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WormBase Tree Display for DO_term: DOID:0110277

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Name Class

DOID:0110277Nameautosomal recessive limb-girdle muscular dystrophy type 2C
StatusValid
DefinitionAn autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12.
SynonymExactDMDA1
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
ParentIs_aDOID:0110274
DB_infoDatabaseOMIMdisease253700
Attribute_ofGene_by_orthologyWBGene00004790