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Summary Literature (0)
DOID:2231 - factor XII deficiency

Disease Ontology Definition:A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33.

Synonyms: deficiency, Hageman, Factor XII deficiency disease, Hageman Factor deficiency

Xenbase Genes : f12

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009315 - congenital factor XII deficiency


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal genetic disease (is_a), autosomal recessive disease (is_a), blood coagulation disease (is_a)