Mixed Sclerosing Bone Dystrophy

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Results for "Mixed Sclerosing Bone Dystrophy": 1001 gene sets

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Mixed Sclerosing Bone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Sclerosing Bone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
sost-related sclerosing bone dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sost-related sclerosing bone dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
SOST-related sclerosing bone dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease SOST-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
SOST-related sclerosing bone dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SOST-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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.
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholangitis, Sclerosing from the curated CTD Gene-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Cholangitis, Sclerosing in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
sclerosing liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pulmonary sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute sclerosing panencephalitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sclerosing hepatic carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cirrhosis, biliary primary; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ulcerative colitis; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease ulcerative colitis; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary sclerosing cholangitis Gene Set From GAD Gene-Disease Associations genes associated with the disease primary sclerosing cholangitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panencephalitis, subacute sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease panencephalitis, subacute sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sclerosing Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term sclerosing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sclerosing cholangitis and ulcerative colitis (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sclerosing cholangitis and ulcerative colitis (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sclerosing cholangitis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sclerosing cholangitis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Subacute Sclerosing Panencephalitis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Subacute Sclerosing Panencephalitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cholangitis, Sclerosing Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cholangitis, Sclerosing phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
cholangitis, primary sclerosing Gene Set From OMIM Gene-Disease Associations genes associated with the cholangitis, primary sclerosing phenotype from the curated OMIM Gene-Disease Associations dataset.
keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set From OMIM Gene-Disease Associations genes associated with the keratosis linearis with ichthyosis congenita and sclerosing keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Gene Set From OMIM Gene-Disease Associations genes associated with the ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis phenotype from the curated OMIM Gene-Disease Associations dataset.
Cholangitis, Sclerosing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cholangitis, Sclerosing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Cholangitis, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Cholangitis, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Sclerosing Panencephalitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Sclerosing Panencephalitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Sclerosing Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Sclerosing Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Igg4-Related Sclerosing Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Igg4-Related Sclerosing Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Igg4-Related Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Igg4-Related Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Polycystic Adenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Polycystic Adenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Peritonitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Epithelioid Fibrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Epithelioid Fibrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breast Sclerosing Adenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breast Sclerosing Adenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spindle Cell/Sclerosing Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spindle Cell/Sclerosing Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Lymphocytic Lobulitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Lymphocytic Lobulitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Sclerosing Sialadenitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Sclerosing Sialadenitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Encapsulating Peritonitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Encapsulating Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Sclerosing Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Sclerosing Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing cholangitis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sclerosing cholangitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary sclerosing cholangitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary sclerosing cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute sclerosing panencephalitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulmonary sclerosing hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing hepatic carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nonencapsulated sclerosing carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nonencapsulated sclerosing carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sclerosing liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated neonatal sclerosing cholangitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated neonatal sclerosing cholangitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal ichthyosis-sclerosing cholangitis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal ichthyosis-sclerosing cholangitis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sclerosing poikiloderma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sclerosing poikiloderma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sclerosing cholangitis and ulcerative colitis (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sclerosing cholangitis and ulcerative colitis (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Autoimmune hepatitis in primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autoimmune hepatitis in primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Liver transplant-free survival in primary sclerosing cholangitis (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver transplant-free survival in primary sclerosing cholangitis (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cholangiocarcinoma in primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholangiocarcinoma in primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cholangiocarcinoma in primary sclerosing cholangitis (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholangiocarcinoma in primary sclerosing cholangitis (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Colorectal carcinoma in primary sclerosing cholangitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal carcinoma in primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
bone resorption; fractures, bone Gene Set From GAD Gene-Disease Associations genes associated with the disease bone resorption; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone density; bone responsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease bone density; bone responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
low bone-mineral density and rapid postmenopausal bone loss Gene Set From GAD Gene-Disease Associations genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal bone mineralization involved in bone maturation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone mineralization involved in bone maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
negative regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
Mixed Tumor, Mullerian Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mixed Tumor, Mullerian from the curated CTD Gene-Disease Associations dataset.
Polyposis Syndrome, Hereditary Mixed, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 from the curated CTD Gene-Disease Associations dataset.
mixed type thymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed type thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed testicular germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
uterine body mixed cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uterine body mixed cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed connective tissue disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed connective tissue disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed lacrimal gland cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed lacrimal gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed germ cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung mixed small cell and squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed hepatoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed hepatoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed cell adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed cell adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed germ cell-sex cord neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed germ cell-sex cord neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed ductal-endocrine carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed ductal-endocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eccrine mixed tumor of skin Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eccrine mixed tumor of skin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed cell type cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed cell type cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hodgkin's lymphoma, mixed cellularity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hodgkin's lymphoma, mixed cellularity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed-type liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed-type liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed endometrial stromal and smooth muscle tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed gonadal dysgenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
granuloma; mixed connective tissue disease; sarcoidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease granuloma; mixed connective tissue disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; mixed connective tissue disease Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; mixed connective tissue disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autologous mixed lymphocyte reaction Gene Set From GAD Gene-Disease Associations genes associated with the disease autologous mixed lymphocyte reaction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mixed polyneuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mixed polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mixed Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mixed in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
DOT1L_DELETION_GDS4295_427_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 5 days Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DOT1L_DELETION_GDS4295_427_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 5 days gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Dot1l_DELETION_GDS4295_426_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 3 days Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Dot1l_DELETION_GDS4295_426_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 3 days gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
DOT1L_DELETION_GDS4295_428_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 7 days Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DOT1L_DELETION_GDS4295_428_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 7 days gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
