OBO ID: DOID:0110327
Term Name: hypertrophic cardiomyopathy 26 Search Ontology:
Synonyms:
  • cardiomyopathy familial hypertrophic 26
  • CMH26
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32. https://www.ncbi.nlm.nih.gov/pubmed/25351925
References:
Ontology: Human Disease   ( DOID:0110327 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 26 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FLNC Arrhythmogenic right ventricular dysplasia, familial 617047
Cardiomyopathy, familial restrictive 5 617047
Cardiomyopathy, familial hypertrophic, 26 617047
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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