Myopathy, myosin storage

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Results for "Myopathy, myosin storage": 900 gene sets

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Myopathy, myosin storage Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, myosin storage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, Myosin Storage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Myosin Storage from the curated CTD Gene-Disease Associations dataset.
myopathy, myosin storage Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myosin storage phenotype from the curated OMIM Gene-Disease Associations dataset.
Myosin storage myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myosin storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neutral lipid storage disease with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutral Lipid Storage Disease with Myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset.
neutral lipid storage disease with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the neutral lipid storage disease with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
Neutral Lipid Storage Disease With Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neutral Lipid Storage Disease With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neutral lipid storage myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral lipid storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
pkc-catalyzed phosphorylation of inhibitory phosphoprotein of myosin phosphatase Gene Set From Biocarta Pathways proteins participating in the pkc-catalyzed phosphorylation of inhibitory phosphoprotein of myosin phosphatase pathway from the Biocarta Pathways dataset.
muscle myosin complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the muscle myosin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
myosin vii complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the myosin vii complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
striated muscle myosin thick filament Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the striated muscle myosin thick filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
myosin ii complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the myosin ii complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
myosin i complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the myosin i complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
myosin complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the myosin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
unconventional myosin complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the unconventional myosin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
myosin filament Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the myosin filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
muscle myosin complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the muscle myosin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin iv complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin iv complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin phosphatase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin phosphatase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin vii complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin vii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin xiv complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin xiv complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin viii complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin viii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin ii complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin ii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin xi complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin xi complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin vi complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin vi complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin i complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin i complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin xviii complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin xviii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin v complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin v complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
unconventional myosin complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the unconventional myosin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
myosin filament Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
WIP-WASp-actin-myosin-IIa complex Gene Set From CORUM Protein Complexes proteins in the WIP-WASp-actin-myosin-IIa complex protein complex from the CORUM Protein Complexes dataset.
Rab27a-melanophilin-myosin-Va complex Gene Set From CORUM Protein Complexes proteins in the Rab27a-melanophilin-myosin-Va complex protein complex from the CORUM Protein Complexes dataset.
myosin Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term myosin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of myosin light chain kinase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
striated muscle myosin thick filament assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the striated muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of myosin-light-chain-phosphatase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of myosin-light-chain-phosphatase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of myosin ii filament organization Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of myosin ii filament organization biological process from the curated GO Biological Process Annotations 2015 dataset.
myosin filament organization Gene Set From GO Biological Process Annotations 2015 genes participating in the myosin filament organization biological process from the curated GO Biological Process Annotations 2015 dataset.
actin-myosin filament sliding Gene Set From GO Biological Process Annotations 2015 genes participating in the actin-myosin filament sliding biological process from the curated GO Biological Process Annotations 2015 dataset.
myosin filament assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the myosin filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
skeletal muscle myosin thick filament assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of myosin light chain kinase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
muscle myosin complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the muscle myosin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin vii complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the myosin vii complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin ii filament Gene Set From GO Cellular Component Annotations 2015 proteins localized to the myosin ii filament cellular component from the curated GO Cellular Component Annotations 2015 dataset.
striated muscle myosin thick filament Gene Set From GO Cellular Component Annotations 2015 proteins localized to the striated muscle myosin thick filament cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin ii complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the myosin ii complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin i complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the myosin i complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the myosin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
unconventional myosin complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the unconventional myosin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin filament Gene Set From GO Cellular Component Annotations 2015 proteins localized to the myosin filament cellular component from the curated GO Cellular Component Annotations 2015 dataset.
myosin ii heavy chain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin ii heavy chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin light chain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin light chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin tail binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin tail binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin heavy chain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin heavy chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin v binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin v binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin phosphatase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin phosphatase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin ii binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin ii binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin-light-chain-phosphatase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin-light-chain-phosphatase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin phosphatase regulator activity Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin phosphatase regulator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin head/neck binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin head/neck binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin light chain kinase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin light chain kinase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin vi light chain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin vi light chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
myosin vi binding Gene Set From GO Molecular Function Annotations 2015 genes performing the myosin vi binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Myosin, N-terminal, SH3-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin, N-terminal, SH3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin light chain kinase-related Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin light chain kinase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Telokin/Myosin light chain kinase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Telokin/Myosin light chain kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin tail Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin tail protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Unconventional myosin-XVIIIb Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Unconventional myosin-XVIIIb protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Obscurin-myosin light chain kinase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Obscurin-myosin light chain kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin S1 fragment, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin S1 fragment, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin-like IQ motif-containing domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin-like IQ motif-containing domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin head, motor domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin head, motor domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin tail 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin tail 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Unconventional myosin-IXb Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Unconventional myosin-IXb protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Unconventional myosin-IXa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Unconventional myosin-IXa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myosin-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
myosin Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term myosin in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
negative regulation of myosin-light-chain-phosphatase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of myosin-light-chain-phosphatase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of myosin-light-chain-phosphatase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
skeletal muscle myosin thick filament assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of myosin light chain kinase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
actin-myosin filament sliding Gene Set From GO Biological Process Annotations 2023 genes participating in the actin-myosin filament sliding biological process from the curated GO Biological Process Annotations 2023 dataset.
myosin II filament disassembly Gene Set From GO Biological Process Annotations 2023 genes participating in the myosin II filament disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.
striated muscle myosin thick filament assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the striated muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of myosin light chain kinase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
myosin filament disassembly Gene Set From GO Biological Process Annotations 2023 genes participating in the myosin filament disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.
