Search Ontology:
Human Disease

factor XIII deficiency

Term ID
DOID:2211
Synonyms
  • deficiency, Laki-Lorand factor
  • Factor XIII deficiency disease
  • Hereditary factor XIII deficiency disease
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. (3)
References
Ontology
Human Disease   ( DOID:2211 )
Relationships
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Genes Involved
Zebrafish Models