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


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
5035226012 AOA4 - ataxia, oculomotor apraxia type 4 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5035229017 Cerebellar ataxia with oculomotor apraxia type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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