myosin II filament organization Gene Set From GO Biological Process Annotations 2023 genes participating in the myosin II filament organization biological process from the curated GO Biological Process Annotations 2023 dataset.
muscle myosin complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the muscle myosin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
myosin filament Gene Set From GO Cellular Component Annotations 2023 proteins localized to the myosin filament cellular component from the curated GO Cellular Component Annotations 2023 dataset.
myosin II filament Gene Set From GO Cellular Component Annotations 2023 proteins localized to the myosin II filament cellular component from the curated GO Cellular Component Annotations 2023 dataset.
myosin V complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the myosin V complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
myosin V binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin V binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin VI binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin VI binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin II binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin II binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin II heavy chain binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin II heavy chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin heavy chain binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin heavy chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin phosphatase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin phosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin light chain binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin light chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin-light-chain-phosphatase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin-light-chain-phosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin phosphatase regulator activity Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin phosphatase regulator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin light chain kinase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin light chain kinase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin VI light chain binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin VI light chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin tail binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin tail binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin I binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin I binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin II head/neck binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin II head/neck binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
myosin head/neck binding Gene Set From GO Molecular Function Annotations 2023 genes performing the myosin head/neck binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
skeletal muscle myosin thick filament assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
actin-myosin filament sliding Gene Set From GO Biological Process Annotations 2025 genes participating in the actin-myosin filament sliding biological process from the curated GO Biological Process Annotations 2025 dataset.
myosin II filament disassembly Gene Set From GO Biological Process Annotations 2025 genes participating in the myosin II filament disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.
striated muscle myosin thick filament assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the striated muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
myosin filament disassembly Gene Set From GO Biological Process Annotations 2025 genes participating in the myosin filament disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.
myosin II filament organization Gene Set From GO Biological Process Annotations 2025 genes participating in the myosin II filament organization biological process from the curated GO Biological Process Annotations 2025 dataset.
muscle myosin complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the muscle myosin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
myosin filament Gene Set From GO Cellular Component Annotations 2025 proteins localized to the myosin filament cellular component from the curated GO Cellular Component Annotations 2025 dataset.
myosin II filament Gene Set From GO Cellular Component Annotations 2025 proteins localized to the myosin II filament cellular component from the curated GO Cellular Component Annotations 2025 dataset.
myosin V complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the myosin V complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
myosin V binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin V binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin VI binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin VI binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin II binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin II binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin II heavy chain binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin II heavy chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin heavy chain binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin heavy chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin phosphatase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin phosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin light chain binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin light chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin-light-chain-phosphatase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin-light-chain-phosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin phosphatase regulator activity Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin phosphatase regulator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin light chain kinase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin light chain kinase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin VI light chain binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin VI light chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin head/neck binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin head/neck binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin tail binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin tail binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin I binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin I binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
myosin II head/neck binding Gene Set From GO Molecular Function Annotations 2025 genes performing the myosin II head/neck binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Muscle myosin complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Muscle myosin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Unconventional myosin complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Unconventional myosin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Myosin II filament Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Myosin II filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Myosin II complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Myosin II complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Myosin V complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Myosin V complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Myosin filament Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Myosin filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Striated muscle myosin thick filament Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Striated muscle myosin thick filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Myosin filament Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin II complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin II complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Unconventional myosin complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Unconventional myosin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin VI complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin VI complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin X complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin X complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin phosphatase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin phosphatase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin I complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin I complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XVI complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XVI complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XII complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XV complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XV complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin III complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin III complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin VII complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin VII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin IX complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin IX complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin II filament Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin II filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Muscle myosin complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Muscle myosin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin V complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin V complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin IV complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin IV complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XI complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XI complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Striated muscle myosin thick filament Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Striated muscle myosin thick filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XVIII complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XVIII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XIII complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XIII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XIV complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XIV complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin XVII complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin XVII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Myosin VIII complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin VIII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease type IXa1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IV, congenital neuromuscular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Phytanic acid storage disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Triglyceride storage disease with ichthyosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type II, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease 0, muscle Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease 0, muscle phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type X Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXa2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXa2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cholestanol storage disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IIIa Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease XV Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease XV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXb Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXc Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IIIc Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IIIb Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sialic acid storage disease, severe infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXd Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type V Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
proteasome storage granule Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the proteasome storage granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
storage vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the storage vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
monolayer-surrounded lipid storage body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the monolayer-surrounded lipid storage body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
protein storage vacuole membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the protein storage vacuole membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
