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Echinobase
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,

Echinobase Genes :


OMIM:
MIM:613951 - fanconi anemia, complementation group p; fancp

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)