mixed respiratory and metabolic acidosis Gene Set From HPO Gene-Disease Associations genes associated with the mixed respiratory and metabolic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mixed hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the mixed hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mixed hypo- and hyperpigmentation of the skin Gene Set From HPO Gene-Disease Associations genes associated with the mixed hypo- and hyperpigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mixed demyelinating and axonal polyneuropathy Gene Set From HPO Gene-Disease Associations genes associated with the mixed demyelinating and axonal polyneuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mixed Connective Tissue Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mixed Connective Tissue Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hearing Loss, Mixed Conductive-Sensorineural Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Mixed Conductive-Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neoplasms, Complex and Mixed Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Complex and Mixed phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
mixed cellular infiltration to dermis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mixed cellular infiltration to dermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
polyposis syndrome, hereditary mixed, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the polyposis syndrome, hereditary mixed, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
leukemia, myeloid/lymphoid or mixed-lineage Gene Set From OMIM Gene-Disease Associations genes associated with the leukemia, myeloid/lymphoid or mixed-lineage phenotype from the curated OMIM Gene-Disease Associations dataset.
Mixed Gene Set From ProteomicsDB Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in Mixed relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.
malignant mixed muellerian tumor cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue malignant mixed muellerian tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Mixed Cryoglobulinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Cryoglobulinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Lineage Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Lineage Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Phenotype Acute Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Phenotype Acute Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Anxiety And Depressive Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Anxiety And Depressive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Bipolar I Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Bipolar I Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Salivary Gland Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Salivary Gland Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Gliomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Gliomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Oligoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Astigmatism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Astigmatism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Irritable Bowel Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Irritable Bowel Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Tumor, Mullerian Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Tumor, Mullerian in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Sensory-Motor Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Sensory-Motor Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Hyperlipidemia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Hyperlipidemia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cancer, Embryonal And Mixed Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cancer, Embryonal And Mixed in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Follicular And Papillary Thyroid Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Follicular And Papillary Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neoplasms, Embryonal And Mixed Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neoplasms, Embryonal And Mixed in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Demyelinating And Axonal Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Demyelinating And Axonal Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Oligodendroglioma-Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Oligodendroglioma-Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Mixed-Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Mixed-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Essential Mixed Cryoglobulinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Essential Mixed Cryoglobulinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyposis Syndrome, Hereditary Mixed, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Connective Tissue Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Connective Tissue Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Medullary-Follicular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Medullary-Follicular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Delirium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Delirium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Cell Type Gastrointestinal Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Cell Type Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastrointestinal Mixed Adenoneuroendocrine Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Mixed Adenoneuroendocrine Carcinoma 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.
Malignant Mixed Mesodermal (Mullerian) Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mixed Mesodermal (Mullerian) Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Mixed Salivary Gland Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mixed Salivary Gland Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eccrine Mixed Tumor Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eccrine Mixed Tumor Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Cellularity Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Cellularity Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor, Unclassified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor, Unclassified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Oligodendroglioma-Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Oligodendroglioma-Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Phenotype Acute Leukemia T/Myeloid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Phenotype Acute Leukemia T/Myeloid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Dust Pneumoconiosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Dust Pneumoconiosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Somatotroph And Lactotroph Adenoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Somatotroph And Lactotroph Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Epithelial/Mesenchymal Metaplastic Breast Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Epithelial/Mesenchymal Metaplastic Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Germ Cell Tumour Mixed Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Germ Cell Tumour Mixed in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia; Mixed Dementia; Frontotemporal Dementia Such As Pick'S Disease; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia; Mixed Dementia; Frontotemporal Dementia Such As Pick'S Disease; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Mixed Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Mixed Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Mixed Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mixed Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Type Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Type Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Adenocarcinoma Of The Stomach Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Adenocarcinoma Of The Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Respiratory And Metabolic Acidosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mixed Respiratory And Metabolic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Malignant Mixed Tumor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malignant Mixed Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
mixed cellular infiltration to dermis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the mixed cellular infiltration to dermis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
mixed hearing loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the mixed hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Mixed glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
45,X/46,XY mixed gonadal dysgenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease 45,X/46,XY mixed gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uterine body mixed cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uterine body mixed cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed gonadal dysgenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed testicular germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed germ cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed cell type cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed cell type cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed connective tissue disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed connective tissue disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed germ cell-sex cord neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed germ cell-sex cord neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed phenotype acute leukemia, T/myeloid Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed phenotype acute leukemia, T/myeloid in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lung mixed small cell and squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary mixed polyposis syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed receptive-expressive language disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed receptive-expressive language disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intraocular mixed cell type melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intraocular mixed cell type melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed fibrolamellar hepatocellular carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed fibrolamellar hepatocellular carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hodgkin's lymphoma, mixed cellularity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hodgkin's lymphoma, mixed cellularity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed phenotype acute leukemia, B/myeloid Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed phenotype acute leukemia, B/myeloid in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Endometrial mixed adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial mixed adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed ductal-endocrine carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed ductal-endocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed hepatoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed hepatoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary mixed polyposis syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed cell uveal melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed cell uveal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed oligodendroglioma-astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed oligodendroglioma-astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Eccrine mixed tumor of skin Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eccrine mixed tumor of skin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed epithelial stromal tumour Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed epithelial stromal tumour in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed type thymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed type thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed cell adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed cell adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed cerebral palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed cerebral palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