protein storage vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the protein storage vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Cholesterol Ester Storage Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholesterol Ester Storage Disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease 0, Liver Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Liver from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease 0, Muscle Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Muscle from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type IV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type IV from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IXB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IXB from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease, Type IXD Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease, Type IXD from the curated CTD Gene-Disease Associations dataset.
GLYCOGEN STORAGE DISEASE IXa1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE IXa1 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease XII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XII from the curated CTD Gene-Disease Associations dataset.
Hepatorenal form of glycogen storage disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatorenal form of glycogen storage disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type III Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type III from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type II from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease XIII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XIII from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type VII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type VII from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IXC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IXC from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IB from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type IIb Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type IIb from the curated CTD Gene-Disease Associations dataset.
Sialic Acid Storage Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sialic Acid Storage Disease from the curated CTD Gene-Disease Associations dataset.
Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset.
GLYCOGEN STORAGE DISEASE XV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE XV from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type I from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease of Heart, Lethal Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IC from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type V Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type V from the curated CTD Gene-Disease Associations dataset.
glycogen storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease vii Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease vii from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cholesterol ester storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cholesterol ester storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease i Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease i from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease v Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease v from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
lysosomal storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lysosomal storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
lipid storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lipid storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
neutral lipid storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neutral lipid storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease iv Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease iv from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease ii Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease ii from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease vi Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen storage disease vi from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
lipid storage disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lipid storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
lysosomal storage disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lysosomal storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease xv Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease xv in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholesterol ester storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cholesterol ester storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease viii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease viii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease iv Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease iv in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease vi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease vi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease iii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease iii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lipid storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
platelet storage pool deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease platelet storage pool deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease vii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease vii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease i Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease v Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease v in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lysosomal storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lysosomal storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease ix Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease ix in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease ii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neutral lipid storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neutral lipid storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen storage disease type ii; heart diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type ii; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type v Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type v in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type i Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acid lipase deficiency and cholesterol ester storage disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acid lipase deficiency and cholesterol ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; glycogen storage disease type i; sickle cell anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; glycogen storage disease type i; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type iii Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type i; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type i; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late-onset glycogen storage disease type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease late-onset glycogen storage disease type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type i; hemolysis; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type i; hemolysis; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type iiia Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type iiia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lysosomal storage disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lysosomal storage disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesteryl ester storage disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesteryl ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
storage Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term storage in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of lipid storage Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset.
cholesterol storage Gene Set From GO Biological Process Annotations 2015 genes participating in the cholesterol storage biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of lipid storage Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of lipid storage Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2015 dataset.
nitric oxide storage Gene Set From GO Biological Process Annotations 2015 genes participating in the nitric oxide storage biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2015 dataset.
lipid storage Gene Set From GO Biological Process Annotations 2015 genes participating in the lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2015 dataset.
cholesterol ester storage disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cholesterol ester storage disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
lipid storage disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease lipid storage disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
lysosomal storage disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease lysosomal storage disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material Gene Set From HPO Gene-Disease Associations genes associated with the intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intracellular accumulation of autofluorescent lipopigment storage material Gene Set From HPO Gene-Disease Associations genes associated with the intracellular accumulation of autofluorescent lipopigment storage material phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
curvilinear intracellular accumulation of autofluorescent lipopigment storage material Gene Set From HPO Gene-Disease Associations genes associated with the curvilinear intracellular accumulation of autofluorescent lipopigment storage material phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fingerprint intracellular accumulation of autofluorescent lipopigment storage material Gene Set From HPO Gene-Disease Associations genes associated with the fingerprint intracellular accumulation of autofluorescent lipopigment storage material phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rectilinear intracellular accumulation of autofluorescent lipopigment storage material Gene Set From HPO Gene-Disease Associations genes associated with the rectilinear intracellular accumulation of autofluorescent lipopigment storage material phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cholesterol Ester Storage Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cholesterol Ester Storage Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glycogen Storage Disease Type II Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glycogen Storage Disease Type II phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glycogen Storage Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glycogen Storage Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glycogen Storage Disease Type III Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glycogen Storage Disease Type III phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glycogen Storage Disease Type V Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glycogen Storage Disease Type V phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glycogen Storage Disease Type I Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glycogen Storage Disease Type I phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fat storage-inducing transmembrane protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Fat storage-inducing transmembrane protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
decreased mast cell protease storage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell protease storage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mast cell histamine storage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell histamine storage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
glycogen storage disease iiia Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease iiia phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease iiib Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease iiib phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease 0, muscle Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease 0, muscle phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease ixc Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease ixc phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease of heart, lethal congenital Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease of heart, lethal congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease 0, liver Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease 0, liver phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease xii Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease xii phenotype from the curated OMIM Gene-Disease Associations dataset.
