autosomal recessive limb-girdle muscular dystrophy type 2G
MeSH: C566599ORPHA: 34514
Overview
autosomal recessive limb-girdle muscular dystrophy that has material basis in mutation in the gene encoding telethonin (TCAP)
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566599Orphanet Code
ORPHA:34514autosomal recessive limb-girdle muscular dystrophy type 2G
| MeSH | C566599 |
| Orphanet | ORPHA:34514 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO