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734023003: Sporadic adult-onset ataxia of unknown etiology (disorder)


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
5403869011 A rare non-hereditary degenerative ataxia disease characterized by a 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
5403870012 A rare non-hereditary degenerative ataxia disease characterised by a 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
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
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
5403869011 A rare non-hereditary degenerative ataxia disease characterized by a 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
5403870012 A rare non-hereditary degenerative ataxia disease characterised by a 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
3408901001000114 Sporadische Ataxie unbekannter Ätiologie im Erwachsenenalter de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
892701000172113 ataxie sporadique tardive d'étiologie indéterminée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
921871000172115 ataxie sporadique de l'adulte d'étiologie indéterminée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
892701000172113 ataxie sporadique tardive d'étiologie indéterminée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
921871000172115 ataxie sporadique de l'adulte d'étiologie indéterminée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3408901001000114 Sporadische Ataxie unbekannter Ätiologie im Erwachsenenalter de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sporadic adult-onset ataxia of unknown aetiology Is a Ataxia false Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic adult-onset ataxia of unknown aetiology Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic adult-onset ataxia of unknown aetiology Is a Late onset cerebellar ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic adult-onset ataxia of unknown aetiology Is a Degenerative disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic adult-onset ataxia of unknown aetiology Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic adult-onset ataxia of unknown aetiology Occurrence Adulthood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic adult-onset ataxia of unknown aetiology Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic adult-onset ataxia of unknown aetiology Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic adult-onset ataxia of unknown aetiology Is a Cerebellar degeneration true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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