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DOID:0111086 - Fanconi anemia complementation group G
Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13.
Synonyms: FANCG,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0013565 - Fanconi anemia complementation group G |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Fanconi anemia (is_a),
monogenic disease (is_a)