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719302009: Spinocerebellar ataxia type 5 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3315917014 Spinocerebellar ataxia type 5 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3315918016 Spinocerebellar ataxia type 5 en Synonym Active Case insensitive SNOMED CT core
3315919012 Disease with characteristics of early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.Three families have been reported to date. Clinical manifestations include cerebellar signs (ataxia, dysarthria, and intention tremor) and eye movement abnormalities such as gaze-evoked nystagmus, down beat nystagmus, and impaired smooth pursuit. Occasionally defects of the visual field and horizontal gaze palsy can be also present. Non-cerebellar signs such as facial myokymia, resting tremor, writer's cramp, impaired vibration sense and brisk deep tendon reflexes have been reported in some patients. Caused by mutations in the SPTBN2 gene (11q13.2) encoding beta-III spectrin, a protein essential for the correct functioning and development of Purkinje cells. Inherited autosomal dominantly. 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 5 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spinocerebellar ataxia type 5 Associated morphology Degenerative abnormality true Inferred relationship Some 2
Spinocerebellar ataxia type 5 Finding site Spinal cord structure true Inferred relationship Some 1
Spinocerebellar ataxia type 5 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia type 5 Is a Hereditary cerebellar degeneration false Inferred relationship Some
Spinocerebellar ataxia type 5 Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia type 5 Associated morphology Degeneration false Inferred relationship Some 2
Spinocerebellar ataxia type 5 Associated morphology Degeneration false Inferred relationship Some 3
Spinocerebellar ataxia type 5 Finding site Cerebellar structure true Inferred relationship Some 2
Spinocerebellar ataxia type 5 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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