| syndroom van hyperurikemie, anemie en nierfalen (aandoening) | | syndroom van hyperurikemie, anemie en nierfalen | | syndroom van hyperurikemie, bloedarmoede en nierinsufficiëntie
| | Hyperuricemia, anemia, renal failure syndrome | | Familial juvenile hyperuricemic nephropathy type 2
Renin associated familial juvenile hyperuricemic nephropathy
| | A rare autosomal dominant tubulointerstitial kidney disease (ADTKD) of childhood due to REN mutations and characterized by early onset hypoproliferative anemia, hyperuricemia, gout, and slowly progressive tubulointerstitial kidney disease. |
| | Id | 721840000 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 217330 |
| 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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