90500005: Carnitine palmitoyltransferase deficiency (disorder)

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

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism (disorder)\Carnitine palmitoyltransferase deficiency

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism (disorder)\Carnitine palmitoyltransferase deficiency

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism (disorder)\Carnitine palmitoyltransferase deficiency
\Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of fatty acid metabolism (disorder)\Carnitine palmitoyltransferase deficiency
\Metabolic disease\Enzymopathy\Carnitine palmitoyltransferase deficiency
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism (disorder)\Carnitine palmitoyltransferase 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

149995013 Carnitine palmitoyltransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

833617017 Carnitine palmitoyltransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

149995013 Carnitine palmitoyltransferase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

149995013 Carnitine palmitoyltransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

833617017 Carnitine palmitoyltransferase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

833617017 Carnitine palmitoyltransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4686551000241113 déficit en carnitine palmitoyltransférase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4686551000241113 déficit en carnitine palmitoyltransférase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Carnitine palmitoyltransferase deficiency	Is a	Enzymopathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Carnitine palmitoyltransferase deficiency	Is a	Disorder of fatty acid metabolism (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Carnitine palmitoyltransferase deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Carnitine palmitoyltransferase deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Carnitine palmitoyltransferase I deficiency	Is a	True	Carnitine palmitoyltransferase deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Carnitine palmitoyltransferase II deficiency (disorder)	Is a	True	Carnitine palmitoyltransferase deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets