Primary Hyperoxaluria Type III

Preferred Label : Primary Hyperoxaluria Type III;

Alternative definition : NICHD: Recessively inherited primary hyperoxaluria due to mitochondrial 4-hydroxy-2-oxoglutarate aldolase (HOGA1) gene mutations.;

Details

Origin ID

C123214;

UMLS CUI

C3150878;

Automatic exact mappings (from CISMeF team)
- primary hyperoxaluria type 3 [DO Concept]
Currated CISMeF NLP mapping
- Hyperoxaluria, primary, type III [OMIM Phenotype]
- Primary hyperoxaluria type 3 [ORDO Disease]
- Primary hyperoxaluria type III (disorder) [SNOMED CT concept]
- primary hyperoxaluria type III [Disease (Nov.)]
DO Cross reference
- primary hyperoxaluria type 3 [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperoxaluria, primary, type III [OMIM Phenotype]
- Primary hyperoxaluria type 3 [ORDO Disease]
- Primary hyperoxaluria type III (disorder) [SNOMED CT concept]
- primary hyperoxaluria type 3 [DO Concept]
- primary hyperoxaluria type III [Disease (Nov.)]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Nephrology Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients