.
MACULAR DYSTROPHY, RETINAL, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.
OCCULT MACULAR DYSTROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OCCULT MACULAR DYSTROPHY from the curated CTD Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitelliform Macular Dystrophy from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, corneal type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset.
vitelliform macular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
vitelliform macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitelliform macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
occult macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease occult macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular corneal dystrophy. Gene Set From GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinitis pigmentosa; macular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease retinitis pigmentosa; macular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitelliform Macular Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
occult macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypotrichosis, congenital, with juvenile macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the hypotrichosis, congenital, with juvenile macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, north carolina type Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, north carolina type phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, patterned, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, patterned, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy with central cone involvement Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
vitelliform macular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vitelliform macular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
Hereditary Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
North Carolina Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease North Carolina Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Best Vitelliform Macular Dystrophy, Multifocal (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Best Vitelliform Macular Dystrophy, Multifocal (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile-Onset Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile-Onset Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Corneal Dystrophy Type Ii (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy Type Ii (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Butterfly-Shaped Pigmentary Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Butterfly-Shaped Pigmentary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Occult Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occult Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bull'S Eye Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bull'S Eye Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitelliform macular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Macular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vitelliform macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vitelliform macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital hypotrichosis with juvenile macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hypotrichosis with juvenile macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Occult macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Occult macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
North Carolina macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease North Carolina macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Patterned macular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Patterned macular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Patterned macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Patterned macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic disc anomalies with retinal and/or macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic disc anomalies with retinal and/or macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Patterned macular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Patterned macular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Patterned macular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Patterned macular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Occult macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Occult macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vitelliform macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vitelliform macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macular corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macular corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Patterned macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Patterned macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
North Carolina macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the North Carolina macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
becker muscular dystrophy; duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Macular degeneration, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular Degeneration, Age-Related, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 11 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 10 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 9 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 3 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 2 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 1 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 7 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 4 from the curated CTD Gene-Disease Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset.
Hereditary macular coloboma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary macular coloboma from the curated CTD Gene-Disease Associations dataset.
Macular Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Edema from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Macular Degeneration in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
age related macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease age related macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cystoid macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cystoid macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular holes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular holes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetic macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diabetic macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
age related macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular diseases; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroiditis; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroiditis; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydia infections; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydia infections; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; stargardt disease Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; stargardt disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related macular degeneration (wet) Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related macular degeneration (wet) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease wet macular degeneration 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.
blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration, age-related Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration, age-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; neovascularization, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angiomatosis; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease angiomatosis; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; soft drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; soft drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hypertension; macular degeneration; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; inflammation; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; inflammation; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular edema Gene Set From GAD Gene-Disease Associations genes associated with the disease macular edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; cholesterol, hdl; triglycerides; atherosclerosis, coronary; macular degeneration; colorectal cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; cholesterol, hdl; triglycerides; atherosclerosis, coronary; macular degeneration; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; inflammation; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; inflammation; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinopathy, diabetic; macular edema Gene Set From GAD Gene-Disease Associations genes associated with the disease retinopathy, diabetic; macular edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases in twins; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases in twins; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydophila infections; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydophila infections; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; inflammatory bowel diseases; macular degeneration; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; inflammatory bowel diseases; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term macular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Macular degeneration_Fibroblast_GSE1719 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Macular degeneration_Fibroblast_GSE1719 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Age-related macular degeneration (CNV vs. GA) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (GA) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (CNV) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (CNV) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (wet) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (extreme sampling) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
macular degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
age related macular degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease age related macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
age-related macular degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the age-related macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
macular degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
macular hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the macular hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular coloboma Gene Set From HPO Gene-Disease Associations genes associated with the macular coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
linear arrays of macular hyperkeratoses in flexural areas Gene Set From HPO Gene-Disease Associations genes associated with the linear arrays of macular hyperkeratoses in flexural areas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystoid macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystoid macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the macular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular edema Gene Set From HPO Gene-Disease Associations genes associated with the macular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular flecks Gene Set From HPO Gene-Disease Associations genes associated with the macular flecks phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular retinal pigment epithelial mottling Gene Set From HPO Gene-Disease Associations genes associated with the macular retinal pigment epithelial mottling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
age-related macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the age-related macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystoid macular edema Gene Set From HPO Gene-Disease Associations genes associated with the cystoid macular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
