Search Ontology:
Human Disease
hypertrophic cardiomyopathy 4
- Term ID
- DOID:0110310
- Synonyms
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models