Inclusion Body Myopathy

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Results for "Inclusion Body Myopathy": 1002 gene sets

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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
?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.
?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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Beta-thalassemia, dominant inclusion body type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Beta-thalassemia, dominant inclusion body type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
nuclear inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
inclusion body Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores proteins localized to the inclusion body cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
nuclear inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lewy body-like hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body-like hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Beta Thalassemia, Dominant Inclusion Body Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta Thalassemia, Dominant Inclusion Body Type from the curated CTD Gene-Disease Associations dataset.
Myositis, Inclusion Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myositis, Inclusion Body from the curated CTD Gene-Disease Associations dataset.
inclusion body myositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inclusion body myositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myositis, sporadic inclusion-body Gene Set From GAD Gene-Disease Associations genes associated with the disease myositis, sporadic inclusion-body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
distal myopathies; myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sporadic inclusion body myositis Gene Set From GAD Gene-Disease Associations genes associated with the disease sporadic inclusion body myositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deglutition disorders; muscle weakness; myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease deglutition disorders; muscle weakness; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Inclusion Body Myositides_Muscle tissue_GSE3112 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Inclusion Body Myositides_Muscle tissue_GSE3112 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
positive regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
nuclear inclusion body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nuclear inclusion body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
inclusion body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the inclusion body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Myositis, Inclusion Body Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myositis, Inclusion Body phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
alpha-synuclein inclusion body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the alpha-synuclein inclusion body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thalassemia-beta, dominant inclusion-body Gene Set From OMIM Gene-Disease Associations genes associated with the thalassemia-beta, dominant inclusion-body phenotype from the curated OMIM Gene-Disease Associations dataset.
sporadic inclusion-body myositis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease sporadic inclusion-body myositis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Inclusion Body Myositis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myositis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Inclusion-Body Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Inclusion-Body Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Beta Thalassemia, Dominant Inclusion Body Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Beta Thalassemia, Dominant Inclusion Body Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
negative regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
nuclear inclusion body Gene Set From GO Cellular Component Annotations 2023 proteins localized to the nuclear inclusion body cellular component from the curated GO Cellular Component Annotations 2023 dataset.
alpha-synuclein inclusion body Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the alpha-synuclein inclusion body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Inclusion body myositis Gene Set From WikiPathways Pathways 2024 proteins participating in the Inclusion body myositis pathway from the WikiPathways Pathways 2024 dataset.
Calcium mediated T cell apoptosis involved in inclusion body myositis Gene Set From WikiPathways Pathways 2024 proteins participating in the Calcium mediated T cell apoptosis involved in inclusion body myositis pathway from the WikiPathways Pathways 2024 dataset.
negative regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of inclusion body assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of inclusion body assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
nuclear inclusion body Gene Set From GO Cellular Component Annotations 2025 proteins localized to the nuclear inclusion body cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Inclusion body myositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nuclear inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Inclusion body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Inclusion body Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 proteins localized to the Inclusion body cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
Inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Lewy body-like hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Lewy body-like hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Nuclear inclusion body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 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, 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.
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, 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, 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, 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.
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.
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, 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.
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, 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.
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.
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.
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.
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.
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.
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.
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.
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.
Autosomal dominant hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal 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.
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.
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.
body mass; diabetes, type 2; insulin; glucose; body fat Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; insulin; glucose; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; body fat Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased percent body fat/body weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased percent body fat/body weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal percent body fat/body weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
fibrillary inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the fibrillary inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
skein-like inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the skein-like inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
glial cytoplasmic inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the glial cytoplasmic inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
Microvillus inclusion disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microvillus inclusion disease from the curated CTD Gene-Disease Associations dataset.
inclusion conjunctivitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inclusion conjunctivitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
inclusion Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term inclusion in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
muscle fiber inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neutrophil inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the neutrophil inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle fiber cytoplasmatic inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber cytoplasmatic inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
foam cells with lamellar inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the foam cells with lamellar inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral inclusion bodies Gene Set From HPO Gene-Disease Associations genes associated with the cerebral inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
encephalopathy, familial, with neuroserpin inclusion bodies Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.
microvillus inclusion disease Gene Set From OMIM Gene-Disease Associations genes associated with the microvillus inclusion disease phenotype from the curated OMIM Gene-Disease Associations dataset.
Microvillus Inclusion Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microvillus Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Intranuclear Inclusion Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Intranuclear Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Inclusion Cyst Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Inclusion Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Encephalopathy With Neuroserpin Inclusion Bodies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Encephalopathy With Neuroserpin Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Germinal Inclusion Cyst Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Germinal Inclusion Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Fiber Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Fiber Cytoplasmatic Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Cytoplasmatic Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ubiquitin-Positive Cerebral Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ubiquitin-Positive Cerebral Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leukocyte Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leukocyte Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neutrophil Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neutrophil Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foam Cells With Lamellar Inclusion Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foam Cells With Lamellar Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
glial cytoplasmic inclusion Gene Set From GO Cellular Component Annotations 2023 proteins localized to the glial cytoplasmic inclusion cellular component from the curated GO Cellular Component Annotations 2023 dataset.
nervous system inclusion bodies Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nervous system inclusion bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
glial cytoplasmic inclusion Gene Set From GO Cellular Component Annotations 2025 proteins localized to the glial cytoplasmic inclusion cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Microvillus inclusion disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Microvillus inclusion disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial encephalopathy with neuroserpin inclusion bodies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Microvillus inclusion disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Microvillus inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion conjunctivitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion conjunctivitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal intranuclear inclusion disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal intranuclear inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial encephalopathy with neuroserpin inclusion bodies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glial cytoplasmic inclusion Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Glial cytoplasmic inclusion cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Glial cytoplasmic inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Glial cytoplasmic inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
