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Metadata
ID	DOID:0110326
Name	hypertrophic cardiomyopathy 20
Definition	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1. https://www.ncbi.nlm.nih.gov/pubmed/20970104
Xrefs	OMIM:613876
Synonyms	cardiomyopathy familial hypertrophic 20 [EXACT] CMH20 [EXACT]
Parent Relationships	is_a familial hypertrophic cardiomyopathy