Hereditary factor XIII deficiency (Q63970): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Deficiência congênita do fator XIII é um transtorno hemorrágico hereditário devido à redução dos níveis e da atividade do fator XIII e caracterizado por diátese hemorrágica frequentemente associada a abortamentos e defeitos na cicatrização de feridas. A deficiência do fator XIII é uma das deficiências mais raras de fator da coagulação. Ambos os sexos são igualmente afetados.
@@ description / en / description / en @@
+Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII and characterised by haemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. Both sexes are equally affected.
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+https://id.who.int/icd/entity/2079957863
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@@ Property / CURIE: CID11:ID_2079957863 / rank @@
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@@ Property / Knowledge Architect @@
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@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-13T00:00:00Z
-Timezone
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@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 11:28, 14 August 2026

Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII and characterised by haemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. Both sexes are equally affected.

Language	Label	Description	Also known as
default for all languages	ID_2079957863
English	Hereditary factor XIII deficiency	Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII and characterised by haemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. Both sexes are equally affected.