| rabdomyosarcoom van corpus uteri (aandoening) | | rabdomyosarcoom van corpus uteri | | rabdomyosarcoom van baarmoederlichaam
| | Rhabdomyosarcoma of corpus uteri | | An extremely rare highly malignant soft tissue sarcoma located in the uterine body and arising from primitive mesenchymal cells displaying variable degrees of skeletal muscle differentiation. It most often presents with abnormal vaginal discharge or dysfunctional uterine bleeding, abdominal pain and lower abdominal mass. Association with DICER1 syndrome has been reported. |
| | DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | C54.2 | | Term | Maligne neoplasma van myometrium |
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| SNOMED CT to Orphanet simple map | 213615 |
| SNOMED CT to ICD-10 extended map | | Target | C54.2 | | Rule | TRUE | | Advice | ALWAYS C54.2 | MAPPED FOLLOWING WHO GUIDANCE | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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