noninflammatory macular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macular scarring Gene Set From HPO Gene-Disease Associations genes associated with the progressive macular scarring phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of macular pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of macular pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular scarring Gene Set From HPO Gene-Disease Associations genes associated with the macular scarring phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Macular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Wet Macular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Wet Macular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Macular Edema Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Macular Edema, Cystoid Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Edema, Cystoid phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
utricular macular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
macular degeneration, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 15, suscepbitility to Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 15, suscepbitility to phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 14, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 14, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, neovascular type} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, neovascular type} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, susceptibility to 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, susceptibility to 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{?macular degeneration, age-related} Gene Set From OMIM Gene-Disease Associations genes associated with the {?macular degeneration, age-related} phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, juvenile Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, x-linked atrophic Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, x-linked atrophic phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 7} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 13, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 13, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
Age Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Macular Pigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Macular Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Macular Coloboma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Macular Coloboma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Edema, Cystoid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Edema, Cystoid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wet Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wet Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Holes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Holes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Retinal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Retinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystoid Macular Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystoid Macular Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonexudative Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonexudative Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age-Related Macular Degeneration Type 11 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Macular Degeneration Type 11 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lamellar Macular Hole Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lamellar Macular Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopic Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myopic Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Hyperpigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Clinically Significant Macular Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clinically Significant Macular Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Cutaneous Amyloidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Cutaneous Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Amyloidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Papillorenal Syndrome With Macular Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Papillorenal Syndrome With Macular Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Pseudohole Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Pseudohole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Schisis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Schisis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Hypopigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophic Macular Change Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophic Macular Change in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Drusen Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Drusen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Granular Macular Appearance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Granular Macular Appearance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dry Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dry Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vitelliform-Like Macular Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vitelliform-Like Macular Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Beaten Bronze Macular Sheen Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Beaten Bronze Macular Sheen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hyperautofluorescent Macular Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperautofluorescent Macular Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Macular Morphology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Macular Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Flecks Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Flecks in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foveal Photoreceptor Outer Segment Loss On Macular Oct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Photoreceptor Outer Segment Loss On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Photoreceptor Layer Loss On Macular Oct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Photoreceptor Layer Loss On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Detachment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Linear Arrays Of Macular Hyperkeratoses In Flexural Areas Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Linear Arrays Of Macular Hyperkeratoses In Flexural Areas in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hyporeflective Spaces On Macular Oct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyporeflective Spaces On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Foveal Morphology On Macular Oct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Foveal Morphology On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
utricular macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Age related macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Age related macular degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Macular degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Age related macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cystoid macular edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cystoid macular edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular holes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular holes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked atrophic macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked atrophic macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age related macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal macular morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal macular morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age-related macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MACULAR DEGENERAT Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MACULAR DEGENERAT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Macular telangiectasia type 2 Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Macular telangiectasia type 2 phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Advanced age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Advanced age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exudative age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exudative age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (SNP x mitochondrial G12771A interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (SNP x mitochondrial G12771A interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diabetic macular edema in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic macular edema in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Macular thickness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Macular thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to ranibizumab in age-related macular degeneration (exudative) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ranibizumab in age-related macular degeneration (exudative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (extreme sampling) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (wet) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (choroidal neovascularisation) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (choroidal neovascularisation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (geographic atrophy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (geographic atrophy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (CNV vs. GA) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Laterality in neovascular age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Laterality in neovascular age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neovascular age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neovascular age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression in age-related macular degeneration (adjusted for baseline) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression in age-related macular degeneration (adjusted for baseline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to geographic atrophy form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to geographic atrophy form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to choroidal neovascularization form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to choroidal neovascularization form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to antioxidants and zinc in age-related macular degeneration (disease progression) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antioxidants and zinc in age-related macular degeneration (disease progression) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thrombocytosis, benign familial microcytic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiotensin i-converting enzyme, benign serum increase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiotensin i-converting enzyme, benign serum increase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign recurrent intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyskeratosis, Hereditary Benign Intraepithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dyskeratosis, Hereditary Benign Intraepithelial from the curated CTD Gene-Disease Associations dataset.
Pemphigus, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Histiocytoma, Benign Fibrous Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytoma, Benign Fibrous from the curated CTD Gene-Disease Associations dataset.
Pemphigoid, Benign Mucous Membrane Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigoid, Benign Mucous Membrane from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Benign essential blepharospasm Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Benign essential blepharospasm from the curated CTD Gene-Disease Associations dataset.
Benign Paroxysmal Positional Vertigo Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Benign Paroxysmal Positional Vertigo from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.
