Hypouricemia, familial renal, due to tubular hypersecretion

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

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked;

Prefixed ID : 307830;

Details

Origin ID

307830;

UMLS CUI

C1843972;

Currated CISMeF NLP mapping
- Hereditary renal hypouricemia [ORDO Disease]
- hypouricemia, familial renal, due to tubular hypersecretion [MeSH concept]
- hypouricemia, familial renal, due to tubular hypersecretion [MeSH Supplementary Concept]
HPO term(s)
- Chronic hereditary nephritis [HPO term]
- Hypouricemia [HPO term]
- X-linked recessive inheritance [HPO term]
ORDO concept(s)
- Hereditary renal hypouricemia [ORDO Disease]
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 [MeSH Supplementary Concept]
- hypouricemia, familial renal, due to tubular hypersecretion [MeSH concept]

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