| autosomaal dominante tubulo-interstitiële nierziekte (aandoening) | | autosomaal dominante tubulo-interstitiële nierziekte | | MCKD
ADTKD
autosomaal dominante medullaire cystische nierziekte
medullary cystic kidney disease
medullaire cystenieren
| | Autosomal dominant tubulointerstitial kidney disease | | Autosomal dominant medullary cystic kidney disease
| | A rare, genetic renal tubular disease characterized by tubular damage and interstitial fibrosis in absence of glomerular lesions and clinically manifesting with chronic kidney disease (CKD) and slow progression to end-stage kidney disease (ESKD). |
| | Id | 726018006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to ICD-10 extended map | | Target | Q61.5 | | Rule | TRUE | | Advice | ALWAYS Q61.5 | 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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| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q61.5 | | Term | Medullair-cystische nier |
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