hypouricemia, familial renal, due to tubular hypersecretion

Preferred Label : hypouricemia, familial renal, due to tubular hypersecretion;

Origin ID

C564405;

UMLS CUI

C1843972;

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