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Fanconi anemia complementation group T
rareAny Fanconi anemia in which the cause of the disease is a mutation in the UBE2T gene.
- Identifiers
- MONDO:0014638 OMIM:616435
- Causal genes
- UBE2T
- Part of
- Fanconi anemia
- Also known as
- Fanconi anaemia caused by mutation in UBE2T · Fanconi anaemia complementation group type T · Fanconi anemia caused by mutation in UBE2T · Fanconi anemia complementation group type T · Fanconi anemia, complementation group T
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