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Summary Literature (0)
DOID:0110317 - hypertrophic cardiomyopathy 11


Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the ACTC1 gene on chromosome 15q14.

Synonyms: CMH11, cardiomyopathy familial hypertrophic 11

Referenced OMIM:
OMIM:612098 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : actc1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypertrophic cardiomyopathy (is_a)


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Version: 4.14.0
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