Autosomal dominant hereditary disorder
von Willebrand disease type 2
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Hereditary von Willebrand disease type 2B (disorder)
Hereditary von Willebrand disease type 2B
hereditaire ziekte van von Willebrand type 2B
Id359717002
StatusPrimitive
Has interpretationAbnormal
InterpretsHemostatic function
ICD-10 complex map reference set
TargetD68.0
RuleTRUE
AdviceALWAYS D68.0
CorrelationSNOMED CT source code to target map code correlation not specified