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MIRAGE
autosomal recessive limb-girdle muscular dystrophy type 2C
Summary
- Synonym
-
- 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
- Definition
- An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12.
- Super Class
- autosomal recessive limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110277
- Mondo Disease Ontology
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q13326 | Gamma-sarcoglycan |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P82348 | Gamma-sarcoglycan |
