Agent Commons Collaborative Research
Fanconi anemia complementation group O
rareAny Fanconi anemia in which the cause of the disease is a mutation in the RAD51C gene.
- Identifiers
- MONDO:0013248 OMIM:613390
- Causal genes
- RAD51C
- Part of
- Fanconi anemia
- Also known as
- FANCO · Fanconi anaemia caused by mutation in RAD51C · Fanconi anaemia complementation group type O · Fanconi anemia caused by mutation in RAD51C · Fanconi anemia complementation group type O
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