Vertigo, Benign Recurrent, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vertigo, Benign Recurrent, 2 from the curated CTD Gene-Disease Associations dataset.
Telangiectasia, Hereditary Benign Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Benign from the curated CTD Gene-Disease Associations dataset.
integumentary system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease integumentary system benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cell type benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cell type benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
organ system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease organ system benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
skin benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease skin benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
organ system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease organ system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
uterine benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease uterine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
female reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
thoracic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign perivascular tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign perivascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gastrointestinal neuroendocrine benign tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hepatobiliary benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatobiliary benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign essential hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bladder benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bladder benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
male reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
musculoskeletal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease musculoskeletal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal neuroendocrine benign tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urinary tract papillary transitional cell benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary tract papillary transitional cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mesenchymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mesenchymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
breast benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
colonic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colonic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
organ system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease organ system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vaginal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vaginal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
uterine benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uterine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urinary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign breast phyllodes tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign breast phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
connective tissue benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease connective tissue benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urethral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urethral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cardiovascular organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign paroxysmal positional nystagmus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign paroxysmal positional nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscle benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscle benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign fibrous mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign fibrous mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gastrointestinal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
kidney benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease kidney benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
integumentary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease integumentary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cell type benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cell type benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign epilepsy with centrotemporal spikes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign epilepsy with centrotemporal spikes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
respiratory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease respiratory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mammary dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mammary dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign pleural mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign pleural mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
female reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peritoneal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peritoneal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sensory organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sensory organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
laryngeal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease laryngeal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
immune system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease immune system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duodenal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duodenal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
endocrine organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endocrine organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bone benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vulvar benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vestibular gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vestibular gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign struma ovarii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign struma ovarii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ureteral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ureteral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign peritoneal mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign peritoneal mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign prostatic hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease benign prostatic hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
benign prostatic hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease benign prostatic hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glossitis, benign migratory Gene Set From GAD Gene-Disease Associations genes associated with the disease glossitis, benign migratory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
benign Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term benign in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
gastrointestinal system benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease gastrointestinal system benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
intestinal benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease intestinal benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
organ system benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease organ system benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
uterine benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease uterine benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
female reproductive organ benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease female reproductive organ benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
reproductive organ benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease reproductive organ benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
benign neoplasm of the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the benign neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
benign neoplasm of the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the benign neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
benign genitourinary tract neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the benign genitourinary tract neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
benign gastrointestinal tract tumors Gene Set From HPO Gene-Disease Associations genes associated with the benign gastrointestinal tract tumors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Glossitis, Benign Migratory Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glossitis, Benign Migratory phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pemphigoid, Benign Mucous Membrane Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pemphigoid, Benign Mucous Membrane phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Benign Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Benign Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
chorea, hereditary benign Gene Set From OMIM Gene-Disease Associations genes associated with the chorea, hereditary benign phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
[fleck retina, familial benign] Gene Set From OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, familial benign Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, familial benign phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, benign familial Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, benign familial phenotype from the curated OMIM Gene-Disease Associations dataset.
epidermolysis bullosa, generalized atrophic benign Gene Set From OMIM Gene-Disease Associations genes associated with the epidermolysis bullosa, generalized atrophic benign phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
vertigo, benign recurrent, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vertigo, benign recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskeratosis, hereditary benign intraepithelial Gene Set From OMIM Gene-Disease Associations genes associated with the dyskeratosis, hereditary benign intraepithelial phenotype from the curated OMIM Gene-Disease Associations dataset.
[angiotensin i-converting enzyme, benign serum increase] Gene Set From OMIM Gene-Disease Associations genes associated with the [angiotensin i-converting enzyme, benign serum increase] phenotype from the curated OMIM Gene-Disease Associations dataset.
{blepharospasm, primary benign} Gene Set From OMIM Gene-Disease Associations genes associated with the {blepharospasm, primary benign} phenotype from the curated OMIM Gene-Disease Associations dataset.
