82319005: Acyl-coenzyme A dehydrogenase deficiency (disorder)

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

\Genetic disease\Hereditary disease\...

\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Acyl-CoA dehydrogenase deficiency

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatty acid oxidation defect (disorder)\Acyl-CoA dehydrogenase deficiency

\Metabolic disease\Disorder of organic acid metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Acyl-CoA dehydrogenase deficiency
\Metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Acyl-CoA dehydrogenase deficiency
\Metabolic disease\Enzymopathy\Acyl-CoA dehydrogenase deficiency
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Acyl-CoA dehydrogenase deficiency

\Congenital disease (disorder)\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Acyl-CoA dehydrogenase deficiency

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

136544017 Acyl-CoA dehydrogenase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2478870019 Deficiency of acyl-CoA dehydrogenase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2971050011 Acyl-coenzyme A dehydrogenase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2971966010 Acyl-coenzyme A dehydrogenase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

789851000052116 brist på acyl-CoA-dehydrogenas sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acyl-CoA dehydrogenase deficiency	Is a	Enzymopathy	true	Inferred relationship	Some
Acyl-CoA dehydrogenase deficiency	Is a	Disorder of fatty acid metabolism	false	Inferred relationship	Some
Acyl-CoA dehydrogenase deficiency	Occurrence	Congenital	true	Inferred relationship	Some	1
Acyl-CoA dehydrogenase deficiency	Finding site	Body system structure	false	Inferred relationship	Some
Acyl-CoA dehydrogenase deficiency	Is a	Fatty acid oxidation defect (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Long chain acyl-CoA dehydrogenase deficiency	Is a	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some
Very long chain acyl-CoA dehydrogenase deficiency	Is a	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency	Is a	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some
Medium-chain acyl-coenzyme A dehydrogenase deficiency	Is a	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some
Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9 (disorder)	Due to	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some	2
Short chain acyl-coenzyme A dehydrogenase deficiency (disorder)	Is a	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some
Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)	Is a	True	Acyl-CoA dehydrogenase deficiency	Inferred relationship	Some

This concept is not in any reference sets