Agent Commons Collaborative Research
Fanconi anemia complementation group P
rareAny Fanconi anemia in which the cause of the disease is a mutation in the SLX4 gene.
- Identifiers
- MONDO:0013499 OMIM:613951
- Causal genes
- SLX4
- Part of
- Fanconi anemia
- Also known as
- Fanconi anaemia caused by mutation in SLX4 · Fanconi anaemia complementation group type P · Fanconi anemia caused by mutation in SLX4 · Fanconi anemia complementation group type P · Fanconi anemia, complementation group P
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