?glycogen storage disease xiii Gene Set From OMIM Gene-Disease Associations genes associated with the ?glycogen storage disease xiii phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease iv Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease iv phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease ia Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease ia phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease ic Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease ic phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease ib Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease ib phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease ii Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease ii phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease, type ixa2 Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease, type ixa2 phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease, type ixa1 Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease, type ixa1 phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease vi Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease vi phenotype from the curated OMIM Gene-Disease Associations dataset.
?glycogen storage disease xv Gene Set From OMIM Gene-Disease Associations genes associated with the ?glycogen storage disease xv phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease x Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease x phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease xi Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease xi phenotype from the curated OMIM Gene-Disease Associations dataset.
sialic acid storage disorder, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the sialic acid storage disorder, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
glycogen storage disease vii Gene Set From OMIM Gene-Disease Associations genes associated with the glycogen storage disease vii phenotype from the curated OMIM Gene-Disease Associations dataset.
cholesteryl ester storage disease Gene Set From OMIM Gene-Disease Associations genes associated with the cholesteryl ester storage disease phenotype from the curated OMIM Gene-Disease Associations dataset.
Glycogen storage diseases Gene Set From Reactome Pathways 2014 proteins participating in the Glycogen storage diseases pathway from the Reactome Pathways dataset.
storage tissue Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue storage tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Triglyceride Storage Disease With Ichthyosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triglyceride Storage Disease With Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cholesterol Ester Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cholesterol Ester Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glycogen Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glycogen Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Platelet Storage Pool Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Platelet Storage Pool Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Glycogen Storage Disease Of Infants Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Glycogen Storage Disease Of Infants in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sialic Acid Storage Disease, Finnish Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sialic Acid Storage Disease, Finnish Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Glycogen Storage Disease Type Ii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Glycogen Storage Disease Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glycoprotein Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glycoprotein Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
N-Acetylneuraminic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease N-Acetylneuraminic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Free Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Free Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Free Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Free Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sialic Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sialic Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Curvilinear Intracellular Accumulation Of Autofluorescent Lipopigment Storage Material Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Curvilinear Intracellular Accumulation Of Autofluorescent Lipopigment Storage Material in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fingerprint Intracellular Accumulation Of Autofluorescent Lipopigment Storage Material Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fingerprint Intracellular Accumulation Of Autofluorescent Lipopigment Storage Material in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rectilinear Intracellular Accumulation Of Autofluorescent Lipopigment Storage Material Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rectilinear Intracellular Accumulation Of Autofluorescent Lipopigment Storage Material in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Glycogen Storage Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glycogen Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intraaxonal Accumulation Of Curvilinear Autofluorescent Lipopigment Storage Material Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intraaxonal Accumulation Of Curvilinear Autofluorescent Lipopigment Storage Material in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hepatic Glycogen Storage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Glycogen Storage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of lipid storage Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of lipid storage Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset.
lipid transport involved in lipid storage Gene Set From GO Biological Process Annotations 2023 genes participating in the lipid transport involved in lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2023 dataset.
cholesterol storage Gene Set From GO Biological Process Annotations 2023 genes participating in the cholesterol storage biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of lipid storage Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset.
cholesterol transport involved in cholesterol storage Gene Set From GO Biological Process Annotations 2023 genes participating in the cholesterol transport involved in cholesterol storage biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2023 dataset.
decreased mast cell histamine storage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mast cell histamine storage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased mast cell protease storage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mast cell protease storage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Glycogen storage disease type 0 (liver GYS2) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type 0 (liver GYS2) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage disease type 0 (muscle GYS1) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type 0 (muscle GYS1) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage disease type II (GAA) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type II (GAA) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage disease type IV (GBE1) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type IV (GBE1) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage disease type Ia (G6PC) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type Ia (G6PC) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage disease type Ib (SLC37A4) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type Ib (SLC37A4) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage disease type XV (GYG1) Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage disease type XV (GYG1) pathway from the Reactome Pathways 2024 dataset.
Glycogen storage diseases Gene Set From Reactome Pathways 2024 proteins participating in the Glycogen storage diseases pathway from the Reactome Pathways 2024 dataset.
positive regulation of lipid storage Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of lipid storage Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset.
lipid transport involved in lipid storage Gene Set From GO Biological Process Annotations 2025 genes participating in the lipid transport involved in lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2025 dataset.
cholesterol storage Gene Set From GO Biological Process Annotations 2025 genes participating in the cholesterol storage biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of triglyceride storage Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of triglyceride storage biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of triglyceride storage Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of triglyceride storage biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of lipid storage Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset.
cholesterol transport involved in cholesterol storage Gene Set From GO Biological Process Annotations 2025 genes participating in the cholesterol transport involved in cholesterol storage biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of cholesterol storage Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of cholesterol storage biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of triglyceride storage Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of triglyceride storage biological process from the curated GO Biological Process Annotations 2025 dataset.
Lysosomal storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lysosomal storage disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Lipid storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lipid storage disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease VI Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease VI from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease I Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease I from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease V Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease V from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease VII Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease VII from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease IV Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease IV from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease II Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease II from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycogen storage disease III Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycogen storage disease III from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Lysosomal storage disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Lysosomal storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Lipid storage disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Lipid storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Lysosomal storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lysosomal storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lipid storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lipid storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease V Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease V in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease VII Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease VII in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease IXc Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease IXc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease IXa Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease IXa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cholesterol ester storage disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cholesterol ester storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease XV Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease XV in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease III Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease III in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease IV Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease IV in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease Ia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease Ia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease IX Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease IX in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lethal congenital glycogen storage disease of heart Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lethal congenital glycogen storage disease of heart in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease VI Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease VI in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease IXd Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease IXd in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease IXb Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease IXb in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease VIII Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease VIII in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycogen storage disease Ib Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease Ib in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Platelet storage pool deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Platelet storage pool deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Storage root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Storage root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Storage tissue Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Storage tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Proteasome storage granule Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proteasome storage granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Protein storage vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Protein storage vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Storage vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Storage vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
