hypertrophic cardiomyopathy 4 (Q27674921)
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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
- CMH4
- cardiomyopathy, familial hypertrophic, 4
- familial hypertrophic cardiomyopathy type 4
- Cardiomyopathy, Familial Hypertrophic, 4, Susceptibility to
- Cardiomyopathy, Familial Hypertrophic, type 4
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4
- hypertrophic cardiomyopathy type 4
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 4 |
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 |
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Statements
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C133725
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C133725
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Identifiers
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