Benign Teratoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Prostatic Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Prostatic Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meningioma, Benign, No Icd-O Subtype Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meningioma, Benign, No Icd-O Subtype in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Recurrent Intrahepatic Cholestasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Recurrent Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Pemphigus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Chondrogenic Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Chondrogenic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Histiocytoma, Benign Fibrous Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histiocytoma, Benign Fibrous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Hereditary Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Hereditary Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorea, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Tumor Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Tumor Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Paroxysmal Positional Vertigo Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Paroxysmal Positional Vertigo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Melanocytic Nevus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Melanocytic Nevus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Ovarian Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Ovarian Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Brain, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Brain, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Thyroid Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Thyroid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cyst Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cyst Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glossitis, Benign Migratory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glossitis, Benign Migratory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Stomach Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leydig Cell Tumor, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leydig Cell Tumor, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Rolandic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Rolandic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Bladder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Adult Familial Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Adult Familial Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Endometrial Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Lung Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Struma Ovarii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Struma Ovarii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hematuria, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pemphigoid, Benign Mucous Membrane Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pemphigoid, Benign Mucous Membrane in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyp Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyp Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Mastocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Mastocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Dermal Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Dermal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Mixed Epithelial And Stromal Tumor Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Mixed Epithelial And Stromal Tumor Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Colon Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Sweat Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Sweat Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Large Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Experimental Organism Benign Basalioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Experimental Organism Benign Basalioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Convulsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Convulsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Epilepsy, Benign, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Epilepsy, Benign, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Prostate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Benign Telangiectasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Benign Telangiectasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Hematuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Hematuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multicystic Mesothelioma, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multicystic Mesothelioma, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Mesial Temporal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Mesial Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neuroendocrine Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neuroendocrine Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synovioma, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Synovioma, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystinosis, Benign, Nonnephropathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystinosis, Benign, Nonnephropathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastric Ulcer Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gastric Ulcer Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Lymphocytic Infiltration Of Jessner Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphocytic Infiltration Of Jessner in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Esophagus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Meninges Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Meninges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Cystic Nephroma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Cystic Nephroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Essential Blepharospasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Essential Blepharospasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Cyst Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Epithelial Tumor Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Vascular Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Vascular Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phosphaturic Mesenchymal Tumor, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phosphaturic Mesenchymal Tumor, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transitional Cell Papilloma, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transitional Cell Papilloma, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Benign Partial Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Benign Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Mesenchymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Mesenchymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endometrial Polyp Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Polyp Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Endometrial Stromal Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Endometrial Stromal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy, Nonfamilial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy, Nonfamilial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Focal Epilepsy, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Focal Epilepsy, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Occipital Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Benign Occipital Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Teratoma Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Teratoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Odontogenic Tumor, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Odontogenic Tumor, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Tumor Of Salivary Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Tumor Of Salivary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Pheochromocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Pheochromocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Adrenal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Lymphoepithelial Lesion Of Lacrimal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphoepithelial Lesion Of Lacrimal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Genitourinary Tract Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Genitourinary Tract Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Experimental Organism Benign Keratoacanthoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Experimental Organism Benign Keratoacanthoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Thyroid Nodule Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Thyroid Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Schwannoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Schwannoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Lymphoproliferative Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphoproliferative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Retina, Familial Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Retina, Familial Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Infantile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Infantile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Supratentorial Neoplasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Supratentorial Neoplasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Pituitary Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Pituitary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Samaritan Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Samaritan Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Testis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Angiotensin I-Converting Enzyme, Benign Serum Increase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Angiotensin I-Converting Enzyme, Benign Serum Increase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Blepharospasm, Benign Essential, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blepharospasm, Benign Essential, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fasciculation, Benign Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fasciculation, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Benign Paroxysmal Torticollis Of Infancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Benign Paroxysmal Torticollis Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Benign Prostatic Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Benign Prostatic Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cancer, Benign Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cancer, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Skin benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Skin benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cell type benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cell type benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Organ system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Organ system benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Integumentary system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Integumentary system benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Pituitary gland benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pituitary gland benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Endocrine organ benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Endocrine organ benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Connective tissue benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Connective tissue benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Musculoskeletal system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Musculoskeletal system benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bone benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bone benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cardiovascular organ benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cardiovascular organ benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neonatal seizures from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign recurrent intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Organ system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Organ system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Female reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Uterine benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Uterine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastrointestinal system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Gastrointestinal system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cell type benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cell type benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Intestinal benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Small intestine benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Small intestine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Integumentary system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Integumentary system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Skin benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Skin benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Endocrine organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Endocrine organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Pituitary gland benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pituitary gland benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign paroxysmal positional vertigo Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign paroxysmal positional vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Organ system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Organ system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cell type benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cell type benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign perivascular tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign perivascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uterine benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uterine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Female reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Endocrine organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endocrine organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cardiovascular organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cardiovascular organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pituitary gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pituitary gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Musculoskeletal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Musculoskeletal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Integumentary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Integumentary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Skin benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skin benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign ileal neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign ileal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastrointestinal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastrointestinal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bone benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bone benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intestinal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Small intestine benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Connective tissue benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Connective tissue benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign vascular tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign vascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Colonic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colonic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Parathyroid gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Parathyroid gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Kidney benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Kidney benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Liver benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Liver benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hepatobiliary benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatobiliary benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Respiratory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Respiratory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Laryngeal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Laryngeal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lung benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lung benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign epilepsy with centrotemporal spikes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign epilepsy with centrotemporal spikes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscle benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscle benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vaginal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vaginal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rectal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rectal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign mammary dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign mammary dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Breast benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thoracic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial hematuria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial hematuria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sweat gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sweat gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign giant cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urinary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Germ cell benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Germ cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Immune system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immune system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Male reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebrovascular benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebrovascular benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, benign infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Biliary tract benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary tract benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripheral nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autonomic nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vulvar benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vulvar benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gallbladder benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gallbladder benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intraductal breast benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intraductal breast benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign breast phyllodes tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign breast phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urinary tract papillary transitional cell benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary tract papillary transitional cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sensory organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign breast adenomyoepithelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign breast adenomyoepithelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rete ovarii benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rete ovarii benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign peritoneal mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign peritoneal mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Eyelid benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eyelid benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ureteral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ureteral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Auditory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urethral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urethral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bladder benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bladder benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal pelvis benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal pelvis benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign essential hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bronchial benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bronchial benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Penile benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Penile benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ampulla of Vater benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ampulla of Vater benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Duodenal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Duodenal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subglottis benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subglottis benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastrointestinal neuroendocrine benign tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastrointestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple benign circumferential skin creases on limbs Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple benign circumferential skin creases on limbs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign pleural mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign pleural mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peritoneal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peritoneal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nasal cavity benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nasal cavity benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fallopian tube benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fallopian tube benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign mastocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign mastocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Frontal sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Frontal sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Paranasal sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Paranasal sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nipple benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nipple benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial benign fleck retina Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial benign fleck retina in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign renovascular hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cecal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cecal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vestibular gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vestibular gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bartholin's gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bartholin's gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cervical benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cervical benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign fibrous mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign fibrous mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign hypertensive renal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign hypertensive renal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign prostatic hyperplasia cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Benign prostatic hyperplasia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign recurrent intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign hereditary chorea Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign hereditary chorea phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cancer or benign tumor Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cancer or benign tumor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign sporadic infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign sporadic infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign neonatal seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign neonatal seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Neonatal Epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Neonatal Epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple benign circumferential skin creases on limbs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple benign circumferential skin creases on limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Rolandic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Rolandic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign cystic nephroma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign cystic nephroma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign childhood epilepsy with centro-temporal spikes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign prostatic hyperplasia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign prostatic hyperplasia and lower urinary tract symptoms Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia and lower urinary tract symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign prostatic hyperplasia and/or lower urinary tract symptoms Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia and/or lower urinary tract symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duchenne muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2S Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2D 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.