230370006: ziekte van Pelizaeus-Merzbacher type 5 (aandoening)

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

\Neurological lesion\Leucodystrophy\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease

\Central nervous system finding\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\...

\Leucodystrophy\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Leucodystrophy\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neuropathy (disorder)\Leucodystrophy\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Leucodystrophy\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease (disorder)\Type V atypical Pelizaeus-Merzbacher disease
\Disease\Developmental disorder\Developmental hereditary disorder\Pelizaeus-Merzbacher disease (disorder)\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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Type V atypical Pelizaeus-Merzbacher disease	Is a	Pelizaeus-Merzbacher disease (disorder)	true	Inferred relationship	Some
Type V atypical Pelizaeus-Merzbacher disease	Associated morphology	Sudanophilic stain reaction	false	Inferred relationship	Some	3
Type V atypical Pelizaeus-Merzbacher disease	Occurrence	Congenital	false	Inferred relationship	Some	4
Type V atypical Pelizaeus-Merzbacher disease	Finding site	Structure of nervous system (body structure)	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Associated morphology	Myelin sheath alteration	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Associated morphology	Myelin sheath alteration	true	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Finding site	Structure of nervous system (body structure)	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
Type V atypical Pelizaeus-Merzbacher disease	Associated morphology	Dystrophy	true	Inferred relationship	Some	2
Type V atypical Pelizaeus-Merzbacher disease	Finding site	White matter structure of brain and spinal cord (body structure)	true	Inferred relationship	Some	2
Type V atypical Pelizaeus-Merzbacher disease	Finding site	Myelinated nerve fiber structure	true	Inferred relationship	Some	1
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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
6989811000146114	ziekte van Pelizaeus-Merzbacher type 5	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
11327061000146111	ziekte van Pelizaeus-Merzbacher type 5 (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
11327071000146117	PMD type 5	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
11327081000146115	atypische vorm van Pelizaeus-Merzbacher-syndroom	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)