skein-like inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the skein-like inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Hyaline inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Fibrillary inclusion Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Fibrillary inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Neutrophil inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutrophil inclusion bodies phenotype from the curated ClinVar Gene-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.
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, 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, 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.
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.
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.
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.
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, 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.
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, 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.
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, 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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
mammillary body, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in mammillary body, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
body of caudate nucleus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in body of caudate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
body of caudate nucleus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in body of caudate nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
mammillary body, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in mammillary body, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Nucleus of the trapezoid body Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the trapezoid body relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Mammillary body Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Mammillary body relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
body of caudate Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in body of caudate relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
pontobulbar body Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in pontobulbar body relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
pineal body Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in pineal body relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Lewy body dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lewy body dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
nuclear body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
flemming body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the flemming body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
lamellar body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cytoplasmic mrna processing body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytoplasmic mrna processing body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
epidermal lamellar body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the epidermal lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
dense body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dense body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cajal body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cajal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
alveolar lamellar body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the alveolar lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
lewy body core Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lewy body core cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
alveolar lamellar body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the alveolar lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cell body fiber Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cell body fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
neuronal cell body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal cell body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
chromatoid body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromatoid body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
lamellar body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cleavage body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cleavage body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
neuronal cell body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
xy body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the xy body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
multivesicular body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the multivesicular body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
histone locus body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the histone locus body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cell body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cell body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
ciliary basal body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the ciliary basal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
weibel-palade body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the weibel-palade body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
pml body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pml body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
multivesicular body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the multivesicular body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
pip-body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pip-body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
pi-body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pi-body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
lewy body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lewy body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cell body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
barr body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the barr body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
er body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the er body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
spindle pole body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
nuclear body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
flemming body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the flemming body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lewy body corona Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body corona cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lamellar body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cytoplasmic mrna processing body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytoplasmic mrna processing body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
epidermal lamellar body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the epidermal lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
pml body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pml body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
dense body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dense body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
smooth muscle dense body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the smooth muscle dense body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cortical lewy body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cajal body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cajal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
osmiophilic body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the osmiophilic body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
dense nuclear body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dense nuclear body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
new mitotic spindle pole body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the new mitotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
old mitotic spindle pole body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the old mitotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cell body fiber Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell body fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitotic spindle pole body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
neuronal cell body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the neuronal cell body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chromatoid body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromatoid body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lamellar body membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lamellar body membrane 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.
cleavage body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cleavage body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
meiotic spindle pole body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the meiotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
bacterial-type flagellum basal body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the bacterial-type flagellum basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cell body membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lewy body core Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body core cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
multivesicular body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the multivesicular body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
histone locus body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the histone locus body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cell body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
ciliary basal body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ciliary basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
weibel-palade body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the weibel-palade body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
bunina body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the bunina body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
multivesicular body membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the multivesicular body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cytoplasmic u snrnp body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytoplasmic u snrnp body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
pip-body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pip-body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
ubisch body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ubisch body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
pi-body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pi-body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
protein body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the protein body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lewy body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
classical lewy body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the classical lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
barr body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the barr body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
yb body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the yb body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
laminated body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the laminated body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
complex laminated body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the complex laminated body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
