hypertrophic cardiomyopathy 13

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Summary

Literature (0)

DOID:0110319 - hypertrophic cardiomyopathy 13

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.

Synonyms: cardiomyopathy familial hypertrophic 13, CMH13

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tnnc1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013195 - hypertrophic cardiomyopathy 13

MONDO:0013195 - hypertrophic cardiomyopathy 13

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)