# autosomal dominant limb-girdle muscular dystrophy type 1G

> autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the HNRNPDL gene on chromosome 4q21

**Wikidata**: [Q1531329](https://www.wikidata.org/wiki/Q1531329)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-limb-girdle-muscular-dystrophy-type-1g


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)