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1208513005: Spinocerebellar ataxia type 42 (disorder)


Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4964981014 Spinocerebellar ataxia type 42 en Synonym Active Case insensitive SNOMED CT core
4964982019 Spinocerebellar ataxia type 42 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4964983012 A rare autosomal dominant cerebellar ataxia with characteristics of pure and slowly progressive cerebellar signs combining gait instability, dysarthria, nystagmus, saccadic eye movements and diplopia. Less frequent clinical signs and symptoms include spasticity, hyperreflexia, decreased distal vibration sense, urinary urgency or incontinence and postural tremor. 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 42 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia type 42 Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia type 42 Is a Chronic brain syndrome true Inferred relationship Some
Spinocerebellar ataxia type 42 Clinical course Progressive true Inferred relationship Some 3
Spinocerebellar ataxia type 42 Finding site Cerebellar structure true Inferred relationship Some 1
Spinocerebellar ataxia type 42 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spinocerebellar ataxia type 42 Finding site Spinal cord structure true Inferred relationship Some 2
Spinocerebellar ataxia type 42 Associated morphology Degenerative abnormality true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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