| Mowat-Wilson-syndroom (aandoening) | | Mowat-Wilson-syndroom | | syndroom van Mowat-Wilson
syndroom van ziekte van Hirschsprung en mentale retardatie
syndroom van ziekte van Hirschsprung en verstandelijke handicap
syndroom van ziekte van Hirschsprung en verstandelijke beperking
| | Mowat-Wilson syndrome | | Hirschsprung disease-mental retardation syndrome
Hirschsprung disease-intellectual disability syndrome
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| | Id | 703535000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.8 | | Term | Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd |
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| SNOMED CT to Orphanet simple map | 2152 |
| SNOMED CT to ICD-10 extended map | | Target | Q43.1 | | Rule | TRUE | | Advice | ALWAYS Q43.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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