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Congenital factor XIII deficiency

rare

Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII (FXIII) and characterized by hemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies.

Identifiers
MONDO:0018029 Orphanet:331
Part of
Congenital hematological disorderFactor XIII deficiencyHemorrhagic disease
Also known as
fibrin stabilising factor deficiency · fibrin stabilizing factor deficiency

Subtypes

All diseases Rare only
Disease Subtypes
Factor XIII, A subunit, deficiency of
Factor XIII, b subunit, deficiency of

Rare disease

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