WormBase Tree Display for DO_term: DOID:0110277
expand all nodes | collapse all nodes | view schema
DOID:0110277 | Name | autosomal recessive limb-girdle muscular dystrophy type 2C | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12. | ||||
Synonym | Exact | DMDA1 | |||
LGMD2C | |||||
Maghrebian myopathy | |||||
SCARMD | |||||
autosomal recessive Duchenne-like muscular dystrophy type 1 | |||||
deficiency of sarcoglycan gamma | |||||
gamma-sarcoglycanopathy | |||||
limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency | |||||
muscular dystrophy, limb-girdle, type 2C | |||||
severe childhood autosomal recessive muscular dystrophy North African type | |||||
Parent | Is_a | DOID:0110274 | |||
DB_info | Database | OMIM | disease | 253700 | |
Attribute_of | Gene_by_orthology | WBGene00004790 |