ziekte van von Willebrand type 1 (aandoening)
ziekte van von Willebrand type 1
Hereditary von Willebrand disease type 1
von Willebrand disease type 1
A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner.
Has interpretationafwijkend
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermZiekte van Willebrand
SNOMED CT to Orphanet simple map166078
SNOMED CT to ICD-10 extended map
AdviceALWAYS D68.0
CorrelationSNOMED CT source code to target map code correlation not specified