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734021001: Spinocerebellar ataxia type 38 (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
3481925014 Spinocerebellar ataxia type 38 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481926010 Spinocerebellar ataxia type 38 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481927018 Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplopia and axonal neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4015951000052115 spinocerebellär ataxi, typ 38 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spinocerebellar ataxia type 38 (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia type 38 (disorder) Is a Hereditary cerebellar degeneration false Inferred relationship Some
Spinocerebellar ataxia type 38 (disorder) Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia type 38 (disorder) Associated morphology degeneration false Inferred relationship Some 2
Spinocerebellar ataxia type 38 (disorder) Finding site Cerebellar structure false Inferred relationship Some 2
Spinocerebellar ataxia type 38 (disorder) Associated morphology degeneration false Inferred relationship Some 3
Spinocerebellar ataxia type 38 (disorder) Finding site Spinal cord structure false Inferred relationship Some 3
Spinocerebellar ataxia type 38 (disorder) Finding site Cerebellar structure true Inferred relationship Some 1
Spinocerebellar ataxia type 38 (disorder) Finding site Spinal cord structure true Inferred relationship Some 2
Spinocerebellar ataxia type 38 (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Some 1
Spinocerebellar ataxia type 38 (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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