azotemia, familial

Preferred Label : azotemia, familial;

Origin ID

C566233;

UMLS CUI

C1862358;

Currated CISMeF NLP mapping
- Azotemia, familial [OMIM Phenotype]
MeSH term(s) associated for indexing
- renal tubular transport, inborn errors [MeSH Descriptor]
Record concept(s)
- azotemia, familial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Azotemia, familial [OMIM Phenotype]