Fanconi Anemia, Complementation Group D2, also known as fanconi anemia complementation group d2, is related to ataxia-telangiectasia and fanconi anemia, complementation group b, and has symptoms including anemic pallor An important gene associated with Fanconi Anemia, Complementation Group D2 is FANCD2 (FA Complementation Group D2), and among its related pathways/superpathways are Homology Directed Repair and DNA Damage. The drugs Talazoparib and Niraparib have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and bone, and related phenotypes are microcephaly and bone marrow hypocellularity