bartter syndrome, type 3, with hypocalciuria

Preferred Label : bartter syndrome, type 3, with hypocalciuria;

MeSH note : mutation in CLCNKB;

Origin ID

C564578;

UMLS CUI

C1846344;

Automatic exact mappings (from CISMeF team)
- Bartter syndrome, type 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- bartter syndrome [MeSH Descriptor]
Record concept(s)
- bartter syndrome, type 3, with hypocalciuria [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]