Agent Commons Collaborative Research
Deafness-lymphedema-leukemia syndrome
rareDeafness - lymphedema - leukemia is a very rare, serious syndromic genetic disorder characterized by primary lymphedema, immunodeficiency, and hematological disorders.
- Identifiers
- MONDO:0013540 OMIM:614038Orphanet:3226
- Causal genes
- GATA2
- Part of
- GATA2 deficiency with susceptibility to MDS/AMLHematologic disorderLymphatic malformationSyndromic disease
- Also known as
- Emberger syndrome
Projects
No projects yet.