monolayer-surrounded lipid storage body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the monolayer-surrounded lipid storage body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Proteasome storage granule Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proteasome storage granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Protein storage vacuole membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Protein storage vacuole membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Lytic vacuole within protein storage vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Lytic vacuole within protein storage vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cholesteryl ester storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cholesteryl ester storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease IIIa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease IIIb Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to glycogen branching enzyme deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glycogen branching enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to acid maltase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to acid maltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cholestanol storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sialic acid storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sialic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal congenital glycogen storage disease of heart Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal congenital glycogen storage disease of heart phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Phytanic acid storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease IXd Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to phosphoglycerate kinase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease IXa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease IXa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to glucose-6-phosphatase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glucose-6-phosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease IXb Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease IXc Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disorder due to hepatic glycogen synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disorder due to hepatic glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to muscle beta-enolase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle beta-enolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to SLC37A4 mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to SLC37A4 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to muscle and heart glycogen synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle and heart glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Triglyceride storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Triglyceride storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Storage pool disease of platelets Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Storage pool disease of platelets phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycoprotein storage disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycoprotein storage disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
hemolysis of donated blood (cold-storage) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the hemolysis of donated blood (cold-storage) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bethlem myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bethlem myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myofibrillar myopathy, ZASP-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, ZASP-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, centronuclear Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 3, autosomal dominant or recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, reducing body, X-linked, early-onset, severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, centronuclear, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with cores Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Minicore myopathy with external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Minicore myopathy with external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Visceral myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Visceral myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Native American myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Native American myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nonaka myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nonaka myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, tubular aggregate, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, tubular aggregate, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myofibrillar myopathy, filamin C-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, filamin C-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy with lactic acidosis, hereditary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy with lactic acidosis, hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe X-linked myotubular myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with excess of thin myofilaments Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal myopathy Markesbery-Griggs type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, with excess of muscle spindles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary myopathy with early respiratory failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked myopathy with postural muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, compton-north Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked dominant scapuloperoneal myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked dominant scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myofibrillar myopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brody myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brody myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, centronuclear, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, reducing body, X-linked, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miyoshi myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Miyoshi myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy with tubular aggregates Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy with tubular aggregates phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myopathy with fiber type disproportion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYOPATHY, CENTRONUCLEAR, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, 2 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CENTRONUCLEAR, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, 1 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Central Core Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Central Core from the curated CTD Gene-Disease Associations dataset.
Bethlem myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bethlem myopathy from the curated CTD Gene-Disease Associations dataset.
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.
Myopathy, Distal, with Anterior Tibial Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.
Miyoshi myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi myopathy from the curated CTD Gene-Disease Associations dataset.
Welander distal myopathy, Swedish type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, MYOFIBRILLAR, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 1 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, MYOFIBRILLAR, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 4 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, MYOFIBRILLAR, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 6 from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 6 from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 1 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 5 from the curated CTD Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.
Scapuloperoneal Myopathy, X-Linked Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant from the curated CTD Gene-Disease Associations dataset.
Myopathy, Hyaline Body, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Hyaline Body, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, Compton-North Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL MYOPATHY, MYH7-RELATED from the curated CTD Gene-Disease Associations dataset.
Distal myopathy, Nonaka type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Hereditary Myopathy with Early Respiratory Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, SPHEROID BODY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, SPHEROID BODY from the curated CTD Gene-Disease Associations dataset.
Minicore Myopathy with External Ophthalmoplegia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Minicore Myopathy with External Ophthalmoplegia from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, with Excessive Autophagy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, with Excessive Autophagy from the curated CTD Gene-Disease Associations dataset.
Myopathy with Lactic Acidosis, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CENTRONUCLEAR, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 3 from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 4 from the curated CTD Gene-Disease Associations dataset.
Nemaline Myopathy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline Myopathy 2 from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy 3, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Inclusion body myopathy autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion body myopathy autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Brody myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brody myopathy from the curated CTD Gene-Disease Associations dataset.
Nemaline Myopathy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline Myopathy 7 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.
mitochondrial myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease mitochondrial myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
brody myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease brody myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bethlem myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bethlem myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
nemaline myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease nemaline myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
central core myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central core myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital structural myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital structural myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
centronuclear myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease centronuclear myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy of extraocular muscle Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy of extraocular muscle from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease myopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
congenital structural myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central core myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central core myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
