Search Ontology:
Human Disease

hypertrophic cardiomyopathy 7

Term ID
DOID:0110313
Synonyms
  • cardiomyopathy, familial hypertrophic 7
  • CMH7
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4. https://www.ncbi.nlm.nih.gov/pubmed/9241277
References
Ontology
Human Disease   ( DOID:0110313 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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