FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

124147007: Deficiency of xanthine oxidase (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
203590019 Deficiency of hypoxanthine oxidase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
203591015 Deficiency of xanthine oxidase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
473026015 Xanthine oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
727637011 Deficiency of xanthine oxidase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
862171000052113 xantinoxidasbrist sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


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

This concept is not in any reference sets

Back to Start