brody myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brody myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myopathy of extraocular muscle Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bethlem myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bethlem myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
x-linked myopathy with excessive autophagy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease x-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
nemaline myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nemaline myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adult onset multi/minicore myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease adult onset multi/minicore myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variable myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease variable myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild myotubular myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mild myotubular myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inherited myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease inherited myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mitochondrial myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nemaline myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease nemaline myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy, idiopathic inflammatory Gene Set From GAD Gene-Disease Associations genes associated with the disease myopathy, idiopathic inflammatory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term myopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
myopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease myopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
scapuloperoneal myopathy Gene Set From HPO Gene-Disease Associations genes associated with the scapuloperoneal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myofibrillar myopathy Gene Set From HPO Gene-Disease Associations genes associated with the myofibrillar myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mitochondrial myopathy Gene Set From HPO Gene-Disease Associations genes associated with the mitochondrial myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skeletal myopathy Gene Set From HPO Gene-Disease Associations genes associated with the skeletal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myopathy Gene Set From HPO Gene-Disease Associations genes associated with the myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
minicore (multicore) myopathy Gene Set From HPO Gene-Disease Associations genes associated with the minicore (multicore) myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
nemaline myopathy 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, spheroid body Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, spheroid body phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy with extrapyramidal signs Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy with extrapyramidal signs phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, early-onset, with fatal cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
centronuclear myopathy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the centronuclear myopathy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
native american myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the native american myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, x-linked, with postural muscle atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 1, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 1, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, tubular aggregate Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, tubular aggregate phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 8, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 8, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
brody myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the brody myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, actin, congenital, with cores Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, actin, congenital, with cores phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
?myopathy, congenital, compton-north Gene Set From OMIM Gene-Disease Associations genes associated with the ?myopathy, congenital, compton-north phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy with lactic acidosis, hereditary Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy with lactic acidosis, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 5, amish type Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 5, amish type phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital myopathy with excess of muscle spindles Gene Set From OMIM Gene-Disease Associations genes associated with the congenital myopathy with excess of muscle spindles phenotype from the curated OMIM Gene-Disease Associations dataset.
welander distal myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
bethlem myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the bethlem myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, proximal, with early respiratory muscle involvement Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
laing distal myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?myopathy, tubular aggregate, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?myopathy, tubular aggregate, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal myopathy, x-linked dominant Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal myopathy, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 7, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 7, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
mitochondrial myopathy and sideroblastic anemia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the mitochondrial myopathy and sideroblastic anemia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotubular myopathy, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the myotubular myopathy, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 3, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
minicore myopathy with external ophthalmoplegia Gene Set From OMIM Gene-Disease Associations genes associated with the minicore myopathy with external ophthalmoplegia phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, with anterior tibial onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.
cap myopathy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cap myopathy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cap myopathy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cap myopathy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{centronuclear myopathy, autosomal, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {centronuclear myopathy, autosomal, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 9 Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear phenotype from the curated OMIM Gene-Disease Associations dataset.
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, severe early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy due to cpt ii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
nonaka myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the nonaka myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, tateyama type Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset.
visceral myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the visceral myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, actin, congenital, with excess of thin myofilaments Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 10 Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy due to myoadenylate deaminase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease myopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Inclusion Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Core Myopathy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Core Myopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Centronuclear Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Centronuclear Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Actin-Accumulation Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Actin-Accumulation Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Myotubular Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Myotubular Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Centronuclear Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Structural Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Structural Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intranuclear Rod Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intranuclear Rod Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myofibrillar Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myofibrillar Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nemaline Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nemaline Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonaka Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonaka Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tubular Aggregate Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tubular Aggregate Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vacuolar Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vacuolar Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zebra Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zebra Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miyoshi Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bethlem Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bethlem Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minicore Myopathy With External Ophthalmoplegia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minicore Myopathy With External Ophthalmoplegia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multi-Core Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multi-Core Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Myopathy, X-Linked Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sarcoid Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sarcoid Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcohol Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brody Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brody Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myotubular (Centronuclear) Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotubular (Centronuclear) Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Axial Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Critical Illness Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Critical Illness Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Welander Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy With Focal Depletion Of Mitochondria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, With Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing-Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing-Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Myopathy With Early Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Myopathy With Early Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Native American Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Native American Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngodistal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngodistal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Klhl9-Related Early-Onset Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myotubular Myopathy With Abnormal Genital Development Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotubular Myopathy With Abnormal Genital Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Myopathy 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Myopathy With Abundant Macrophages Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Myopathy With Abundant Macrophages in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inclusion Body Myopathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spheroid Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spheroid Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Myopathy With Lactic Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Myopathy With Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy Type 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Samaritan Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Samaritan Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myopathy With Myasthenic-Like Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myopathy With Myasthenic-Like Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmin Related Myopathy With Mallory Body-Like Inclusions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmin Related Myopathy With Mallory Body-Like Inclusions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy, Tpm2-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy, Tpm2-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy, Tpm3-Related (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy, Tpm3-Related (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
myopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the myopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Nemaline myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Nemaline myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Mitochondrial myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Mitochondrial myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myofibrillar myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myofibrillar myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
GNE myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease GNE myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital structural myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital structural myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Centronuclear myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Centronuclear myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 4A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 4A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myofibrillar myopathy 9 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myofibrillar myopathy 9 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Native American myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Native American myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hyaline body myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyaline body myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal myopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Brody myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Brody myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 1B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Nemaline myopathy 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Nemaline myopathy 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Centronuclear myopathy X-linked Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Centronuclear myopathy X-linked from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Myopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital structural myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
GNE myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease GNE myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy X-linked Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy X-linked in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngodistal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngodistal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fatal infantile hypertonic myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy with rimmed vacuoles Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, benign infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked myopathy with excessive autophagy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bethlem myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bethlem myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy with anterior tibial onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Compton-North congenital myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Compton-North congenital myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Scapuloperoneal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 6 with fiber-type disproportion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 6 with fiber-type disproportion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Brody myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brody myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cylindrical spirals myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cylindrical spirals myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 4A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy with extrapyramidal signs Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy with extrapyramidal signs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 5A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 5A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Native American myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Native American myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngodistal myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngodistal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy of extraocular muscle Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 22A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 22A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tubular aggregate myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tubular aggregate myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 22B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 22B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in F Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in F phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SELENON-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SELENON-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN4A-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN4A-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GNE myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GNE myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe X-linked myotubular myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sarcotubular myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sarcotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inclusion body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TPM3-related core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM3-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nemaline myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nemaline myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital multicore myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital multicore myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RYR1-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RYR1-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYH7-related skeletal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH7-related skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visceral myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visceral myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Desmin-related myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Desmin-related myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bethlem myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bethlem myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Collagen 6-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Collagen 6-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Batten-Turner congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Batten-Turner congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Brody myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Brody myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inborn mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inborn mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Actin accumulation myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Actin accumulation myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy 2b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 2b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy 2c Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 2c phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive scapulohumeroperoneal distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy 10b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 10b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MEGF10-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MEGF10-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYPN-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYPN-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Welander distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal infantile hypertonic myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapuloperoneal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability and myopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability and myopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TTN-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TTN-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in POMG Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in POMG phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bailey-Bloch congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bailey-Bloch congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiminicore myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiminicore myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Miyoshi myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Miyoshi myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in PO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in PO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Compton-North congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Compton-North congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy due to lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion-body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion-body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Polyglucosan body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Polyglucosan body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HNRNPDL-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HNRNPDL-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Axial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Axial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SGCG-related congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SGCG-related congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy-lactic acidosis-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-lactic acidosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CAP-congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CAP-congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ACTA1 gene related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTA1 gene related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy due to calsequestrin and SERCA1 protein overload Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy due to calsequestrin and SERCA1 protein overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital nonprogressive myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nonprogressive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyaline body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyaline body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TPM2-related cap myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM2-related cap myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYH2-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH2-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inclusion body myopathy and brain white matter abnormalities Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy and brain white matter abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital structural myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital structural myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood-onset autosomal recessive myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Skeletal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TPM2-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM2-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic inflammatory myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
COL6A2-related core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the COL6A2-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Finnish upper limb-onset distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SPEG-related congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SPEG-related congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
IDUA-related core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the IDUA-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oculopharyngodistal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oculopharyngodistal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Simvastatin-induced myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Simvastatin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Atorvastatin-induced myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Atorvastatin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Statin-induced myopathy (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Statin-induced myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic inflammatory myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic inflammatory myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Myopathy, myosin storage Gene Set

