230371005: Type VI Cockayne Pelizaeus-Merzbacher disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Neurological lesion\Leukodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease

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

\Leukodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease

\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type VI Cockayne 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\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Leukodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type VI Cockayne 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\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system\Neuropathy\Leukodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Leukodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
\Disease\Developmental disorder\Developmental hereditary disorder\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

345209010 Type VI Cockayne Pelizaeus-Merzbacher disease en Synonym Active Entire term case sensitive SNOMED CT core module

618170019 Type VI Cockayne Pelizaeus-Merzbacher disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Type VI Cockayne Pelizaeus-Merzbacher disease	Is a	Pelizaeus-Merzbacher disease	true	Inferred relationship	Existential restriction modifier
Type VI Cockayne Pelizaeus-Merzbacher disease	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	4
Type VI Cockayne Pelizaeus-Merzbacher disease	Associated morphology	Sudanophilic stain reaction	false	Inferred relationship	Existential restriction modifier	3
Type VI Cockayne Pelizaeus-Merzbacher disease	Associated morphology	Myelin sheath alteration	false	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Associated morphology	Myelin sheath alteration	true	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier	2
Type VI Cockayne Pelizaeus-Merzbacher disease	Finding site	Myelinated nerve fiber structure	true	Inferred relationship	Existential restriction modifier	1
Type VI Cockayne Pelizaeus-Merzbacher disease	Finding site	White matter structure of brain and spinal cord	true	Inferred relationship	Existential restriction modifier	2
Type VI Cockayne Pelizaeus-Merzbacher disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Type VI Cockayne Pelizaeus-Merzbacher disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	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
345209010	Type VI Cockayne Pelizaeus-Merzbacher disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
618170019	Type VI Cockayne Pelizaeus-Merzbacher disease (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module