Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0111083 - Fanconi anemia complementation group D2

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25.

Synonyms: FA4, FAD2, FANCD2, Fanconi pancytopenia type 4

Xenbase Genes : fancd2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009214 - Fanconi anemia complementation group D2

MIM:
MIM:227646 - FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), Fanconi anemia (is_a)