Autosomal dominant hereditary disorder
von Willebrand disease type 2
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Hereditary von Willebrand disease type 2M (disorder)
Hereditary von Willebrand disease type 2M
hereditaire ziekte van von Willebrand type 2M
Id359725000
StatusPrimitive
Has interpretationAbnormal
InterpretsHemostatic function
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetD68.0
RuleTRUE
AdviceALWAYS D68.0
CorrelationSNOMED CT source code to target map code correlation not specified