Search Ontology:
Human Disease

hypertrophic cardiomyopathy 8

Term ID
DOID:0110314
Synonyms
  • cardiomyopathy hypertrophic mid-left ventricular chamber type 1
  • cardiomyopathy, familial hypertrophic, 8
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene. https://www.ncbi.nlm.nih.gov/pubmed/8673105
References
Ontology
Human Disease   ( DOID:0110314 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models