familial juvenile gout

Preferred Label : familial juvenile gout;

Origin ID

D6-40270;

UMLS CUI

C0268113;

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]
- familial juvenile hyperuricemic nephropathy [Disease (Nov.)]
- familial juvenile hyperuricemic nephropathy [DO Concept]
- juvenile gout [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Gout due to impairment of renal function [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- purine, nos [SNOMED Notion]
SNOMED CT concept
- Familial juvenile gout (disorder) [SNOMED CT 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]
- juvenile gout [MeSH concept]