# autosomal recessive limb-girdle muscular dystrophy type 2D

> autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the alpha-sarcoglycan gene (SGCA; 600119) on chromosome 17q

**Wikidata**: [Q24960548](https://www.wikidata.org/wiki/Q24960548)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-limb-girdle-muscular-dystrophy-type-2d


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000108823/MONDO_0011968)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)