low molecular weight proteinuria with hypercalciuria and nephrocalcinosis

Preferred Label : low molecular weight proteinuria with hypercalciuria and nephrocalcinosis;

MeSH synonym : proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis;

Détails

Origin ID

C545036;

UMLS CUI

C1839874;

Automatic exact mappings (from CISMeF team)
- Dent disease [ORDO Disease]
- Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [OMIM Phenotype]
Has phenotype(s) (HPO)
- focal glomerulosclerosis [HPO term]
MeSH term(s) associated for indexing
- dent disease [MeSH Descriptor]
ORDO relation(s)
- Dent disease [ORDO Disease]
Record concept(s)
- Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [OMIM Phenotype]

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

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