| X-gebonden mentale retardatie door PQBP1-mutatie (aandoening) | | X-gebonden mentale retardatie door PQBP1-mutatie | | X-gebonden mentale retardatie Renpenning-type
syndroom van Renpenning
| | Renpenning syndrome | | Porteous syndrome
Sutherland-Haan syndrome
Golabi-Ito-Hall syndrome
X-linked intellectual deficit due to PQBP1 mutation
Hamel cerebropalatocardiac syndrome
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| | Id | 699669001 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.5 | | Term | Overige congenitale gestoorde-ontwikkelingssyndromen met overige skeletveranderingen |
|
| SNOMED CT to Orphanet simple map | 3242 |
| SNOMED CT to ICD-10 extended map | | Target | Q87.5 | | Rule | TRUE | | Advice | ALWAYS Q87.5 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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