OBO ID: DOID:0110319
Term Name: hypertrophic cardiomyopathy 13 Search Ontology:
Synonyms:
  • cardiomyopathy familial hypertrophic 13
  • CMH13
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/11385718
References:
Ontology: Human Disease   ( DOID:0110319 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 13 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TNNC1 Cardiomyopathy, hypertrophic, 13 613243
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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