|
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:0013566 - Fanconi anemia complementation group L |
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)