pick body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pick body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
nuclear dicing body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear dicing body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
apoptotic body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the apoptotic body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
etioplast prolamellar body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the etioplast prolamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
xy body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the xy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Heinz Body Anemias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heinz Body Anemias from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 from the curated CTD Gene-Disease Associations dataset.
Granuloma, Foreign-Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Granuloma, Foreign-Body from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 3, Autosomal Dominant Lewy Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 3, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 from the curated CTD Gene-Disease Associations dataset.
Body Weight Changes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Body Weight Changes from the curated CTD Gene-Disease Associations dataset.
Lewy Body Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lewy Body Disease from the curated CTD Gene-Disease Associations dataset.
Body Weight Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Body Weight from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 from the curated CTD Gene-Disease Associations dataset.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 4, Autosomal Dominant Lewy Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 4, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.
Body Composition Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Composition in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Fat Distribution Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Fat Distribution in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Weights and Measures Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Weights and Measures in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Height Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Height in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Weight Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Weight in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Mass Index Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Mass Index in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Weight Changes Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Weight Changes in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
body dysmorphic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease body dysmorphic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
uterine body mixed cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uterine body mixed cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gastric body carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric body carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ciliary body cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ciliary body cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ciliary body disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ciliary body disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carotid body cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carotid body cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
malignant ciliary body melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ciliary body melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lewy body dementia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lewy body dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
higher body mass index Gene Set From GAD Gene-Disease Associations genes associated with the disease higher body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; glucocorticoids Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; glucocorticoids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hypertension; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; coronary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; coronary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass diabetes, type 2 glucose insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass diabetes, type 2 glucose insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; seasonal affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol, ldl; cholesterol, total; insulin; apob Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, ldl; cholesterol, total; insulin; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; left ventricular function; blood pressure; left ventricular structure Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2; insulin; glucose; hba(1c) Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; insulin; glucose; hba(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; leptin Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
larger body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease larger body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass index Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; glucose intolerance; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, type 2; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 2; body fat; lipid metabolism Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; body fat; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weights and measures Gene Set From GAD Gene-Disease Associations genes associated with the disease body weights and measures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; hemoglobin a(1c) Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; hemoglobin a(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; glucose Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hiv infections Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; puberty, delayed Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; puberty, delayed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; triglycerides; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastric body ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease gastric body ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hypertension; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cardiovascular diseases; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cardiovascular diseases; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; lipids; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; height; weight Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; height; weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; body weight Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass index and waist circumference Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass index and waist circumference in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body burden of methylmercury Gene Set From GAD Gene-Disease Associations genes associated with the disease body burden of methylmercury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lower body mass index Gene Set From GAD Gene-Disease Associations genes associated with the disease lower body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body composition changes Gene Set From GAD Gene-Disease Associations genes associated with the disease body composition changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; obesity; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hypertension; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body height Gene Set From GAD Gene-Disease Associations genes associated with the disease body height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; obesity; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; lewy body disease; psychomotor disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; lewy body disease; psychomotor disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes, gestational; gestational diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes, gestational; gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acromegaly; body weight Gene Set From GAD Gene-Disease Associations genes associated with the disease acromegaly; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dietary intake and body composition Gene Set From GAD Gene-Disease Associations genes associated with the disease dietary intake and body composition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; gastrointestinal stromal tumors Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; gastrointestinal stromal tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; familial mediterranean fever; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight changes Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose tolerance; insulin; body fat Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; schizophrenia; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; schizophrenia; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; adiposity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; thinness Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cystic fibrosis; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body composition and muscle strength Gene Set From GAD Gene-Disease Associations genes associated with the disease body composition and muscle strength in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body fat; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body fat; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass (lean) Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass (lean) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; glucose; nervous system activity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; glucose; nervous system activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; muscle testing; igf-i Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; muscle testing; igf-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma lipid levels and body mass index Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma lipid levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2; energy expenditure Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; hypertension; insulin sensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma cholesterol levels and body mass index Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma cholesterol levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body composition Gene Set From GAD Gene-Disease Associations genes associated with the disease body composition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; hypertension; insulin; lipids Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; birth weight; height Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; birth weight; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; obesity; osteoarthritis, knee; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; obesity; osteoarthritis, knee; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; bone density Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; glucose; insulin secretion Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight regulation Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin; body fat; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin; body fat; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass index in women. Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass index in women. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; muscle testing Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; muscle testing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lewy body formation Gene Set From GAD Gene-Disease Associations genes associated with the disease lewy body formation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol, hdl; blood pressure Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
