autosomal dominant limb-girdle muscular dystrophy type 1G
MeSH: C563794ORPHA: 55596
Overview
autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the HNRNPDL gene on chromosome 4q21
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C563794Orphanet Code
ORPHA:55596autosomal dominant limb-girdle muscular dystrophy type 1G
| MeSH | C563794 |
| Orphanet | ORPHA:55596 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO