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Summary Literature (0)
DOID:0111093 - Fanconi anemia complementation group Q

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the ERCC4 gene on chromosome 16p13.

Synonyms: FANCQ

Xenbase Genes : ercc4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014108 - Fanconi anemia complementation group Q


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)