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765091006: spinocerebellaire ataxie met axonale neuropathie type 1 (aandoening)


Status: current, Not 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
3656373011 Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3656374017 Spinocerebellar ataxia with axonal neuropathy type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6163301000146116 spinocerebellaire ataxie met axonale neuropathie type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6163311000146119 SCAN1 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6163321000146112 spinocerebellaire ataxie met axonale neuropathie type 1 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3656375016 A rare genetic neurological disorder characterised by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations in upper and lower extremities. Gaze nystagmus, cerebellar dysarthria, peripheral neuropathy, steppage gait and pes cavus develop as disease progresses. Cerebellar atrophy (especially of the vermis) is present in all affected individuals. Additional reported manifestations include seizures, mild brain atrophy, mild hypercholesterolaemia and borderline hypoalbuminaemia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3656376015 A rare genetic neurological disorder characterized by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations in upper and lower extremities. Gaze nystagmus, cerebellar dysarthria, peripheral neuropathy, steppage gait and pes cavus develop as disease progresses. Cerebellar atrophy (especially of the vermis) is present in all affected individuals. Additional reported manifestations include seizures, mild brain atrophy, mild hypercholesterolemia and borderline hypoalbuminemia. 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
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Associated morphology degeneratie (afwijkende morfologie) false Inferred relationship Some 2
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Finding site Cerebellar structure false Inferred relationship Some 2
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Associated morphology degeneratie (afwijkende morfologie) false Inferred relationship Some 1
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Finding site Spinal cord structure false Inferred relationship Some 1
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 2
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Finding site Spinal cord structure true Inferred relationship Some 2
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) Finding site Cerebellar structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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