# congenital muscular dystrophy-dystroglycanopathy type A2

> congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMT2 on 14q24.3

**Wikidata**: [Q66084936](https://www.wikidata.org/wiki/Q66084936)  
**Source**: https://4ort.xyz/entity/congenital-muscular-dystrophy-dystroglycanopathy-type-a2


## References

1. Disease Ontology
2. [Identifiers.org](https://registry.identifiers.org/registry/doid)