# autosomal dominant limb-girdle muscular dystrophy type 1F

> autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the TNPO3 gene on chromosome 7q32

**Wikidata**: [Q1531328](https://www.wikidata.org/wiki/Q1531328)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-limb-girdle-muscular-dystrophy-type-1f


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.
5. Next-generation sequencing identifies transportin 3 as the causative gene for LGMD1F
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)