1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the GMPPB gene encoding the beta subunit of GDP-mannose pyrophosphorylase on chromosome 3p21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:440 | neuromuscular disease | A neuropathy that affect the nerves that control the voluntary muscles. |
