FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

238069004: Acyl-coenzyme A oxidase deficiency (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
356853013 Acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356854019 Pseudo-neonatal adrenoleucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2971297015 Acyl-coenzyme A oxidase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2971496010 Acyl-coenzyme A oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3425921019 Peroxisomal acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3425922014 Straight-chain acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3521402019 Pseudoadrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356853013 Acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356854019 Pseudo-neonatal adrenoleucodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356854019 Pseudo-neonatal adrenoleucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626901013 Acyl-CoA oxidase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2971297015 Acyl-coenzyme A oxidase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2971496010 Acyl-coenzyme A oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3425921019 Peroxisomal acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3425921019 Peroxisomal acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3425922014 Straight-chain acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3425922014 Straight-chain acyl-CoA oxidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3521402019 Pseudoadrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3386611001000113 Acyl-CoA-Oxidase-Mangel, peroxisomaler de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5021761000241116 déficit en acyl-CoA oxidase fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5021761000241116 déficit en acyl-CoA oxidase fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386611001000113 Acyl-CoA-Oxidase-Mangel, peroxisomaler de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acyl-coenzyme A oxidase deficiency (disorder) Is a Adrenoleukodystrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acyl-coenzyme A oxidase deficiency (disorder) Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acyl-coenzyme A oxidase deficiency (disorder) Is a Loss of single peroxisomal function (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Is a Degenerative disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Acyl-coenzyme A oxidase deficiency (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Acyl-coenzyme A oxidase deficiency (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acyl-coenzyme A oxidase deficiency (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acyl-coenzyme A oxidase deficiency (disorder) Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start