# Charcot-Marie-Tooth disease type 2A2

> Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the MFN2 gene on chromosome 1p36.2

**Wikidata**: [Q27164461](https://www.wikidata.org/wiki/Q27164461)  
**Source**: https://4ort.xyz/entity/charcot-marie-tooth-disease-type-2a2


## References

1. Disease Ontology
2. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000116688/Orphanet_99947)
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. UMLS 2023