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


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3766844018 SCAR10 - autosomal recessive spinocerebellar ataxia type 10 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3766845017 Adult-onset autosomal recessive cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3766846016 Autosomal recessive spinocerebellar ataxia type 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
3766843012 Adult-onset autosomal recessive cerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3766844018 SCAR10 - autosomal recessive spinocerebellar ataxia type 10 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3766845017 Adult-onset autosomal recessive cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3766846016 Autosomal recessive spinocerebellar ataxia type 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
3410471001000111 Autosomal-rezessive zerebelläre Ataxie mit Beginn im Erwachsenenalter de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5957491000241118 ataxie cérébelleuse autosomique récessive débutant à l'âge adulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5957491000241118 ataxie cérébelleuse autosomique récessive débutant à l'âge adulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3410471001000111 Autosomal-rezessive zerebelläre Ataxie mit Beginn im Erwachsenenalter de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Adult-onset autosomal recessive cerebellar ataxia (disorder) Occurrence Adulthood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult-onset autosomal recessive cerebellar ataxia (disorder) Occurrence Adulthood true Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult-onset autosomal recessive cerebellar ataxia (disorder) Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult-onset autosomal recessive cerebellar ataxia (disorder) Is a Chronic brain syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Adult-onset autosomal recessive cerebellar ataxia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Adult-onset autosomal recessive cerebellar ataxia (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult-onset autosomal recessive cerebellar ataxia (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult-onset autosomal recessive cerebellar ataxia (disorder) Is a Spinocerebellar ataxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Adult-onset autosomal recessive cerebellar ataxia (disorder) Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult-onset autosomal recessive cerebellar ataxia (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Adult-onset autosomal recessive cerebellar ataxia (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult-onset autosomal recessive cerebellar ataxia (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult-onset autosomal recessive cerebellar ataxia (disorder) Is a Chronic disorder of spinal cord (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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