106018006: Hereditary degenerative disease of central nervous system (disorder)

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

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system
\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

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

170437013 Hereditary degenerative disease of central nervous system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

577254011 Hereditary degenerative disease of central nervous system (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2662611000052118 ärftlig degenerativ sjukdom i centrala nervsystemet sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary degenerative disease of central nervous system	Is a	Degenerative disease of the central nervous system	true	Inferred relationship	Some
Hereditary degenerative disease of central nervous system	Associated morphology	degeneration	false	Inferred relationship	Some	1
Hereditary degenerative disease of central nervous system	Finding site	Structure of central nervous system (body structure)	false	Inferred relationship	Some	1
Hereditary degenerative disease of central nervous system	Associated morphology	degeneration	false	Inferred relationship	Some	1
Hereditary degenerative disease of central nervous system	Finding site	Structure of central nervous system (body structure)	true	Inferred relationship	Some	1
Hereditary degenerative disease of central nervous system	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Some	1
Hereditary degenerative disease of central nervous system	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder)	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
Aicardi Goutieres syndrome type 2	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
Aicardi Goutieres syndrome type 3	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
Aicardi Goutieres syndrome type 4 (disorder)	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
Aicardi Goutieres syndrome type 5 (disorder)	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
Aicardi Goutieres syndrome type 1	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
Integral membrane protein 2B related amyloidosis (disorder)	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some
VPS11-related autosomal recessive hypomyelinating leukodystrophy	Is a	True	Hereditary degenerative disease of central nervous system	Inferred relationship	Some

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This concept is not in any reference sets