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Fanconi anemia complementation group T(FANCT)

MedGen UID:
896157
Concept ID:
C4084840
Disease or Syndrome
Synonyms: FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT
 
UBE2T (1q32.1)
 
Monarch Initiative: MONDO:0014638
OMIM®: 616435
Authors:

Additional description

From OMIM
Fanconi anemia is characterized by genomic instability, increased susceptibility to cancer development, and bone marrow failure associated with various developmental abnormalities, such as radial ray anomalies or short stature (summary by Hira et al., 2015). For a discussion of genetic heterogeneity of Fanconi anemia, see FANCA (227650).  http://www.omim.org/entry/616435

Clinical features

From HPO

Supplemental Content

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