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Fanconi anemia complementation group I

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Fanconi anemia caused by mutations in the FANCI gene, encoding Fanconi anemia group I protein.
Uniprot Description A disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. It is associated with cardiac, renal and limb malformations, dermal pigmentary changes, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair.
Mondo Term and Equivalent IDs
MONDO:0012186:  Fanconi anemia complementation group I
MESH:C563802: 
NCIT:C129026: 
UMLS:C1836861: