hypertrophic cardiomyopathy 9
MeSH: C566044ORPHA: 155
Overview
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TTN gene on chromosome 2q31
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566044Orphanet Code
ORPHA:155hypertrophic cardiomyopathy 9
| MeSH | C566044 |
| Orphanet | ORPHA:155 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO