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85444005: Disorder of pyrimidine metabolism (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
141631019 Disorder of pyrimidine metabolism en Synonym Active Case insensitive SNOMED CT core
827499018 Disorder of pyrimidine metabolism (disorder) en Fully specified name Active Case insensitive SNOMED CT core

12 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of pyrimidine metabolism Is a Inborn error of metabolism false Inferred relationship Some
Disorder of pyrimidine metabolism Is a Metabolic disease true Inferred relationship Some
Disorder of pyrimidine metabolism Finding site Body system structure false Inferred relationship Some
Disorder of pyrimidine metabolism Occurrence Congenital false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form Is a True Disorder of pyrimidine metabolism Inferred relationship Some
Beta-aminoisobutyric aciduria Is a True Disorder of pyrimidine metabolism Inferred relationship Some
Orotic aciduria Is a True Disorder of pyrimidine metabolism Inferred relationship Some
Dihydrouracil dehydrogenase (NADP^+^) deficiency Is a True Disorder of pyrimidine metabolism Inferred relationship Some
Cytosine diphosphate choline phosphotransferase deficiency Is a True Disorder of pyrimidine metabolism Inferred relationship Some
Dihydropyrimidinase deficiency Is a True Disorder of pyrimidine metabolism Inferred relationship Some
SLC35A1 congenital disorder of glycosylation Is a True Disorder of pyrimidine metabolism Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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