230370006: Type V atypical Pelizaeus-Merzbacher disease (disorder)

SNOMED CT Concept\constatation clinique\...

\lésion neurologique\Leukodystrophy\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease

\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\...

\Leukodystrophy\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease

\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Genetic disease\maladie héréditaire\Sex-linked hereditary disorder\X-linked hereditary disease\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Leukodystrophy\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Neuropathy (disorder)\Leukodystrophy\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Leukodystrophy\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease
\Disease\trouble du développement\Developmental hereditary disorder\Pelizaeus-Merzbacher disease\Type V atypical Pelizaeus-Merzbacher disease

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

345208019 Type V atypical Pelizaeus-Merzbacher disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

618169015 Type V atypical Pelizaeus-Merzbacher disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Type V atypical Pelizaeus-Merzbacher disease	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
Type V atypical Pelizaeus-Merzbacher disease	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	morphologie associée (attribut)	Myelin sheath alteration	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	morphologie associée (attribut)	Myelin sheath alteration	true	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	localisation d'une constatation (attribut)	système nerveux	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	est un(e) (attribut)	Pelizaeus-Merzbacher disease	true	Inferred relationship	Some
Type V atypical Pelizaeus-Merzbacher disease	morphologie associée (attribut)	Sudanophilic stain reaction	false	Inferred relationship	Some	3
Type V atypical Pelizaeus-Merzbacher disease	survenue (attribut)	congénital	false	Inferred relationship	Some	4
Type V atypical Pelizaeus-Merzbacher disease	localisation d'une constatation (attribut)	système nerveux	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	true	Inferred relationship	Some	2
Type V atypical Pelizaeus-Merzbacher disease	localisation d'une constatation (attribut)	White matter structure of brain and spinal cord (body structure)	true	Inferred relationship	Some	2
Type V atypical Pelizaeus-Merzbacher disease	localisation d'une constatation (attribut)	Myelinated nerve fiber structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
345208019	Type V atypical Pelizaeus-Merzbacher disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
618169015	Type V atypical Pelizaeus-Merzbacher disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core