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85102008: Cerebellar ataxia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
141095013 Cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141096014 Cerebellar ataxia, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
272311000077119 ataxie cérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
2966621018 Cerebellar ataxia (loss of muscle coordination) en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3397886017 Ataxie cérébelleuse fr Synonym (core metadata concept) Inactive Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
553321000077112 ataxie cérébelleuse (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
827086010 Cerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

133 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebellar ataxia est un(e) (attribut) maladie dégénérative du système nerveux central false Inferred relationship Some
Cerebellar ataxia est un(e) (attribut) lésion cérébrale false Inferred relationship Some
Cerebellar ataxia est un(e) (attribut) affection cérébelleuse true Inferred relationship Some
Cerebellar ataxia morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Cerebellar ataxia localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 1
Cerebellar ataxia est un(e) (attribut) Degenerative brain disorder false Inferred relationship Some
Cerebellar ataxia morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Cerebellar ataxia localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 1
Cerebellar ataxia est un(e) (attribut) Ataxia true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Gemignani syndrome (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Ataxia with tapetoretinal degeneration syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive spastic ataxia with leukoencephalopathy (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Infantile-onset autosomal recessive non progressive cerebellar ataxia est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Gillespie syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Saldino-Mainzer dysplasia est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
X-linked progressive cerebellar ataxia est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal dominant cerebellar ataxia type 2 est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Christianson syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia due to alcoholism est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
ataxie cérébelleuse aiguë causée par la varicelle est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Nothnagel's syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Sanger-Brown cerebellar ataxia est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Marie's cerebellar ataxia est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
Abortive cerebellar ataxia est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
Dyssynergia cerebellaris myoclonica est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia associated with another disorder (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Episodic ataxia (disorder) est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
Early onset cerebellar ataxia est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Late onset cerebellar ataxia est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
Drug-induced cerebellar ataxia est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia caused by toxin (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
ataxie cérébelleuse type Caïman est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
X-linked intellectual disability with ataxia and apraxia syndrome (disorder) est un(e) (attribut) False Cerebellar ataxia Inferred relationship Some
Ataxia with deafness and intellectual disability syndrome (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
ataxie cérébelleuse non progressive avec déficience intellectuelle est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive ataxia due to ubiquinone deficiency (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
syndrome d'ataxie cérébelleuse autosomique récessive-signes pyramidaux-nystagmus-apraxie oculomotrice est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with late-onset spasticity est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Olivopontocerebellar degeneration est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Dentatorubropallidoluysian degeneration est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Progressive spinocerebellar ataxia with retained tendon reflexes est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Fragile X associated tremor ataxia syndrome (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 7 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 6 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 4 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 3 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 5 (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia Beauce type (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
X-linked non progressive cerebellar ataxia (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Ataxia pancytopenia syndrome est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
CLCN2-related leukoencephalopathy est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) est un(e) (attribut) True Cerebellar ataxia Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

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

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

GB English

US English

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