5-oxoprolinase deficiency

Preferred Label : 5-oxoprolinase deficiency;

Origin ID

D6-A3570;

UMLS CUI

C0268525;

Currated CISMeF NLP mapping
- 5-Oxoprolinase deficiency (disorder) [SNOMED CT concept]
- 5-oxoprolinase deficiency [MeSH Supplementary Concept]
- 5-oxoprolinase deficiency [MeSH concept]
- 5-oxoprolinase deficiency [OMIM Phenotype]
- 5-oxoprolinase deficiency [ORDO Disease]
- Oxoprolinuria [ICD-11 More detail]
- Reduced 5-oxoprolinase level [HPO term]
ICD-10 exact mapping(s)
- Other specified disorders of amino-acid metabolism [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- 5-Oxoprolinase deficiency (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 5-Oxoprolinase deficiency (disorder) [SNOMED CT concept]
- 5-oxoprolinase deficiency [MeSH Supplementary Concept]
- 5-oxoprolinase deficiency [ORDO Disease]
- 5-oxoprolinase deficiency [OMIM Phenotype]
- 5-oxoprolinase deficiency [MeSH concept]
- Oxoprolinuria [ICD-11 More detail]
- Reduced 5-oxoprolinase level [HPO term]