OBO ID: DOID:0110308
Term Name: hypertrophic cardiomyopathy 2 Search Ontology:
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 hypertrophic cardiomyopathy 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TNNT2 Cardiomyopathy, hypertrophic, 2 115195
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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