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238006008: Disorder of purine and pyrimidine metabolism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3036760010 Purine and pyrimidine metabolism disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356736012 Disorder of purine and pyrimidine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626823013 Disorder of purine and pyrimidine metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


186 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of purine and pyrimidine metabolism est un(e) (attribut) trouble métabolique true Inferred relationship Some
Disorder of purine and pyrimidine metabolism localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Disorder of purine and pyrimidine metabolism survenue (attribut) congénital false Inferred relationship Some
Disorder of purine and pyrimidine metabolism est un(e) (attribut) Inborn error of metabolism false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Deficiency of xanthine oxidase est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
troubles du métabolisme des purines est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
Hereditary orotic aciduria, type 1 est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
Congenital hypoplastic anemia est un(e) (attribut) False Disorder of purine and pyrimidine metabolism Inferred relationship Some
Hereditary orotic aciduria, type 2 est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
Xanthinuria est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
Other disorders of purine and pyrimidine metabolism est un(e) (attribut) False Disorder of purine and pyrimidine metabolism Inferred relationship Some
Uridine monophosphate hydrolase deficiency est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
Cytosine diphosphate choline phosphotransferase deficiency est un(e) (attribut) True Disorder of purine and pyrimidine metabolism Inferred relationship Some
Dihydropyrimidinase deficiency est un(e) (attribut) False Disorder of purine and pyrimidine metabolism Inferred relationship Some
Dihydropyrimidine dehydrogenase deficiency est un(e) (attribut) False Disorder of purine and pyrimidine metabolism Inferred relationship Some
X-linked hyperuricemia est un(e) (attribut) False Disorder of purine and pyrimidine metabolism Inferred relationship Some

This concept is not in any reference sets

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