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Summary Literature (1)
DOID:0111097 - Fanconi anemia complementation group J


Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRIP1 gene on chromosome 17q22.

Synonyms: FANCJ

In OMIM:
OMIM:609054 - FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ

In Mondo Disease Ontology:
MONDO:0012187 - Fanconi anemia complementation group j

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : brip1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Fanconi anemia (is_a)