# MEND syndrome

> human disease

**Wikidata**: [Q55782508](https://www.wikidata.org/wiki/Q55782508)  
**Source**: https://4ort.xyz/entity/mend-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Molecular, biochemical, and phenotypic analysis of a hemizygous male with a severe atypical phenotype for X-linked dominant Conradi-Hunermann-Happle syndrome and a mutation in EBP.
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000147155/MONDO_0010498)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)