Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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: Factor XIII deficiency disease, Factor XIII deficiency disease (disorder), Hereditary factor XIII deficiency disease, Hereditary factor XIII deficiency disease (disorder), deficiency, Laki-Lorand factor

Xenbase Genes : f13a1, f13b, f13bl

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018029 - congenital factor XIII deficiency

OMIM:
OMIM:613225 - FACTOR XIII, A SUBUNIT, DEFICIENCY OF
OMIM:613235 - FACTOR XIII, B SUBUNIT, DEFICIENCY OF

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

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