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

• SNOMED CT Concept\Clinical finding (finding)\...
• \Neurological lesion\Leucodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne 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\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 (disorder)\Hereditary disorder of nervous system (disorder)\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 (disorder)\X-linked hereditary disease\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
• \Disease\Degenerative disorder\Degenerative disease of the central nervous system\Leucodystrophy\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 (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Leucodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Leucodystrophy\Pelizaeus-Merzbacher disease\Type VI Cockayne Pelizaeus-Merzbacher disease
• \Disease\Disorder of body system\Disease 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\Type VI Cockayne Pelizaeus-Merzbacher disease
• \Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Pelizaeus-Merzbacher disease\Type VI Cockayne 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
345209010	Type VI Cockayne Pelizaeus-Merzbacher disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
618170019	Type VI Cockayne Pelizaeus-Merzbacher disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
345209010	Type VI Cockayne Pelizaeus-Merzbacher disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
618170019	Type VI Cockayne Pelizaeus-Merzbacher disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
618170019	Type VI Cockayne Pelizaeus-Merzbacher disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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