Autosomal dominant hereditary disorder
Hereditary hypoplasminogenemia
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Autosomal dominant deficiency of plasminogen (disorder)
Autosomal dominant deficiency of plasminogen
Autosomal dominant deficiency of profibrinolysin
autosomaal dominante plasminogeendeficiëntie
autosomaal dominante deficiëntie van profibrinolysine
Id95842004
StatusPrimitive
Has interpretationAbnormal
InterpretsHemostatic function
ICD-10 complex map reference set
TargetD68.2
RuleTRUE
AdviceALWAYS D68.2 | MAPPED FOLLOWING WHO GUIDANCE
CorrelationSNOMED CT source code to target map code correlation not specified