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Fanconi anemia complementation group V
rareAny Fanconi anemia in which the cause of the disease is a mutation in the MAD2L2 gene.
- Identifiers
- MONDO:0014985 OMIM:617243
- Causal genes
- MAD2L2
- Part of
- Fanconi anemia
- Also known as
- Fanconi anaemia caused by mutation in MAD2L2 · Fanconi anaemia complementation group type V · Fanconi anemia caused by mutation in MAD2L2 · Fanconi anemia complementation group type V · Fanconi Anemia, complementation group type V
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