Primary Hyperoxaluria

Preferred Label : Primary Hyperoxaluria;

Alternative definition : NICHD: A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.;

Details

Origin ID

C123158;

UMLS CUI

C0020501;

Automatic exact mappings (from CISMeF team)
- Hyperoxaluria, primary [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Primary hyperoxaluria [ORDO Disease]
- Primary hyperoxaluria [MedDRA Preferred Term]
- Primary hyperoxaluria (disorder) [SNOMED CT concept]
- hyperoxaluria, primary [MeSH Descriptor]
- hyperoxaluria, primary [MeSH concept]
- primary hyperoxaluria [DO Concept]
- primary hyperoxaluria [Disease (Nov.)]
- primary hyperoxaluria, nos [SNOMED Notion]
DO Cross reference
- primary hyperoxaluria [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Primary hyperoxaluria [ORDO Disease]
- Primary hyperoxaluria [MedDRA Preferred Term]
- Primary hyperoxaluria (disorder) [SNOMED CT concept]
- hyperoxaluria, primary [MeSH Descriptor]
- hyperoxaluria, primary [MeSH concept]
- primary hyperoxaluria [DO Concept]
- primary hyperoxaluria [Disease (Nov.)]
- primary hyperoxaluria, nos [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Nephrology Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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