minimum lifetime body mass index Gene Set From GAD Gene-Disease Associations genes associated with the disease minimum lifetime body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; hallucinations; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; hallucinations; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2; glucose tolerance; insulin Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; glucose tolerance; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; body fat; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; body fat; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia in lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia in lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; bulimia; starvation Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; bulimia; starvation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cystic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass (bwt, weight gain, bmi); fertility Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass (bwt, weight gain, bmi); fertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body fat distribution Gene Set From GAD Gene-Disease Associations genes associated with the disease body fat distribution in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lewy body disease; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body fat Gene Set From GAD Gene-Disease Associations genes associated with the disease body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; body weight Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; glucose Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; obesity; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; body weight Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; fatty liver; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; fatty liver; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased body fatness Gene Set From GAD Gene-Disease Associations genes associated with the disease increased body fatness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins Gene Set From GAD Gene-Disease Associations genes associated with the disease increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; puberty, precocious; thinness Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; puberty, precocious; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin; body fat Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; leptin; fat mass Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; leptin; fat mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, type 2; obesity; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 2; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2; glucose; birth weight Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol, hdl; insulin; folate; homocysteine Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; insulin; folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; obesity; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; body weight Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetic polymorphism of cytochrome p450 2a6 and the body status of iron stores Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic polymorphism of cytochrome p450 2a6 and the body status of iron stores in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; spinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; osteoarthritis, knee Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; diabetes, type 2; blood pressure Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; diabetes, type 2; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cardiovascular diseases; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cardiovascular diseases; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; overweight; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; overweight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; diabetes, type 2; hypertension; albuminuria; glycohemoglobin a1 Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; hypertension; albuminuria; glycohemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hypertension; obesity; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; lipodystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin sensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; obesity; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; obesity; glucose Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; obesity; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin sensitivity and body composition Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin sensitivity and body composition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; glucose tolerance; insulin; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; triglycerides; blood pressure Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; triglycerides; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass index, blood pressure and cholesterol Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass index, blood pressure and cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; lipids Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term body in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
body fluid secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the body fluid secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cajal body organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cajal body organization biological process from the curated GO Biological Process Annotations 2015 dataset.
pml body organization Gene Set From GO Biological Process Annotations 2015 genes participating in the pml body organization biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of multivesicular body size Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of multivesicular body size biological process from the curated GO Biological Process Annotations 2015 dataset.
endosome to lysosome transport via multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the endosome to lysosome transport via multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric s-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
multivesicular body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the multivesicular body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
ketone body biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the ketone body biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
ketone body catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the ketone body catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cytoplasmic mrna processing body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cytoplasmic mrna processing body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
establishment of body hair planar orientation Gene Set From GO Biological Process Annotations 2015 genes participating in the establishment of body hair planar orientation biological process from the curated GO Biological Process Annotations 2015 dataset.
comma-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of metanephric s-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of metanephric s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cytoplasmic mrna processing body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cytoplasmic mrna processing body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
establishment of body hair or bristle planar orientation Gene Set From GO Biological Process Annotations 2015 genes participating in the establishment of body hair or bristle planar orientation biological process from the curated GO Biological Process Annotations 2015 dataset.
ketone body metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the ketone body metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
s-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
carotid body glomus cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the carotid body glomus cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
detection of hypoxic conditions in blood by carotid body chemoreceptor signaling Gene Set From GO Biological Process Annotations 2015 genes participating in the detection of hypoxic conditions in blood by carotid body chemoreceptor signaling biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of metanephric comma-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of metanephric comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
ciliary body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the ciliary body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cytoplasmic mrna processing body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the cytoplasmic mrna processing body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
endosome transport via multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the endosome transport via multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
mammillary body development Gene Set From GO Biological Process Annotations 2015 genes participating in the mammillary body development biological process from the curated GO Biological Process Annotations 2015 dataset.
late endosome to vacuole transport via multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the late endosome to vacuole transport via multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
nuclear body organization Gene Set From GO Biological Process Annotations 2015 genes participating in the nuclear body organization biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of metanephric s-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of metanephric s-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of multivesicular body size involved in endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of multivesicular body size involved in endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cytoplasmic mrna processing body assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cytoplasmic mrna processing body assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of metanephric comma-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of metanephric comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
polar body extrusion after meiotic divisions Gene Set From GO Biological Process Annotations 2015 genes participating in the polar body extrusion after meiotic divisions biological process from the curated GO Biological Process Annotations 2015 dataset.
ciliary basal body organization Gene Set From GO Biological Process Annotations 2015 genes participating in the ciliary basal body organization biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric comma-shaped body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric comma-shaped body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
post-embryonic body morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the post-embryonic body morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of body fluid levels Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of body fluid levels biological process from the curated GO Biological Process Annotations 2015 dataset.
multivesicular body organization Gene Set From GO Biological Process Annotations 2015 genes participating in the multivesicular body organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular ketone body metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular ketone body metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
ubiquitin-independent protein catabolic process via the multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the ubiquitin-independent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
multivesicular body, internal vesicle lumen Gene Set From GO Cellular Component Annotations 2015 proteins localized to the multivesicular body, internal vesicle lumen cellular component from the curated GO Cellular Component Annotations 2015 dataset.
nuclear body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nuclear body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
flemming body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the flemming body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
lamellar body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cytoplasmic mrna processing body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cytoplasmic mrna processing body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
multivesicular body, internal vesicle Gene Set From GO Cellular Component Annotations 2015 proteins localized to the multivesicular body, internal vesicle cellular component from the curated GO Cellular Component Annotations 2015 dataset.
