Disorder of purine and pyrimidine metabolism, unspecified

Preferred Label : Disorder of purine and pyrimidine metabolism, unspecified;

Imprécision du diag : 1;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E799;

UMLS CUI

C0034139;

CISMeF manual mappings
- Disorder of purine and pyrimidine metabolism (disorder) [SNOMED CT concept]
Manual NTBT mappings (CISMeF)
- Disorder of purine metabolism [ORDO Disease]
- Disorder of pyrimidine metabolism [ORDO Disease]
Orphanet concepts
- Disorder of purine or pyrimidine metabolism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder of purine and pyrimidine metabolism (disorder) [SNOMED CT concept]
- Disorder of purine or pyrimidine metabolism [ORDO Disease]
- Inborn errors of purine, pyrimidine or nucleotide metabolism [ICD-11 Category]
- Purine and pyrimidine metabolism disorders [MedDRA High Level Group Term]
- Purine-Pyrimidine metabolism, inborn errors [MeSH concept]
- disorders of purine and pyrimidine metabolism [Disease (Nov.)]
- purine-pyrimidine metabolism, inborn errors [MeSH Descriptor]
Validated automatic mappings to NTBT
- disorders of purine and pyrimidine metabolism [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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