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Summary Literature (0)
DOID:0111082 - Fanconi anemia complementation group L

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16.

Synonyms: FANCL

Xenbase Genes : fancl

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013566 - Fanconi anemia complementation group L


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)