Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2D
Disease ID: disease_node_18905
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| Dbxref | ICD10CM:G71.0, MIM:608099, ORDO:62 |
|---|---|
| Subclassof | DOID_0110274 |
| Data Source | DOID |
| Synonyms | Alpha-sarcoglycanopathy, DMDA2, Duchenne-like autosomal recessive muscular dystrophy type 2, LGMD2D, muscular dystrophy, limb-girdle, type 2D, primary adhalinopathy |
| Doid Label | autosomal recessive limb-girdle muscular dystrophy type 2D |
| Doid Description | An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the alpha-sarcoglycan gene (SGCA) on chromosome 17q. |
| Disease Node Id | disease_node_18905 |
| Doid Id | DOID_0110278 |
| Label | Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2D |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Limb-Girdle Muscular Dystrophy(ID:disease_node_18885) (Disease)