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Disease Ontology Browser
factor XIII deficiency (DOID:2211)
Alliance: disease page
Synonyms: deficiency, Laki-Lorand factor; Factor XIII deficiency disease; Hereditary factor XIII deficiency disease
Alt IDs: OMIM:613225, OMIM:613235, MESH:D005177, NCI:C98941, UMLS_CUI:C0015530
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.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory