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734020000: Spinocerebellar ataxia type 40 (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3481917012 Spinocerebellar ataxia type 40 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3481918019 Spinocerebellar ataxia type 40 en Synonym Active Case insensitive SNOMED CT core
3481919010 A very rare disease with characteristics of adult-onset unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria, intention tremor, scanning speech, hyperreflexia and dysdiadochokinesis. 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 40 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spinocerebellar ataxia type 40 Associated morphology Degenerative abnormality true Inferred relationship Some 2
Spinocerebellar ataxia type 40 Finding site Cerebellar structure true Inferred relationship Some 1
Spinocerebellar ataxia type 40 Finding site Spinal cord structure true Inferred relationship Some 2
Spinocerebellar ataxia type 40 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia type 40 Is a Hereditary cerebellar degeneration false Inferred relationship Some
Spinocerebellar ataxia type 40 Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia type 40 Associated morphology Degeneration false Inferred relationship Some 2
Spinocerebellar ataxia type 40 Finding site Cerebellar structure false Inferred relationship Some 2
Spinocerebellar ataxia type 40 Associated morphology Degeneration false Inferred relationship Some 3
Spinocerebellar ataxia type 40 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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