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719208005: Spinocerebellar ataxia type 12 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3315420011 Spinocerebellar ataxia type 12 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3315421010 Spinocerebellar ataxia type 12 en Synonym Active Case insensitive SNOMED CT core
3315422015 Rare disease with manifestations of action tremor associated with relatively mild cerebellar ataxia. Associated pyramidal and extrapyramidal signs and dementia have been reported. Prevalence is unknown. Approximately 40 families have been reported. The pathogenesis seems to be related to a toxic effect at the RNA level as it is caused by a CAG expansion at the 5' end of the PPP2R2B gene on chromosome 5q31-5q32. 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 12 Finding site Spinal cord structure true Inferred relationship Some 1
Spinocerebellar ataxia type 12 Associated morphology Degenerative abnormality true Inferred relationship Some 2
Spinocerebellar ataxia type 12 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spinocerebellar ataxia type 12 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia type 12 Is a Hereditary cerebellar degeneration false Inferred relationship Some
Spinocerebellar ataxia type 12 Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia type 12 Associated morphology Degeneration false Inferred relationship Some 2
Spinocerebellar ataxia type 12 Associated morphology Degeneration false Inferred relationship Some 3
Spinocerebellar ataxia type 12 Finding site Cerebellar structure true Inferred relationship Some 2
Spinocerebellar ataxia type 12 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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