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DOID:0110313 - hypertrophic cardiomyopathy 7
Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
Synonyms: CMH7, cardiomyopathy, familial hypertrophic 7,
Xenbase Genes : tnni3
MONDO:0013369 - hypertrophic cardiomyopathy 7 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypertrophic cardiomyopathy (is_a)