juvenile gout - CISMeF

Preferred Label : juvenile gout;

CISMeF synonym : Familial juvenile hyperuricaemic nephropathy;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0532157;

UMLS CUI

C0268113;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant tubulointerstitial kidney disease [ORDO Disease]
- UMOD-related autosomal dominant tubulointerstitial kidney disease [ORDO Disease]
Currated CISMeF NLP mapping
- Familial juvenile gout (disorder) [SNOMED CT concept]
- Familial juvenile hyperuricaemic nephropathy [ICD-11 More detail]
- Familial juvenile hyperuricemic nephropathy type 1 [ORDO Disease]
- Tubulointerstitial kidney disease, autosomal dominant, 1 [OMIM Phenotype]
Related record
- juvenile gout [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial juvenile gout (disorder) [SNOMED CT concept]
- Familial juvenile hyperuricemic nephropathy type 1 [ORDO Disease]
- Tubulointerstitial kidney disease, autosomal dominant, 1 [OMIM Phenotype]
- familial juvenile gout [SNOMED Notion]
Validated automatic mappings to BTNT
- familial juvenile hyperuricemic nephropathy [Disease (Nov.)]

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