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734021001: Spinocerebellar ataxia type 38 (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3481926010 Spinocerebellar ataxia type 38 en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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