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-coenzyme A oxidase deficiency

\Inherited metabolic disorder of nervous system\Acyl-coenzyme A oxidase deficiency

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

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Acyl-coenzyme A oxidase deficiency

\Degenerative disorder\Acyl-coenzyme A oxidase deficiency

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Acyl-coenzyme A oxidase deficiency
\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Acyl-coenzyme A oxidase deficiency

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

\Disorder of peroxisomal function\Loss of single peroxisomal function\Acyl-coenzyme A oxidase deficiency

\Inherited metabolic disorder of nervous system\Acyl-coenzyme A oxidase deficiency

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

\Disorder of peroxisomal function\Loss of single peroxisomal function\Acyl-coenzyme A oxidase deficiency

\Inherited metabolic disorder of nervous system\Acyl-coenzyme A oxidase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

356853013 Acyl-CoA oxidase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

356854019 Pseudo-neonatal adrenoleucodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

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

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

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

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

3521402019 Pseudoadrenoleukodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

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Characteristic

Refinability

Group

This concept is not in any reference sets