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Fanconi anemia complementation group F
rareFanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM.
- Identifiers
- MONDO:0011325 OMIM:603467
- Causal genes
- FANCF
- Part of
- Fanconi anemia
- Also known as
- FANCF · Fanconi anaemia complementation group type F · Fanconi anemia complementation group type F · Fanconi anemia, complementation group F · Fanconi Anemia, complementation group type F
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