# SLC39A8-CDG

> human disease

**Wikidata**: [Q55784972](https://www.wikidata.org/wiki/Q55784972)  
**Source**: https://4ort.xyz/entity/slc39a8-cdg


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000138821/MONDO_0014746)