| ziekte van von Willebrand (aandoening) | | ziekte van von Willebrand | | ziekte van Von Willebrand | | Ziekte met een verhoogde kans op bloedingen door een tekort aan een bepaald stollingseiwit in het bloed (de von willebrandfactor). | | von Willebrand disorder | | vWD - von Willebrand's disease
von Willebrand's disease
Factor VIII deficiency with vascular defect
von Willebrand disease
von Willebrand disease, platelet type
von Willebrand-Jurgens disease
Constitutional thrombopathy
Vascular hemophilia
Angiohemophilia
Pseudohemophilia type B
| | Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. |
| | Id | 128105004 | | Status | Primitive |
| General Practice / Family Practice reference set |
| International Patient Summary |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | D68.0 | | Term | Ziekte van Willebrand |
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| SNOMED CT to MedDRA simple map | 10047715 |
| SNOMED CT to ICD-10 extended map | | Target | D68.0 | | Rule | TRUE | | Advice | ALWAYS D68.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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