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785302009: Adult-onset autosomal recessive cerebellar ataxia (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3766843012 Adult-onset autosomal recessive cerebellar ataxia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3766844018 SCAR10 - autosomal recessive spinocerebellar ataxia type 10 en Synonym Active Case sensitive SNOMED CT core
3766845017 Adult-onset autosomal recessive cerebellar ataxia en Synonym Active Case insensitive SNOMED CT core
3766846016 Autosomal recessive spinocerebellar ataxia type 10 en Synonym Active Case insensitive SNOMED CT core
3766847013 A rare genetic autosomal recessive cerebellar ataxia disease with characteristics of adulthood-onset of slowly progressive spinocerebellar ataxia, manifesting with gait and appendicular ataxia, dysarthria, ocular movement anomalies (for example horizontal, vertical, and/or downbeat nystagmus, hypermetric saccades), increased deep tendon reflexes and progressive cognitive decline. Additional variable features may include proximal leg muscle wasting and fasciculations, pes cavus, inspiratory stridor, epilepsy, retinal degeneration and cataracts. Brain imaging reveals marked cerebellar atrophy and electromyography shows evidence of lower motor neuron involvement. Caused by homozygous or compound heterozygous mutation in the ANO10 gene on chromosome 3p22. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Adult-onset autosomal recessive cerebellar ataxia Occurrence Adulthood true Inferred relationship Some 1
Adult-onset autosomal recessive cerebellar ataxia Occurrence Adulthood true Inferred relationship Some 2
Adult-onset autosomal recessive cerebellar ataxia Finding site Spinal cord structure true Inferred relationship Some 2
Adult-onset autosomal recessive cerebellar ataxia Is a Chronic brain syndrome true Inferred relationship Some
Adult-onset autosomal recessive cerebellar ataxia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Adult-onset autosomal recessive cerebellar ataxia Associated morphology Degeneration false Inferred relationship Some 2
Adult-onset autosomal recessive cerebellar ataxia Associated morphology Degeneration false Inferred relationship Some 1
Adult-onset autosomal recessive cerebellar ataxia Is a Spinocerebellar ataxia true Inferred relationship Some
Adult-onset autosomal recessive cerebellar ataxia Finding site Cerebellar structure true Inferred relationship Some 1
Adult-onset autosomal recessive cerebellar ataxia Clinical course Progressive true Inferred relationship Some 3
Adult-onset autosomal recessive cerebellar ataxia Associated morphology Degenerative abnormality true Inferred relationship Some 2
Adult-onset autosomal recessive cerebellar ataxia Associated morphology Degenerative abnormality true Inferred relationship Some 1

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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