238003000: Carnitine acylcarnitine translocase deficiency (disorder)

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\...

\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Carnitine acylcarnitine translocase deficiency

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatty acid oxidation defect (disorder)\Carnitine acylcarnitine translocase deficiency

\trouble métabolique\Disorder of organic acid metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Carnitine acylcarnitine translocase deficiency
\trouble métabolique\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Carnitine acylcarnitine translocase deficiency
\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Carnitine acylcarnitine translocase deficiency

\Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect (disorder)\Carnitine acylcarnitine translocase 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

356730018 Carnitine acylcarnitine translocase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

549561000241112 déficit en carnitine-acylcarnitine translocase (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

626819017 Carnitine acylcarnitine translocase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

960681000172117 déficit en carnitine-acylcarnitine translocase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

990731000172110 déficit en CACT (carnitine-acylcarnitine translocase) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Carnitine acylcarnitine translocase deficiency	est un(e) (attribut)	Fatty acid oxidation defect (disorder)	true	Inferred relationship	Some
Carnitine acylcarnitine translocase deficiency	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Carnitine acylcarnitine translocase deficiency	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Carnitine acylcarnitine translocase deficiency	est un(e) (attribut)	Disorder of fatty acid metabolism	false	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets