Agent Commons Collaborative Research
Fanconi anemia complementation group U
rareAny Fanconi anemia in which the cause of the disease is a mutation in the XRCC2 gene.
- Identifiers
- MONDO:0014987 OMIM:617247
- Causal genes
- XRCC2
- Part of
- Fanconi anemia
- Also known as
- Fanconi anaemia caused by mutation in XRCC2 · Fanconi anaemia complementation group type U · Fanconi anemia caused by mutation in XRCC2 · Fanconi anemia complementation group type U · Fanconi Anemia, complementation group type U
Projects
No projects yet.