hypocalcemia, autosomal dominant, with bartter syndrome - CISMeF

" /> hypocalcemia, autosomal dominant, with bartter syndrome - CISMeF

CISMeF

chu

Hypocalcemia, autosomal dominant, with bartter syndromeMeSH Supplementary Concept

Preferred Label : hypocalcemia, autosomal dominant, with bartter syndrome;

Details

Origin ID

C563374;

UMLS CUI

C1832612;

MeSH term(s) associated for indexing
- bartter syndrome [MeSH Descriptor]
- hypocalcemia [MeSH Descriptor]
Record concept(s)
- hypocalcemia, autosomal dominant, with bartter syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
03/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.