hypertrophic cardiomyopathy 3
MeSH: C566170ORPHA: 155
Overview
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566170Orphanet Code
ORPHA:155hypertrophic cardiomyopathy 3
| MeSH | C566170 |
| Orphanet | ORPHA:155 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO