Fanconi anemia complementation group U

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the XRCC2 gene.

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, Fanconi Anemia, complementation group U, FANCU, XRCC2 Fanconi anaemia, XRCC2 Fanconi anemia — per MONDO

Also identified as

• DOID 0111085 per MONDO
• OMIM 617247 per MONDO
• UMLS C4310651 per MONDO