Search Ontology:
Human Disease

hypertrophic cardiomyopathy 12

Term ID
DOID:0110318
Synonyms
  • cardiomyopathy familial hypertrophic 12
  • CMH12
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/12642359
References
Ontology
Human Disease   ( DOID:0110318 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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