epidermal lamellar body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the epidermal lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
dense body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the dense body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cajal body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cajal body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
alveolar lamellar body membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
lewy body core Gene Set From GO Cellular Component Annotations 2015 proteins localized to the lewy body core cellular component from the curated GO Cellular Component Annotations 2015 dataset.
alveolar lamellar body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
neuronal cell body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the neuronal cell body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
chromatoid body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the chromatoid body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
lamellar body membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
neuronal cell body membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the neuronal cell body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
xy body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the xy body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cleavage body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cleavage body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cell body membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cell body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
multivesicular body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the multivesicular body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
histone locus body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the histone locus body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cell body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cell body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
ciliary basal body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the ciliary basal body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
weibel-palade body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the weibel-palade body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
pml body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the pml body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
pip-body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the pip-body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
pi-body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the pi-body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
lewy body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the lewy body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
barr body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the barr body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
multivesicular body membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the multivesicular body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cell body fiber Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cell body fiber cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Body mass (lean) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass (lean) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (body mass index interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder (body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass index Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass index (education interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (education interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bone mineral density (paediatric, total body less head) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bone mineral density (paediatric, total body less head) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Fat body mass Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fat body mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass index and cholesterol (psychopharmacological treatment) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index and cholesterol (psychopharmacological treatment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass index (non-asthmatics) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (non-asthmatics) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass index (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass index (asthmatics) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (asthmatics) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
decreased body weight Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
increased body weight Gene Set From GWASdb SNP-Phenotype Associations genes associated with the increased body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
vertebral body sclerosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the vertebral body sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of body weight Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of body height Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sparse body hair Gene Set From HPO Gene-Disease Associations genes associated with the sparse body hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
heinz body anemia Gene Set From HPO Gene-Disease Associations genes associated with the heinz body anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the ciliary body Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vertebral body sclerosis Gene Set From HPO Gene-Disease Associations genes associated with the vertebral body sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased body weight Gene Set From HPO Gene-Disease Associations genes associated with the decreased body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of body weight Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of subcutaneous fat over entire body except buttocks, hips, and thighs Gene Set From HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat over entire body except buttocks, hips, and thighs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the ciliary body Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of body height Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of body height phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent vertebral body mineralization Gene Set From HPO Gene-Disease Associations genes associated with the absent vertebral body mineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased body weight Gene Set From HPO Gene-Disease Associations genes associated with the increased body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplastic iliac body Gene Set From HPO Gene-Disease Associations genes associated with the hypoplastic iliac body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Lewy Body Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lewy Body Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Carotid Body Tumor Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Carotid Body Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Body Weight Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Body Weight phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Body Image Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Body Image phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Gamma-tubulin complex component/Spindle pole body component Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Gamma-tubulin complex component/Spindle pole body component protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nuclear body protein SP140 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear body protein SP140 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Charged multivesicular body protein 1a Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Charged multivesicular body protein 1a protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Basal body-orientation factor 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Basal body-orientation factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Argininosuccinate synthetase, catalytic/multimerisation domain body Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Argininosuccinate synthetase, catalytic/multimerisation domain body protein domain from the InterPro Predicted Protein Domain Annotations dataset.
nuclear body Gene Set From LOCATE Curated Protein Localization Annotations proteins localized to the nuclear body cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.
increased birth body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased percent body fat Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal body height Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cajal body morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cajal body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal body temperature Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hyoid bone body morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hyoid bone body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ketone body level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased organ/body region tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vitreous body morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vitreous body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body mass index Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lean body mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short vertebral body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal prenatal growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prenatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased organ/body region tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lean body mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal body length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal body length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased body temperature Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal embryonic growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased alveolar lamellar body number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased core body temperature Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased core body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased core body temperature Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased core body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
caudal body truncation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the caudal body truncation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal rostral-caudal body axis extension Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal rostral-caudal body axis extension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal birth body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
opacity of vitreous body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the opacity of vitreous body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal circulating ketone body level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent sternum body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent sternum body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased percent body fat Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal postnatal growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
variable body spotting Gene Set From MPO Gene-Phenotype Associations gene mutations causing the variable body spotting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal organ/body region tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pulmonary neuroendocrine body morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary neuroendocrine body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ventral body wall morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ventral body wall morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent vertebral body Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased total body fat amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased total body fat amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Harmonizome 3.0

