hyperuricemic nephropathy, familial juvenile 2

Preferred Label : hyperuricemic nephropathy, familial juvenile 2;

MeSH synonym : Hnfj2; Early-Onset hyperuricemia, anemia, and progressive kidney failure; Familial Juvenile Hyperuricemic Nephropathy 2; Ren-Related Kidney Disease;

Détails

Origin ID

C567760;

UMLS CUI

C2751310;

Currated CISMeF NLP mapping
- Hyperuricemia, anemia, renal failure syndrome (disorder) [SNOMED CT concept]
- REN-related autosomal dominant tubulointerstitial kidney disease [ORDO Disease]
- Tubulointerstitial kidney disease, autosomal dominant, 4 [OMIM Phenotype]
MeSH term(s) associated for indexing
- anemia [MeSH Descriptor]
- hyperuricemia [MeSH Descriptor]
- renal insufficiency [MeSH Descriptor]
- renin [MeSH Descriptor]
Record concept(s)
- hyperuricemic nephropathy, familial juvenile 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- REN-related autosomal dominant tubulointerstitial kidney disease [ORDO Disease]
- Tubulointerstitial kidney disease, autosomal dominant, 4 [OMIM Phenotype]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients