238060000: General loss of peroxisomal function (disorder)

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

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\General loss of peroxisomal function (disorder)

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\General loss of peroxisomal function (disorder)

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\General loss of peroxisomal function (disorder)

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

356842019 General loss of peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626891018 General loss of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

356842019 General loss of peroxisomal function en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356842019 General loss of peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626891018 General loss of peroxisomal function (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626891018 General loss of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6302111000241115 perte générale de la fonction peroxysomale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6302121000241110 perte générale de la fonction des peroxysomes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6302111000241115 perte générale de la fonction peroxysomale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6302121000241110 perte générale de la fonction des peroxysomes 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
General loss of peroxisomal function (disorder)	Is a	Disorder of peroxisomal function	true	Inferred relationship	Existential restriction modifier (core metadata concept)
General loss of peroxisomal function (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
General loss of peroxisomal function (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Neonatal adrenoleucodystrophy	Is a	False	General loss of peroxisomal function (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Infantile Refsum's disease	Is a	False	General loss of peroxisomal function (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-methylacyl-CoA racemase deficiency disorder	Is a	True	General loss of peroxisomal function (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets