| 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. |
| | Id | 128106003 | | Status | Primitive |
| 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 Orphanet simple map | 166078 |
| 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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