Alpha-2-antiplasmin deficiency
Autosomal recessive hereditary disorder
Congenital disease
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Congenital alpha-2-antiplasmin deficiency (disorder)
Congenital alpha-2-antiplasmin deficiency
Congenital alpha2-antiplasmin deficiency
A rare hemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes. Inherited in an autosomal recessive manner.
congenitale alfa-2-antiplasminedeficiëntie
aangeboren alfa-2-antiplasminedeficiëntie
Id716746003
StatusPrimitive
OccurrenceCongenital
Has interpretationAbnormal
InterpretsHemostatic function
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetD68.8
RuleTRUE
AdviceALWAYS D68.8
CorrelationSNOMED CT source code to target map code correlation not specified