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734023003: ataxie sporadique tardive d'étiologie indéterminée (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3481956018 Sporadic adult-onset ataxia of unknown etiology (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481957010 Sporadic adult-onset ataxia of unknown etiology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481958017 Sporadic adult-onset ataxia of unknown aetiology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481959013 Idiopathic late-onset cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481960015 Sporadic adult-onset ataxia of unknown origin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
763571000241114 ataxie sporadique tardive d'étiologie indéterminée (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
892701000172113 ataxie sporadique tardive d'étiologie indéterminée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
921871000172115 ataxie sporadique de l'adulte d'étiologie indéterminée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3481961016 Non-hereditary degenerative ataxia with characteristics of slowly progressive cerebellar syndrome (with ataxia of stance and gait, upper limb dysmetria and intention tremor, ataxic speech, and oculomotor abnormalities), presenting in adulthood (at around 50 years of age), that is not due to a known cause. Extracerebellar symptoms (e.g., decreased vibration sense and absent or decreased ankle reflexes), polyneuropathy and mild autonomic dysfunction may also be present. Mild cognitive impairment has also rarely been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) Cerebellar degeneration true Inferred relationship Some
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) Ataxia false Inferred relationship Some
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) maladie idiopathique true Inferred relationship Some
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) Late onset cerebellar ataxia true Inferred relationship Some
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) affection dégénérative false Inferred relationship Some
Sporadic adult-onset ataxia of unknown etiology (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Sporadic adult-onset ataxia of unknown etiology (disorder) survenue (attribut) Adulthood (qualifier value) true Inferred relationship Some 1
Sporadic adult-onset ataxia of unknown etiology (disorder) localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 1
Sporadic adult-onset ataxia of unknown etiology (disorder) est un(e) (attribut) Cerebellar ataxia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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