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DOID:0110326 - hypertrophic cardiomyopathy 20
Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
Synonyms: CMH20, cardiomyopathy familial hypertrophic 20,
Xenbase Genes : nexn
MONDO:0013477 - hypertrophic cardiomyopathy 20 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee