# autosomal recessive limb-girdle muscular dystrophy type 2M

> autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31

**Wikidata**: [Q1531338](https://www.wikidata.org/wiki/Q1531338)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-limb-girdle-muscular-dystrophy-type-2m


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000106692/MONDO_0012699)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)