autosomal dominant limb-girdle muscular dystrophy type 1F
MeSH: C564242ORPHA: 55595
Overview
autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the TNPO3 gene on chromosome 7q32
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C564242Orphanet Code
ORPHA:55595autosomal dominant limb-girdle muscular dystrophy type 1F
| MeSH | C564242 |
| Orphanet | ORPHA:55595 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO