| Potter-syndroom (aandoening) | | Potter-syndroom | | syndroom van Potter
renofaciale dysplasie
| | syndroom van Potter | | Zeldzame aangeboren aandoening met als voornaamste kenmerken afwezigheid van nierweefsel en ernstige misvorming van de nieren, karakteristieke gelaatskenmerken en niet goed ontwikkelde longen. | | Oligohydramnios sequence | | BRA - Bilateral renal agenesis
Potter's anomaly of the kidney
Bilateral congenital absence of kidneys
Potter syndrome
Renofacial syndrome
Renal agenesis syndrome
Congenital absence of kidneys syndrome
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| | Id | 41962002 | | Status | Primitive |
| PALGA thesaurus simple reference set for pathology |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q60.6 | | Term | Syndroom van Potter |
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| SNOMED CT to ICD-10 extended map | | Target | Q60.6 | | Rule | TRUE | | Advice | ALWAYS Q60.6 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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