238063003: Loss of multiple peroxisomal functions (disorder)

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

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of multiple peroxisomal functions (disorder)

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of multiple peroxisomal functions (disorder)

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of multiple peroxisomal functions (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

356845017 Loss of multiple peroxisomal functions en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626894014 Loss of multiple peroxisomal functions (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

356845017 Loss of multiple peroxisomal functions en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356845017 Loss of multiple peroxisomal functions en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626894014 Loss of multiple peroxisomal functions (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626894014 Loss of multiple peroxisomal functions (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6392081000241110 perte de plusieurs fonctions peroxysomales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6392091000241112 perte de multiples fonctions peroxysomales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6392081000241110 perte de plusieurs fonctions peroxysomales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6392091000241112 perte de multiples fonctions peroxysomales 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
Loss of multiple peroxisomal functions (disorder)	Is a	Disorder of peroxisomal function	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Loss of multiple peroxisomal functions (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Loss of multiple peroxisomal functions (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Zellweger's-like syndrome (disorder)	Is a	True	Loss of multiple peroxisomal functions (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudoinfantile Refsum's disease	Is a	True	Loss of multiple peroxisomal functions (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Rhizomelic chondrodysplasia punctata syndrome	Is a	True	Loss of multiple peroxisomal functions (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets