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1217230002: Cerebellar ataxia with oculomotor apraxia type 4 (disorder)


Status: current, Primitive. Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5035225011 Cerebellar ataxia with oculomotor apraxia type 4 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5035226012 AOA4 - ataxia, oculomotor apraxia type 4 en Synonym Active Case sensitive SNOMED CT core
5035229017 Cerebellar ataxia with oculomotor apraxia type 4 en Synonym Active Case insensitive SNOMED CT core
5035228013 A rare autosomal recessive cerebellar ataxia with characteristics of onset of dystonia and other extrapyramidal signs, ataxia, oculomotor apraxia and progressive sensorimotor polyneuropathy in the first decade of life. Patients present distal muscle weakness and atrophy, decreased vibratory sensation and areflexia, and usually become wheelchair-bound by the third decade. Variable cognitive impairment may also be seen. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebellar ataxia with oculomotor apraxia type 4 Is a Dystonia true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Oculomotor apraxia true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Peripheral neuropathy true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Hereditary disorder of the visual system true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Hereditary ataxia true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Chronic brain syndrome true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Cerebellar ataxia true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 Clinical course Progressive true Inferred relationship Some 1
Cerebellar ataxia with oculomotor apraxia type 4 Interprets Movement true Inferred relationship Some 5
Cerebellar ataxia with oculomotor apraxia type 4 Finding site Cerebellar structure true Inferred relationship Some 2
Cerebellar ataxia with oculomotor apraxia type 4 Finding site Structure of visual system true Inferred relationship Some 3
Cerebellar ataxia with oculomotor apraxia type 4 Finding site Peripheral nerve structure true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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