| Name |
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Pleoconial Myopathies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pleoconial Myopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitochondrial Myopathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Myopathies from the curated CTD Gene-Disease Associations dataset. |
Myopathies, Structural, Congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathies, Structural, Congenital from the curated CTD Gene-Disease Associations dataset. |
Distal Myopathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal Myopathies from the curated CTD Gene-Disease Associations dataset. |
distal myopathies; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammatory myopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammatory myopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myopathies Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term myopathies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Myopathies, Nemaline Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Myopathies, Nemaline phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Mitochondrial Myopathies Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Mitochondrial Myopathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Myopathies, Structural, Congenital Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Myopathies, Structural, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Idiopathic Inflammatory Myopathies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Inflammatory Myopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myopathies, Nemaline Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myopathies, Nemaline in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Megaconial Myopathies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Megaconial Myopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
ACTA1-related myopathies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTA1-related myopathies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked myopathies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked myopathies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant myopathies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant myopathies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive myopathies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive myopathies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |