1187550009: Peroxisome biogenesis disorder due to PEX6 mutation (disorder)

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

\Genetic disease\maladie héréditaire\...

\Inborn error of metabolism\Disorder of peroxisomal function\Peroxisome biogenesis disorder\PEX6 deficiency

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Peroxisome biogenesis disorder\PEX6 deficiency

\trouble métabolique\Inborn error of metabolism\Disorder of peroxisomal function\Peroxisome biogenesis disorder\PEX6 deficiency

\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Peroxisome biogenesis disorder\PEX6 deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4674131017 PEX6 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4674520018 Peroxisome biogenesis disorder due to PEX6 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4674521019 Peroxisome biogenesis disorder due to PEX6 mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
PEX6 deficiency	survenue (attribut)	congénital	true	Inferred relationship	Some	1
PEX6 deficiency	est un(e) (attribut)	Peroxisome biogenesis disorder	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set