mixed-type liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease mixed-type liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary mixed polyposis syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed lacrimal gland cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed lacrimal gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed endometrial stromal and smooth muscle tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed type rhabdomyosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed type rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Malignant mixed Muellerian tumor cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Malignant mixed Muellerian tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
X-linked mixed hearing loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked mixed hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mixed Pheno Leukemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mixed Pheno Leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary mixed polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary mixed polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Drug-induced cholestatic/mixed liver injury Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Drug-induced cholestatic/mixed liver injury phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mixed cellularity Hodgkin lymphoma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mixed cellularity Hodgkin lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Smoking status (current vs mixed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Smoking status (current vs mixed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mixed cryoglobulinemia vasculitis in chronic hepatitis C infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mixed cryoglobulinemia vasculitis in chronic hepatitis C infection 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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, 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
congenital muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex Sympathetic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype 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.
Muscular Dystrophy, Facioscapulohumeral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Facioscapulohumeral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myotonic Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myotonic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Duchenne phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myotonic dystrophy protein kinase, coiled coil Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myotonic dystrophy protein kinase, coiled coil protein domain from the InterPro Predicted Protein Domain Annotations dataset.
nail dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nail dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axonal dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
corneal dystrophy, schnyder type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset.
fascioscapulohumeral muscular dystrophy 2, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
newfoundland rod-cone dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the newfoundland rod-cone dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
bothnia retinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, megaconial type Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.
t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, congenital alopecia, and nail dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease 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.
retinal dystrophy, early-onset severe Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract with late-onset corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2c Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, congenital stromal Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, congenital stromal phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lattice type iiia Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type iiia 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.
mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy, x-linked, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, gelatinous drop-like Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, gelatinous drop-like phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-1 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.
miyoshi muscular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 6, 60177 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 6, 60177 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to itga7 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy, limb-girdle, type 2r Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
toenail dystrophy, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, rigid spine, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, epithelial basement membrane Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, epithelial basement membrane phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, merosin-positive Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2q Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2s Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2d Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2g Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2l Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2j Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2j 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.
ullrich congenital muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy and perceptive deafness Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy and perceptive deafness 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.
tibial muscular dystrophy, tardive Gene Set From OMIM Gene-Disease Associations genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinol dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the retinol dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, reis-bucklers type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 3 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.
retinal cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, thiel-behnke type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, thiel-behnke type 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.
cone dystrophy, progressive x-linked, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
choriodal dystrophy, central areolar 2 Gene Set From OMIM Gene-Disease Associations genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonic dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myotonic dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonic dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myotonic dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, endothelial, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 20 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile neuroaxonal dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 3, ar Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
limb-girdle muscular dystrophy, type 1g Gene Set From OMIM Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.
sorsby fundus dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the sorsby fundus dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with rimmed vacuoles Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
bietti crystalline corneoretinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 6, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with epidermolysis bullosa simplex Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lattice type i Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type i 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.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 1, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
becker muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous 2 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, groenouw type i Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
meesmann corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal fleck dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the corneal fleck dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type ic 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.
muscular dystrophy, limb-girdle, type 1e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
?cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 7, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital merosin-deficient Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal cone dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3b Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, avellino type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lisch epithelial Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lisch epithelial 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.
Emery-Dreifuss muscular dystrophy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
myotonic dystrophy type1 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease myotonic dystrophy type1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Bietti Crystalline Corneoretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bietti Crystalline Corneoretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET 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.
Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular 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.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rod-Cone 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.
Myotonic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotonic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obsolete Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obsolete Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Avellino Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Avellino Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophy, Granular Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophy, Granular in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Or Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Or Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiel-Behnke Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiel-Behnke Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eichsfeld Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eichsfeld Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fuchs Endothelial Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lattice Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lattice Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne And Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne And Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Walker-Warburg Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Walker-Warburg Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fukuyama Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fukuyama Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Cervical Sympathetic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Cervical Sympathetic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Schnyder Crystalline Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Schnyder Crystalline Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymorphous Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Corneal 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.
Retinal Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ullrich Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ullrich Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myotonic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myotonic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reflex Sympathetic 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.
Doyne Honeycomb Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doyne Honeycomb Retinal 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.
Autosomal Recessive Limb Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Limb Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy, Tardive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy, Tardive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenintal Hereditary Endothelial Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenintal Hereditary Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jeune Thoracic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jeune Thoracic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mosaic Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mosaic Corneal Dystrophy 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.
