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OBO ID: DOID:0111427
Term Name: restrictive cardiomyopathy 3 Search Ontology:
Synonyms:
  • familial restrictive cardiomyopathy 3
  • RCM3
Definition: A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in TNNT2 on chromosome 1q32.1. https://www.ncbi.nlm.nih.gov/pubmed/16651346
References:
Ontology: Human Disease   (DOID:0111427)
OTHER restrictive cardiomyopathy 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TNNT2 Cardiomyopathy, familial restrictive, 3 612422
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None