238069004: Acyl-coenzyme A oxidase deficiency (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Inborn error of metabolism\...

\Disorder of peroxisomal function\Loss of single peroxisomal function\Acyl-CoA oxidase deficiency

\Inherited metabolic disorder of nervous system\Acyl-CoA oxidase deficiency

\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Acyl-CoA oxidase deficiency

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Acyl-CoA oxidase deficiency

\Degenerative disorder\Acyl-CoA oxidase deficiency

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Acyl-CoA oxidase deficiency
\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Acyl-CoA oxidase deficiency

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\...

\Disorder of peroxisomal function\Loss of single peroxisomal function\Acyl-CoA oxidase deficiency

\Inherited metabolic disorder of nervous system\Acyl-CoA oxidase deficiency

\Congenital disease\Inborn error of metabolism\...

\Disorder of peroxisomal function\Loss of single peroxisomal function\Acyl-CoA oxidase deficiency

\Inherited metabolic disorder of nervous system\Acyl-CoA oxidase deficiency

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

Descriptions:

Id Description Lang Type Status Case? Module

2971297015 Acyl-coenzyme A oxidase deficiency (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

2971496010 Acyl-coenzyme A oxidase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

3425921019 Peroxisomal acyl-CoA oxidase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

3425922014 Straight-chain acyl-CoA oxidase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

3521402019 Pseudoadrenoleukodystrophy en Synonym Active Case insensitive SNOMED CT core

356853013 Acyl-CoA oxidase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

356854019 Pseudo-neonatal adrenoleucodystrophy en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acyl-CoA oxidase deficiency	Is a	Loss of single peroxisomal function	true	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Is a	Degenerative disorder	true	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Occurrence	Congenital	true	Inferred relationship	Some	2
Acyl-CoA oxidase deficiency	Finding site	Structure of nervous system	true	Inferred relationship	Some	1
Acyl-CoA oxidase deficiency	Associated morphology	Degenerative abnormality	true	Inferred relationship	Some	1
Acyl-CoA oxidase deficiency	Is a	Inherited metabolic disorder of nervous system	true	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Occurrence	Congenital	false	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Finding site	Adrenal cortex structure	false	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Finding site	Entire endocrine gonad	false	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Is a	Adrenoleucodystrophy	false	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Occurrence	Congenital	false	Inferred relationship	Some	1
Acyl-CoA oxidase deficiency	Finding site	Adrenal cortex structure	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set