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Summary Literature (0)
DOID:0111092 - Fanconi anemia complementation group P

Disease Ontology Definition:A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3.

Synonyms: FANCP

Xenbase Genes : slx4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013499 - Fanconi anemia complementation group P

MIM:
MIM:613951 - FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP

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)