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124147007: Deficiency of xanthine oxidase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
203590019 Deficiency of hypoxanthine oxidase en Synonym Active Case insensitive SNOMED CT core
203591015 Deficiency of xanthine oxidase en Synonym Active Case insensitive SNOMED CT core
473026015 Xanthine oxidase deficiency en Synonym Active Case insensitive SNOMED CT core
727637011 Deficiency of xanthine oxidase (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of xanthine oxidase Is a Specific enzyme deficiency true Inferred relationship Some
Deficiency of xanthine oxidase Is a Metabolic renal disease true Inferred relationship Some
Deficiency of xanthine oxidase Is a Hereditary disorder of the urinary system false Inferred relationship Some
Deficiency of xanthine oxidase Is a Purine and pyrimidine metabolism disorder true Inferred relationship Some
Deficiency of xanthine oxidase Is a Congenital anomaly of trunk false Inferred relationship Some
Deficiency of xanthine oxidase Occurrence Congenital false Inferred relationship Some
Deficiency of xanthine oxidase Finding site Kidney structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary xanthinuria type 1 Due to True Deficiency of xanthine oxidase Inferred relationship Some 1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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