Inclusion Body Myopathy Gene Set

Inclusion body myopathy Gene Set

Inclusion body myopathy 2 Gene Set

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

Inclusion Body Myopathy 3, Autosomal Dominant Gene Set

Inclusion body myopathy autosomal recessive Gene Set

inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set

inclusion body myopathy, autosomal recessive Gene Set

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

inclusion body myopathy-3 Gene Set

Inclusion Body Myopathy, Autosomal Dominant Gene Set

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set

Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set

Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set

Hereditary inclusion-body myopathy Gene Set

Inclusion body myopathy and brain white matter abnormalities Gene Set

Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Gene Set

Beta-thalassemia, dominant inclusion body type Gene Set

nuclear inclusion body Gene Set

inclusion body Gene Set

inclusion body Gene Set

nuclear inclusion body Gene Set

inclusion body Gene Set

lewy body-like hyaline inclusion Gene Set

Beta Thalassemia, Dominant Inclusion Body Type Gene Set

Myositis, Inclusion Body Gene Set

inclusion body myositis Gene Set

myositis, sporadic inclusion-body Gene Set

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

distal myopathies; myositis, inclusion body Gene Set

sporadic inclusion body myositis Gene Set

myositis, inclusion body Gene Set

deglutition disorders; muscle weakness; myositis, inclusion body Gene Set

Inclusion Body Myositides_Muscle tissue_GSE3112 Gene Set

positive regulation of inclusion body assembly Gene Set

inclusion body assembly Gene Set

negative regulation of inclusion body assembly Gene Set

regulation of inclusion body assembly Gene Set

nuclear inclusion body Gene Set

inclusion body Gene Set

Myositis, Inclusion Body Gene Set

alpha-synuclein inclusion body Gene Set

thalassemia-beta, dominant inclusion-body Gene Set

sporadic inclusion-body myositis Gene Set

Inclusion Body Myositis (Disorder) Gene Set

Atypical Inclusion-Body Disease Gene Set

Beta Thalassemia, Dominant Inclusion Body Type Gene Set

negative regulation of inclusion body assembly Gene Set

regulation of inclusion body assembly Gene Set

inclusion body assembly Gene Set

positive regulation of inclusion body assembly Gene Set

nuclear inclusion body Gene Set

alpha-synuclein inclusion body Gene Set

Inclusion body myositis Gene Set

Calcium mediated T cell apoptosis involved in inclusion body myositis Gene Set

negative regulation of inclusion body assembly Gene Set

regulation of inclusion body assembly Gene Set

inclusion body assembly Gene Set

positive regulation of inclusion body assembly Gene Set

nuclear inclusion body Gene Set

Inclusion body myositis Gene Set

Nuclear inclusion body Gene Set

Inclusion body Gene Set

Inclusion body Gene Set

Inclusion body Gene Set

Lewy body-like hyaline inclusion Gene Set

Nuclear inclusion body Gene Set

Myopathy, reducing body, X-linked, early-onset, severe Gene Set

Myopathy, reducing body, X-linked, childhood-onset Gene Set

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set

Myopathy, Hyaline Body, Autosomal Recessive Gene Set

MYOPATHY, SPHEROID BODY Gene Set

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set