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85102008: Cerebellar ataxia (disorder)

Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
141095013 Cerebellar ataxia en Synonym Active Case insensitive SNOMED CT core
141096014 Cerebellar ataxia, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
2966621018 Cerebellar ataxia (loss of muscle coordination) en Synonym Active Case insensitive SNOMED CT core
827086010 Cerebellar ataxia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

138 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebellar ataxia Is a Degenerative disease of the central nervous system false Inferred relationship Some
Cerebellar ataxia Is a Lesion of brain false Inferred relationship Some
Cerebellar ataxia Is a Cerebellar disorder true Inferred relationship Some
Cerebellar ataxia Associated morphology Degeneration false Inferred relationship Some 1
Cerebellar ataxia Finding site Cerebellar structure true Inferred relationship Some 1
Cerebellar ataxia Is a Degenerative brain disorder false Inferred relationship Some
Cerebellar ataxia Associated morphology Degeneration false Inferred relationship Some 1
Cerebellar ataxia Finding site Cerebellar structure false Inferred relationship Some 1
Cerebellar ataxia Is a 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 Is a True Cerebellar ataxia Inferred relationship Some
Gemignani syndrome Is a True Cerebellar ataxia Inferred relationship Some
Ataxia with tapetoretinal degeneration syndrome Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive spastic ataxia with leukoencephalopathy Is a True Cerebellar ataxia Inferred relationship Some
Infantile-onset autosomal recessive non progressive cerebellar ataxia Is a True Cerebellar ataxia Inferred relationship Some
Gillespie syndrome Is a True Cerebellar ataxia Inferred relationship Some
Saldino-Mainzer dysplasia Is a True Cerebellar ataxia Inferred relationship Some
X-linked progressive cerebellar ataxia Is a True Cerebellar ataxia Inferred relationship Some
Autosomal dominant cerebellar ataxia type 2 Is a True Cerebellar ataxia Inferred relationship Some
Christianson syndrome Is a True Cerebellar ataxia Inferred relationship Some
Congenital cerebellar ataxia due to RNU12 mutation Is a True Cerebellar ataxia Inferred relationship Some
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome Is a True Cerebellar ataxia Inferred relationship Some
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome Is a True Cerebellar ataxia Inferred relationship Some
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia due to alcoholism Is a False Cerebellar ataxia Inferred relationship Some
Acute cerebellar ataxia caused by varicella Is a True Cerebellar ataxia Inferred relationship Some
Nothnagel's syndrome Is a True Cerebellar ataxia Inferred relationship Some
Sanger-Brown cerebellar ataxia Is a True Cerebellar ataxia Inferred relationship Some
Marie's cerebellar ataxia Is a False Cerebellar ataxia Inferred relationship Some
Abortive cerebellar ataxia Is a False Cerebellar ataxia Inferred relationship Some
Dyssynergia cerebellaris myoclonica Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia associated with another disorder Is a True Cerebellar ataxia Inferred relationship Some
Episodic ataxia Is a False Cerebellar ataxia Inferred relationship Some
Early onset cerebellar ataxia Is a True Cerebellar ataxia Inferred relationship Some
Late onset cerebellar ataxia Is a False Cerebellar ataxia Inferred relationship Some
Drug-induced cerebellar ataxia Is a False Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia due to toxin Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 Is a True Cerebellar ataxia Inferred relationship Some
Boucher Neuhäuser syndrome Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia Cayman type Is a True Cerebellar ataxia Inferred relationship Some
X-linked intellectual disability with ataxia and apraxia syndrome Is a False Cerebellar ataxia Inferred relationship Some
Ataxia with deafness and intellectual disability syndrome Is a True Cerebellar ataxia Inferred relationship Some
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome Is a True Cerebellar ataxia Inferred relationship Some
Non-progressive cerebellar ataxia with intellectual disability Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive ataxia due to ubiquinone deficiency Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 Is a True Cerebellar ataxia Inferred relationship Some
Myoclonus, cerebellar ataxia, deafness syndrome Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome Is a True Cerebellar ataxia Inferred relationship Some
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with late-onset spasticity Is a True Cerebellar ataxia Inferred relationship Some
Olivopontocerebellar degeneration Is a True Cerebellar ataxia Inferred relationship Some
Dentatorubropallidoluysian degeneration Is a True Cerebellar ataxia Inferred relationship Some
Spinocerebellar ataxia Is a True Cerebellar ataxia Inferred relationship Some
Progressive spinocerebellar ataxia with retained tendon reflexes Is a True Cerebellar ataxia Inferred relationship Some
Fragile X associated tremor ataxia syndrome Is a True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 7 Is a True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 6 Is a True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 4 Is a True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 3 Is a True Cerebellar ataxia Inferred relationship Some
Episodic ataxia type 5 Is a True Cerebellar ataxia Inferred relationship Some
Hypomyelinating leucodystrophy with atrophy of basal ganglia and cerebellum Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia Beauce type Is a True Cerebellar ataxia Inferred relationship Some
Sporadic adult-onset ataxia of unknown aetiology Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome Is a True Cerebellar ataxia Inferred relationship Some
X-linked non progressive cerebellar ataxia Is a True Cerebellar ataxia Inferred relationship Some
Ataxia pancytopenia syndrome Is a True Cerebellar ataxia Inferred relationship Some
CLCN2-related leukoencephalopathy Is a True Cerebellar ataxia Inferred relationship Some
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency Is a True Cerebellar ataxia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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