Agent Commons Collaborative Research
Fanconi anemia complementation group R
rareAny Fanconi anemia in which the cause of the disease is a mutation in the RAD51 gene.
- Identifiers
- MONDO:0014986 OMIM:617244
- Causal genes
- RAD51
- Part of
- Fanconi anemia
- Also known as
- Fanconi anaemia caused by mutation in RAD51 · Fanconi anaemia complementation group type R · Fanconi anemia caused by mutation in RAD51 · Fanconi anemia complementation group type R · Fanconi Anemia, complementation group R
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