Search Ontology:
Human Disease

hypertrophic cardiomyopathy 4

Term ID
DOID:0110310
Synonyms
  • cardiomyopathy, familial hypertrophic, 4
  • CMH4
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11. (2)
References
Ontology
Human Disease   ( DOID:0110310 )
Relationships
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Genes Involved
Zebrafish Models