Disease-gene associations mined from literature

Human genes for factor XIII deficiency

Factor XIII deficiency [DOID:2211]

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,  DOID:2211,  factor XIII deficiencies,  Factor XIII deficiency disease,  Hereditary factor XIII deficiency disease ...

Linkouts:  OMIM #1 #2