# X-linked distal spinal muscular atrophy type 3

> human disease

**Wikidata**: [Q55345735](https://www.wikidata.org/wiki/Q55345735)  
**Source**: https://4ort.xyz/entity/x-linked-distal-spinal-muscular-atrophy-type-3


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000165240/MONDO_0010338)