Search Ontology:
Human Disease

hypertrophic cardiomyopathy 25

Term ID
DOID:0110328
Synonyms
  • cardiomyopathy familial hypertrophic 25
  • CMH25
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12. https://www.ncbi.nlm.nih.gov/pubmed/15582318
References
Ontology
Human Disease   ( DOID:0110328 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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