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bietti crystalline corneoretinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy Type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone dystrophy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thiel-Behnke corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reis-Bucklers' corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy, X-linked 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitelliform dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitelliform dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy Fuchs endothelial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy Fuchs endothelial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schnyder crystalline corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONE DYSTROPHY 5, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONE DYSTROPHY 5, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy type 3A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal endothelial dystrophy type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal endothelial dystrophy type 2 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.
Retinal cone dystrophy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy amelogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 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.
Lattice corneal dystrophy Type III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Groenouw corneal dystrophy type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal epithelial dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal epithelial dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Stromal Corneal Dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miyoshi Muscular Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, gelatinous drop-like Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral muscular dystrophy 1a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 8 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 7 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 5 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy Avellino type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 6 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 13 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Animal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Endothelial, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.
Lattice corneal dystrophy type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Fuchs' endothelial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 2 from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reflex Sympathetic Dystrophy from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Crystalline, of Schnyder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Crystalline, of Schnyder from the curated CTD Gene-Disease Associations dataset.
Scleroatonic muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scleroatonic muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Fuchs' endothelial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Lisch Epithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lisch Epithelial from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, epithelial basement membrane Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, epithelial basement membrane from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy, X-Linked, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy, X-Linked, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Corneal endothelial dystrophy type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal endothelial dystrophy type 2 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 9 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 2 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.
Doyne honeycomb retinal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.
Bietti Crystalline Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bietti Crystalline Dystrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset.
Asphyxiating Thoracic Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Oculopharyngeal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fleck Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fleck from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Merosin-Positive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.
Retinal cone dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby from the curated CTD Gene-Disease Associations dataset.
Myotonic Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myotonic Dystrophy from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy, limb-girdle, type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 7 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 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.
Corneal Dystrophy, Congenital Stromal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
Choroidal dystrophy central areolar Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Thiel-Behnke type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 12 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 11 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 10 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY, X-LINKED, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY, X-LINKED, 1 from the curated CTD Gene-Disease Associations dataset.
Newfoundland Rod-Cone Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Newfoundland Rod-Cone Dystrophy from the curated CTD Gene-Disease Associations dataset.
Groenouw type I corneal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 15 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Lattice Type IIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 5 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 4 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy of Bowman layer, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Lmna-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.
Fuchs Endothelial Dystrophy Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cone-rod dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
asphyxiating thoracic dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lattice corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal granular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal granular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reflex sympathetic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reflex sympathetic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vulvar dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fuchs' endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fuchs' endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease emery-dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
asphyxiating thoracic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bietti crystalline corneoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neuroaxonal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuroaxonal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitreoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitreoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cone dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cone dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
granular corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease granular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fuchs endothelial dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fuchs endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gelatinous droplike corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gelatinous droplike corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic dystrophy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
corneal dystrophies, hereditary; hereditary corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, oculopharyngeal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrioventricular block; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrioventricular block; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease ullrich congenital muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fuchs' endothelial dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fuchs' endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lattice corneal dystrophy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone-rod dystrophy; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease cone-rod dystrophy; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibromyalgia; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fibromyalgia; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recessive cone-rod dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease recessive cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene Set From GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystrophy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dystrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Fuchs's corneal dystrophy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
corneal dystrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease corneal dystrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
nail dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nail dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polymorphous posterior corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the polymorphous posterior corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lattice corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the lattice corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb-girdle muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the cone-rod dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macroreticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macroreticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
granular corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the granular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
map-dot-fingerprint corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the map-dot-fingerprint corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
speckled corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the speckled corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
crystalline corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the crystalline corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the choroidal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
marginal corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the marginal corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nodular corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nodular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive congenital retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
juvenile epithelial corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the juvenile epithelial corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mosaic corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the mosaic corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the punctate corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the reticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Harmonizome 3.0

