# Charcot-Marie-Tooth disease dominant intermediate D

> Charcot-Marie-Tooth disease intermediate type that has material basis in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23

**Wikidata**: [Q27677663](https://www.wikidata.org/wiki/Q27677663)  
**Source**: https://4ort.xyz/entity/charcot-marie-tooth-disease-dominant-intermediate-d


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000158887/MONDO_0011909)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000158887/Orphanet_100046)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)