hypertrophic cardiomyopathy 2
MeSH: C566171ORPHA: 155
Overview
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566171Orphanet Code
ORPHA:155hypertrophic cardiomyopathy 2
| MeSH | C566171 |
| Orphanet | ORPHA:155 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO