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Summary Literature (0)
DOID:0111090 - Fanconi anemia complementation group R

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in heterozygous mutation in the RAD51 gene on chromosome 15q15.

Synonyms: FANCR

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014986 - Fanconi anemia complementation group R


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

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