Progressive Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Recurrent Erosion Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Recurrent Erosion Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hereditary Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hereditary Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toenail Dystrophy, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
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.
Patterned Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patterned Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Marginal Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Marginal Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intermediate Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intermediate Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe [Duchenne] Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe [Duchenne] Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone Dystrophy With Supernormal Rod Response Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone Dystrophy With Supernormal Rod Response 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.
Pigmentary Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmentary Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Granular Dystrophy, Corneal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Granular Dystrophy, Corneal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreoretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreoretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ocular Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ocular Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Speckled Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Speckled Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pre-Descemet'S Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pre-Descemet'S Corneal 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.
Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pattern Dystrophy Of The Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pattern Dystrophy Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bothnia Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Newfoundland Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Newfoundland Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biallelic Rpe65 Mutation Associated Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biallelic Rpe65 Mutation Associated Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gelatinous Droplike Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gelatinous Droplike Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Basement Membrane Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Basement Membrane Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Groenouw Corneal Dystrophy Type I (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Groenouw Corneal Dystrophy Type I (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Punctate Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Punctate Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reis-Bucklers' Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reis-Bucklers' Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Salzmann Nodular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Salzmann Nodular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophy Of Vulva Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophy Of Vulva 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.
Muscular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nodular Corneal Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nodular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nail dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nail dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purkinje cell axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Purkinje cell axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Affected pathways in Duchenne muscular dystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Affected pathways in Duchenne muscular dystrophy pathway from the WikiPathways Pathways 2024 dataset.
Muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Emery-Dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cone-rod dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Gelatinous drop-like corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gelatinous drop-like corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
epithelial-stromal TGFBI dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease epithelial-stromal TGFBI dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Epithelial and subepithelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Epithelial and subepithelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Lattice corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lattice corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Granular corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Granular corneal dystrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital merosin-deficient muscular dystrophy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Meesmann corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Meesmann corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 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.
Fundus dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fundus dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary retinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fuchs' endothelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fuchs' endothelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Corneal endothelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal endothelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Miyoshi muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy-dystroglycanopathy type A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy-dystroglycanopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Stromal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Stromal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital stromal corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital stromal corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myotonic dystrophy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
T-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease T-cell immunodeficiency, congenital alopecia, and nail dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Tibial muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Tibial muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bietti crystalline corneoretinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy due to LMNA mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cone-rod dystrophy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cone dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cone dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuroaxonal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuroaxonal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation 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.
cone-rod dystrophy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fuchs' endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fuchs' endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Doyne honeycomb retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Doyne honeycomb retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 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 muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
epithelial-stromal TGFBI dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease epithelial-stromal TGFBI dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myotonic dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Lattice corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Asphyxiating thoracic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Schnyder corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Schnyder corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital stromal corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital stromal corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Stromal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Stromal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subepithelial mucinous corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subepithelial mucinous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epithelial and subepithelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial and subepithelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 4 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.
Fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fleck corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fleck corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sorsby's fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sorsby's fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gelatinous drop-like corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gelatinous drop-like corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Meesmann corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Meesmann corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2S Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2S in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Granular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thiel-Behnke corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thiel-Behnke corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal dystrophy with leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal dystrophy with leukodystrophy 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.
Miyoshi muscular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reflex sympathetic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reflex sympathetic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital hereditary endothelial dystrophy of cornea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hereditary endothelial dystrophy of cornea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2M Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2M in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2K Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2K in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital merosin-deficient muscular dystrophy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to LMNA mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polymorphous corneal dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polymorphous corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megaconial type congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megaconial type congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Granular corneal dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal 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.
cone-rod dystrophy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lisch epithelial corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lisch epithelial corneal dystrophy 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.
Corneal dystrophy-perceptive deafness syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal dystrophy-perceptive deafness syndrome 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.
Congenital muscular dystrophy-dystroglycanopathy type A1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior amorphous corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior amorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Granular corneal dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reis-Bucklers corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reis-Bucklers corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polymorphous corneal dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epithelial recurrent erosion dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial recurrent erosion dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type C8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type C8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cone-rod dystrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cone-rod dystrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Harmonizome 3.0

