myostatin-related muscle hypertrophy
MeSH: C536106ORPHA: 275534
Overview
muscle tissue disease characterized by increased muscle bulk and strength that has material basis in homozygous mutation in the MSTN gene on chromosome 2q32.2
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C536106Orphanet Code
ORPHA:275534myostatin-related muscle hypertrophy
| MeSH | C536106 |
| Orphanet | ORPHA:275534 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO