(Q27674921)
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
- 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
Statements
1 reference
4 references
C133725
0 references
C133725
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference