Search Ontology:
Human Disease

hypertrophic cardiomyopathy 20

Term ID
DOID:0110326
Synonyms
  • cardiomyopathy familial hypertrophic 20
  • CMH20
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
References
Ontology
Human Disease   ( DOID:0110326 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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