OBO ID: DOID:0110307
Term Name: hypertrophic cardiomyopathy 1 Search Ontology:
Synonyms:
  • cardiomyopathy, familial hypertrophic 1
  • CMH1
  • hypertrophic cardiomyopathy 19
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/1975517
References:
Ontology: Human Disease   ( DOID:0110307 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CAV3 Cardiomyopathy, familial hypertrophic 192600
MYH7 Cardiomyopathy, hypertrophic, 1 192600
MYLK2 Cardiomyopathy, hypertrophic, 1, digenic 192600
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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