OBO ID: DOID:0110315
Term Name: hypertrophic cardiomyopathy 9 Search Ontology:
Synonyms:
  • cardiomyopathy, familial hypertrophic, 9
  • CMH9
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TTN gene on chromosome 2q31. https://www.ncbi.nlm.nih.gov/pubmed/10462489
References:
Ontology: Human Disease   ( DOID:0110315 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TTN Cardiomyopathy, familial hypertrophic, 9 613765
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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