OBO ID: DOID:0110326
Term Name: hypertrophic cardiomyopathy 20 Search Ontology:
Synonyms:
  • cardiomyopathy familial hypertrophic 20
  • CMH20
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1. https://www.ncbi.nlm.nih.gov/pubmed/20970104
References:
Ontology: Human Disease   ( DOID:0110326 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 20 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NEXN Cardiomyopathy, hypertrophic, 20 613876
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.