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Echinobase
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, Fanconi pancytopenia type 4, FANCD2

Echinobase Genes : fancd2


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)