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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
196801000077117 maladie spinocérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
473131000077115 maladie spinocérébelleuse (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
834831014 Spinocerebellar disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


75 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spinocerebellar disease est un(e) (attribut) affection cérébelleuse true Inferred relationship Some
Spinocerebellar disease est un(e) (attribut) Encephalomyelopathy (disorder) true Inferred relationship Some
Spinocerebellar disease localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 2
Spinocerebellar disease est un(e) (attribut) Disorder of brain (disorder) false Inferred relationship Some
Spinocerebellar disease est un(e) (attribut) System disorder of the nervous system (disorder) false Inferred relationship Some
Spinocerebellar disease est un(e) (attribut) maladie dégénérative du système nerveux central false Inferred relationship Some
Spinocerebellar disease morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Spinocerebellar disease localisation d'une constatation (attribut) Structure of central nervous system (body structure) false Inferred relationship Some 2
Spinocerebellar disease localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Friedreich's ataxia est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
dégénérescence cérébelleuse sporadique est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Hereditary amblyopia with quadriplegia in the Irish Setter est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
paraplégie spastique héréditaire (trouble) est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Corticostriatal-spinal degeneration est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Progressive spinocerebellar ataxia with retained tendon reflexes est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Vestibulocerebellar ataxia est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Nothnagel's syndrome est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
syndrome de Roussy-Lévy (trouble) est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Hereditary cerebellar degeneration est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Sanger-Brown cerebellar ataxia est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Jervis' syndrome est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Athetosis with spastic paraplegia est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Bailey-Cushing syndrome (disorder) est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Paramyoclonus multiplex est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Ataxia-telangiectasia syndrome est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Primary progressive cerebellar degeneration est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Posthemiplegic ataxia est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Cerebellar degeneration est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
affection cérébelleuse est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Cerebellar ataxia associated with another disorder (disorder) est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
syndrome de déficience cérébelleuse est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Primary cerebellar degeneration NOS est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Other spinocerebellar diseases est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Spinocerebellar disease NOS est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
[X]Other hereditary ataxias est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Cerebellar ataxia NOS est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) est un(e) (attribut) True Spinocerebellar disease Inferred relationship Some
Complicated hereditary spastic paraplegia est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some
X-linked hereditary spastic paraplegia (disorder) est un(e) (attribut) False Spinocerebellar disease Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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