Benign Concentric Annular Macular Dystrophy Gene Set

Benign concentric annular macular dystrophy Gene Set

Macular dystrophy, concentric annular Gene Set

concentric Gene Set

concentric hypertrophic cardiomyopathy Gene Set

retinitis pigmentosa, concentric Gene Set

Balo'S Concentric Sclerosis Gene Set

Concentric Hypertrophic Cardiomyopathy Gene Set

Balo concentric sclerosis Gene Set

Concentric hypertrophic cardiomyopathy Gene Set

annular Gene Set

annular pancreas Gene Set

annular pancreas Gene Set

Formation of annular gap junctions Gene Set

Annular Erythema Gene Set

Annular Pancreas Gene Set

abnormal stapes annular ligament morphology Gene Set

absent stapes annular ligament Gene Set

annular pancreas Gene Set

Formation of annular gap junctions Gene Set

Annular pancreas Gene Set

Annular epidermolytic ichthyosis Gene Set

benign prostatic hyperplasia and benign prostatic enlargement Gene Set

Macular dystrophy, vitelliform, 5 Gene Set

MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set

Occult macular dystrophy Gene Set

Macular corneal dystrophy Type I Gene Set

Macular dystrophy, vitelliform, 4 Gene Set

Macular dystrophy, retinal, 1, North Carolina type Gene Set

Macular dystrophy, atypical vitelliform Gene Set

Macular Dystrophy, Retinal, 2 Gene Set

Bullous Dystrophy, Hereditary Macular Type Gene Set

MACULAR DYSTROPHY, RETINAL, 3 Gene Set

OCCULT MACULAR DYSTROPHY Gene Set

Vitelliform Macular Dystrophy Gene Set

Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

Macular dystrophy, corneal type 1 Gene Set

vitelliform macular dystrophy Gene Set

vitelliform macular dystrophy Gene Set

occult macular dystrophy Gene Set

macular corneal dystrophy Gene Set

macular corneal dystrophy. Gene Set

retinitis pigmentosa; macular dystrophy Gene Set

macular corneal dystrophy Gene Set

macular dystrophy Gene Set

Vitelliform Macular Dystrophy Gene Set

occult macular dystrophy Gene Set

ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

macular dystrophy, retinal, 3 Gene Set

macular dystrophy, retinal, 2 Gene Set

hypotrichosis, congenital, with juvenile macular dystrophy Gene Set

macular dystrophy, north carolina type Gene Set

macular dystrophy, patterned, 1 Gene Set

macular dystrophy with central cone involvement Gene Set

vitelliform macular dystrophy 2 Gene Set

macular corneal dystrophy Gene Set

macular dystrophy, vitelliform, 5 Gene Set

macular dystrophy, vitelliform, 4 Gene Set

macular dystrophy, vitelliform, 3 Gene Set

Hereditary Macular Dystrophy Gene Set

Macular Dystrophy Gene Set

North Carolina Macular Dystrophy Gene Set

Vitelliform Macular Dystrophy Gene Set

Adult-Onset Vitelliform Macular Dystrophy Gene Set

Best Vitelliform Macular Dystrophy, Multifocal (Disorder) Gene Set

Juvenile-Onset Vitelliform Macular Dystrophy Gene Set

Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set

Retinal Dystrophy With Early Macular Involvement Gene Set

Macular Corneal Dystrophy Gene Set

Macular Corneal Dystrophy Type Ii (Disorder) Gene Set

Butterfly-Shaped Pigmentary Macular Dystrophy Gene Set

Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 Gene Set

Occult Macular Dystrophy Gene Set

Bull'S Eye Macular Dystrophy Gene Set

Macular Dystrophy Gene Set

Vitelliform macular dystrophy Gene Set

Macular corneal dystrophy Gene Set

Vitelliform macular dystrophy Gene Set

Congenital hypotrichosis with juvenile macular dystrophy Gene Set