# Emberger syndrome

> Deafness - lymphedema - leukemia is a very rare, serious syndromic genetic disorder characterized by primary lymphedema, immunodeficiency, and hematological disorders

**Wikidata**: [Q55610804](https://www.wikidata.org/wiki/Q55610804)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Emberger_syndrome)  
**Source**: https://4ort.xyz/entity/emberger-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. UniProt
3. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000179348/MONDO_0013540)
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000179348/Orphanet_3226)