Search Ontology:
Human Disease

hypertrophic cardiomyopathy 2

Term ID
DOID:0110308
Synonyms
  • cardiomyopathy familial hypertrophic 2
  • CMH2
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2). https://www.ncbi.nlm.nih.gov/pubmed/8205619
References
Ontology
Human Disease   ( DOID:0110308 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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