juvenile gout - CISMeF

Preferred Label : juvenile gout;

CISMeF synonym : familial juvenile hyperuricaemic nephropathy;

MeSH synonym : gouty nephropathy, familial juvenile; nephropathy, familial, with gout; hyperuricemic nephropathy, familial juvenile; hyperuricemic nephropathy, familial juvenile 1; familial juvenile hyperuricemic nephropathy; Umod-Related kidney disease; Uromodulin-Associated kidney disease; familial Gout-Kidney disease; familial gouty nephropathy; Mckd2; medullary cystic kidney disease type 2; uromodulin storage disease; HNFJ1; HNFJ;

Details

Origin ID

C537696;

UMLS CUI

C4551496;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant tubulointerstitial disease Type 2 [ICD-11 More detail]
- Autosomal dominant tubulointerstitial kidney disease [ORDO Disease]
- Tubulointerstitial kidney disease [OMIM phenotypic series]
- 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]
- familial juvenile gout [SNOMED Notion]
- familial juvenile hyperuricemic nephropathy [DO Concept]
- familial juvenile hyperuricemic nephropathy [Disease (Nov.)]
MeSH term(s) associated for indexing
- gout [MeSH Descriptor]
- hyperuricemia [MeSH Descriptor]
- kidney diseases [MeSH Descriptor]
Record concept(s)
- juvenile gout [MeSH concept]
See also inter- (CISMeF)
- Medullary Cystic Kidney Disease Type II [NCIt concept]
- Medullary cystic kidney disease 2 [OMIM Phenotype]
- Medullary cystic kidney disease type 2 (disorder) [Inactive SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Tubulointerstitial kidney disease, autosomal dominant, 1 [OMIM Phenotype]

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