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Fanconi anemia complementation group B
rareFanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B.
- Identifiers
- MONDO:0010351 OMIM:300514
- Causal genes
- FANCB
- Part of
- Fanconi anemia
- Also known as
- FA2 · FACB · FANCB · Fanconi anaemia complementation group type B · Fanconi anemia complementation group type B
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