Search Ontology:
Human Disease

hypertrophic cardiomyopathy 1

Term ID
DOID:0110307
Synonyms
  • cardiomyopathy, familial hypertrophic 1
  • CMH1
  • hypertrophic cardiomyopathy 19
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/1975517
References
Ontology
Human Disease   ( DOID:0110307 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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