Myopathy, Myosin Storage Gene Set

myopathy, myosin storage Gene Set

Myosin storage myopathy Gene Set

Neutral lipid storage disease with myopathy Gene Set

Neutral Lipid Storage Disease with Myopathy Gene Set

neutral lipid storage disease with myopathy Gene Set

Neutral Lipid Storage Disease With Myopathy Gene Set

Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene Set

Neutral lipid storage myopathy Gene Set

pkc-catalyzed phosphorylation of inhibitory phosphoprotein of myosin phosphatase Gene Set

muscle myosin complex Gene Set

myosin vii complex Gene Set

striated muscle myosin thick filament Gene Set

myosin ii complex Gene Set

myosin i complex Gene Set

myosin complex Gene Set

unconventional myosin complex Gene Set

myosin filament Gene Set

muscle myosin complex Gene Set

myosin iv complex Gene Set

myosin phosphatase complex Gene Set

myosin vii complex Gene Set

myosin xiv complex Gene Set

myosin viii complex Gene Set

myosin ii complex Gene Set

myosin xi complex Gene Set

myosin vi complex Gene Set

myosin i complex Gene Set

myosin complex Gene Set

myosin xviii complex Gene Set

myosin v complex Gene Set

unconventional myosin complex Gene Set

myosin filament Gene Set

WIP-WASp-actin-myosin-IIa complex Gene Set

Rab27a-melanophilin-myosin-Va complex Gene Set

myosin Gene Set

positive regulation of myosin light chain kinase activity Gene Set

striated muscle myosin thick filament assembly Gene Set

negative regulation of myosin-light-chain-phosphatase activity Gene Set

regulation of myosin-light-chain-phosphatase activity Gene Set

regulation of myosin ii filament organization Gene Set

myosin filament organization Gene Set

actin-myosin filament sliding Gene Set

myosin filament assembly Gene Set

skeletal muscle myosin thick filament assembly Gene Set

regulation of myosin light chain kinase activity Gene Set

muscle myosin complex Gene Set

myosin vii complex Gene Set

myosin ii filament Gene Set

striated muscle myosin thick filament Gene Set

myosin ii complex Gene Set

myosin i complex Gene Set

myosin complex Gene Set

unconventional myosin complex Gene Set

myosin filament Gene Set

myosin ii heavy chain binding Gene Set

myosin light chain binding Gene Set

myosin binding Gene Set

myosin tail binding Gene Set

myosin heavy chain binding Gene Set

myosin v binding Gene Set

myosin phosphatase activity Gene Set

myosin ii binding Gene Set

myosin-light-chain-phosphatase activity Gene Set

myosin phosphatase regulator activity Gene Set

myosin head/neck binding Gene Set

myosin light chain kinase activity Gene Set

myosin vi light chain binding Gene Set

myosin vi binding Gene Set

Myosin, N-terminal, SH3-like Gene Set

Myosin light chain kinase-related Gene Set

Telokin/Myosin light chain kinase Gene Set

Myosin tail Gene Set

Unconventional myosin-XVIIIb Gene Set

Obscurin-myosin light chain kinase Gene Set

Myosin S1 fragment, N-terminal Gene Set

Myosin-like IQ motif-containing domain Gene Set

Myosin head, motor domain Gene Set