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230232005: Late onset cerebellar ataxia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345043010 Late onset cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618014015 Late onset cerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
345043010 Late onset cerebellar ataxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345043010 Late onset cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618014015 Late onset cerebellar ataxia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618014015 Late onset cerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5931911000241112 ataxie cérébelleuse à début tardif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5931911000241112 ataxie cérébelleuse à début tardif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


19 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Late onset cerebellar ataxia Is a Cerebellar ataxia false Inferred relationship Existential restriction modifier (core metadata concept)
Late onset cerebellar ataxia Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Late onset cerebellar ataxia Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Late onset cerebellar ataxia Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Late onset cerebellar ataxia Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Late onset cerebellar ataxia Is a Ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Late onset cerebellar ataxia Is a Disease true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Progressive cerebellar ataxia Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Periodic ataxia Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Progressive spinocerebellar ataxia with decreased tendon reflexes Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Progressive spinocerebellar ataxia with retained tendon reflexes (disorder) Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Progressive cerebellar ataxia with palatal myoclonus (disorder) Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Progressive cerebellar ataxia with hypogonadism Is a False Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Olivopontocerebellar degeneration Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Azorean disease Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia Beauce type (disorder) Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic adult-onset ataxia of unknown aetiology Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)
A rare hereditary cerebellar ataxia disorder with characteristics of late-onset spinocerebellar ataxia, manifesting with slowly progressive gait disturbances, dysarthria, limb and truncal ataxia and smooth-pursuit eye movement disturbance, associated with a history of psychomotor delay from childhood. Mild atrophy of the cerebellar vermis and hemispheres is observed on brain imaging. There is evidence the disease is caused by homozygous mutation in the SYT14 gene on chromosome 1q32. Is a True Late onset cerebellar ataxia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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