| progeria met kort gestalte en gepigmenteerde naevi (aandoening) | | progeria met kort gestalte en gepigmenteerde naevi | | Mulvihill-Smith-syndroom
| | Progeroid short stature with pigmented nevi | | Mulvihill-Smith syndrome
Baraitser syndrome
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| | Id | 399947002 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.1 | | Term | Congenitale gestoorde-ontwikkelingssyndromen voornamelijk gepaard gaande met kleine gestalte |
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| SNOMED CT to ICD-10 extended map | | Target | Q87.1 | | Rule | TRUE | | Advice | ALWAYS Q87.1 | 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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