238059005: Disorder 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

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function

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

356841014 Disorder of peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626890017 Disorder of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

356841014 Disorder of peroxisomal function en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356841014 Disorder of peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626890017 Disorder of peroxisomal function (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626890017 Disorder of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3452211001000112 Peroxisomale Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6072061000241110 trouble de la fonction peroxysomale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6072071000241119 trouble de la fonction des peroxysomes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6072061000241110 trouble de la fonction peroxysomale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6072071000241119 trouble de la fonction des peroxysomes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3452211001000112 Peroxisomale Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Disorder of peroxisomal function	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Disorder of peroxisomal function	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Disorder of peroxisomal function	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
General loss of peroxisomal function (disorder)	Is a	True	Disorder of peroxisomal function	Inferred relationship	Existential restriction modifier (core metadata concept)
Loss of multiple peroxisomal functions (disorder)	Is a	True	Disorder of peroxisomal function	Inferred relationship	Existential restriction modifier (core metadata concept)
Loss of single peroxisomal function (disorder)	Is a	True	Disorder of peroxisomal function	Inferred relationship	Existential restriction modifier (core metadata concept)
Peroxisome biogenesis disorder (disorder)	Is a	True	Disorder of peroxisomal function	Inferred relationship	Existential restriction modifier (core metadata concept)
Liver disease due to peroxisomal disease	Due to	True	Disorder of peroxisomal function	Inferred relationship	Existential restriction modifier (core metadata concept)	2

This concept is not in any reference sets