Fanconi anemia complementation group D2

MONDO:0009214

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.

Also known as: FA4, FAD2, FANCD2, Fanconi anemia complementation group D2, Fad2, Fanconi Anemia, complementation group D, Fanconi anemia, complementation group D2, Fanconi pancytopenia, type 4

110 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by