has material basis in germline mutation in FANCD2 Fanconi anemia complementation group D2 https://www.malacards.org/card/fanconi_anemia_complementation_group_d2 Fanconi anemia, complementation group D2 OMIM:227646 GARD:0015169 MEDGEN:463627 NCIT:C125706 Fanconi anemia complementation group D2 DOID:0111083 FANCD2 Fanconi anemia caused by mutations of the FANCD2 gene. This gene is involved in the repair of DNA double-strand breaks, both by homologous recombination and single-strand annealing. Fanconi pancytopenia, type 4 FAD2 Fad2 FA4 UMLS:C3160738 MONDO:0009214 Fanconi Anemia, complementation group D Fanconi anemia