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91502009: Spinocerebellar disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
151586018 Spinocerebellar disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
834831014 Spinocerebellar disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
151586018 Spinocerebellar disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
151586018 Spinocerebellar disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
834831014 Spinocerebellar disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
834831014 Spinocerebellar disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
196801000077117 maladie spinocérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
196801000077117 maladie spinocérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

82 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spinocerebellar disease Is a Disorder of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar disease Is a System disorders of the nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar disease Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar disease Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spinocerebellar disease Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spinocerebellar disease Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spinocerebellar disease Is a Cerebellar disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar disease Is a Encephalomyelopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar disease Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Friedreich ataxia (disorder) Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar disorder Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar deficiency syndrome (disorder) Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic cerebellar degeneration Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary amblyopia with quadriplegia in the Irish Setter Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spastic paraplegia Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Corticostriatal-spinal degeneration Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Roussy-Lévy syndrome Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Jervis' syndrome (disorder) Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Athetosis with spastic paraplegia Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Bailey-Cushing syndrome Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Paramyoclonus multiplex Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Ataxia-telangiectasia syndrome Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Primary progressive cerebellar degeneration (disorder) Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Posthemiplegic ataxia Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar degeneration Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar ataxia in diseases EC (disorder) Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Primary cerebellar degeneration NOS Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Other spinocerebellar diseases Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar disease NOS Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
[X]Other hereditary ataxias Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar ataxia NOS Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Progressive spinocerebellar ataxia with retained tendon reflexes (disorder) Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Vestibulocerebellar ataxia Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Nothnagel's syndrome Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebellar degeneration Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Sanger-Brown cerebellar ataxia Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia (disorder) Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Myoclonic epilepsy myopathy sensory ataxia (disorder) Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Complicated hereditary spastic paraplegia (disorder) Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
X-linked hereditary spastic paraplegia (disorder) Is a False Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pontocerebellar hypoplasia type 12 Is a True Spinocerebellar disease Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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