Fanconi anemia complementation group T

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the UBE2T gene.

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 type T, FANCT, UBE2T Fanconi anaemia, UBE2T Fanconi anemia — per MONDO

Also identified as

• DOID 0111081 per MONDO
• OMIM 616435 per MONDO
• UMLS C4084840 per MONDO