Search Ontology:
Human Disease

hypertrophic cardiomyopathy 3

Term ID
DOID:0110309
Synonyms
  • cardiomyopathy familial hypertrophic 3
  • CMH3
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/8205619
References
Ontology
Human Disease   ( DOID:0110309 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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