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85444005: Disorder of 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
141631019 Disorder of pyrimidine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
476241000241113 trouble du métabolisme de la pyrimidine (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
827499018 Disorder of pyrimidine metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
890761000172113 trouble du métabolisme de la pyrimidine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


12 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder) est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some
Beta-aminoisobutyric aciduria (disorder) est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some
Orotic aciduria (disorder) est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some
Dihydropyrimidine dehydrogenase deficiency est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some
Cytosine diphosphate choline phosphotransferase deficiency est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some
Dihydropyrimidinase deficiency est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some
Solute carrier family 35 member A1 congenital disorder of glycosylation (disorder) est un(e) (attribut) True Disorder of pyrimidine metabolism Inferred relationship Some

This concept is not in any reference sets

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