Mixed Sclerosing Bone Dystrophy Gene Set

sost-related sclerosing bone dysplasia Gene Set

sost-related sclerosing bone dysplasia Gene Set

SOST-related sclerosing bone dysplasia Gene Set

SOST-related sclerosing bone dysplasia Gene Set

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

Progressive sclerosing poliodystrophy Gene Set

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

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

Cholangitis, Sclerosing Gene Set

Cholangitis, Sclerosing Gene Set

sclerosing liposarcoma Gene Set

pulmonary sclerosing hemangioma Gene Set

subacute sclerosing panencephalitis Gene Set

sclerosing cholangitis Gene Set

sclerosing keratitis Gene Set

sclerosing hemangioma Gene Set

sclerosing hepatic carcinoma Gene Set

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

cirrhosis, biliary primary; cholangitis, sclerosing Gene Set

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

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

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

ulcerative colitis; cholangitis, sclerosing Gene Set

bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene Set

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

autoimmune diseases; cholangitis, sclerosing Gene Set

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

cholangitis, sclerosing; disease progression Gene Set

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

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

primary sclerosing cholangitis Gene Set

panencephalitis, subacute sclerosing Gene Set

cholangitis, sclerosing; Gene Set

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

subacute sclerosing panencephalitis Gene Set

cholangitis, sclerosing Gene Set

sclerosing Gene Set

Primary sclerosing cholangitis Gene Set

Sclerosing cholangitis and ulcerative colitis (combined) Gene Set

sclerosing cholangitis Gene Set

Subacute Sclerosing Panencephalitis Gene Set

Cholangitis, Sclerosing Gene Set

cholangitis, primary sclerosing Gene Set

keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set

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

Cholangitis, Sclerosing Gene Set

Primary Sclerosing Cholangitis Gene Set

Sclerosing Cholangitis, Neonatal Gene Set

Subacute Sclerosing Panencephalitis Gene Set

Pulmonary Sclerosing Hemangioma Gene Set

Igg4-Related Sclerosing Disease Gene Set

Igg4-Related Sclerosing Cholangitis Gene Set

Sclerosing Polycystic Adenosis Gene Set

Sclerosing Rhabdomyosarcoma Gene Set

Sclerosing Peritonitis Gene Set

Sclerosing Epithelioid Fibrosarcoma Gene Set

Breast Sclerosing Adenosis Gene Set

Sclerosing Hemangioma Gene Set

Spindle Cell/Sclerosing Rhabdomyosarcoma Gene Set

Sclerosing Lymphocytic Lobulitis Gene Set

Secondary Sclerosing Cholangitis Gene Set

Keratosis Linearis With Ichthyosis Congenita And Sclerosing Keratoderma Gene Set

Chronic Sclerosing Sialadenitis Gene Set

Sclerosing Encapsulating Peritonitis Gene Set

Sclerosing Stromal Tumor Gene Set

Ovarian Sclerosing Stromal Tumor Gene Set

Sclerosing cholangitis Gene Set

Sclerosing cholangitis Gene Set

Primary sclerosing cholangitis Gene Set

Subacute sclerosing panencephalitis Gene Set

Sclerosing keratitis Gene Set

Sclerosing hemangioma Gene Set

Pulmonary sclerosing hemangioma Gene Set

Sclerosing hepatic carcinoma Gene Set

Nonencapsulated sclerosing carcinoma Gene Set

Sclerosing liposarcoma Gene Set