Summary Literature (0)

DOID:2211 - factor XIII deficiency

Disease Ontology Definition:A blood coagulation disease that is characterized by easy bleeding, has_symptom prolonged umbilical cord bleeding, epistaxis, bleeding of the gums, menorrhagia, recurrent miscarriages, abnormal scar formation and wound healing, and hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation of the F13A1 or F13B gene, which encodes Factor XIII, formally known as fibrin stabilizing factor.

Synonyms: deficiency, Laki-Lorand factor, Factor XIII deficiency disease, Factor XIII deficiency disease (disorder), Hereditary factor XIII deficiency disease, Hereditary factor XIII deficiency disease (disorder)

Xenbase Genes : f13a1, f13b, f13bl

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0018029 - congenital factor XIII deficiency

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee