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1204415006: syndroom van autosomaal recessieve spinocerebellaire ataxie, blindheid en doofheid (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4955438013 SCAR3 - spinocerebellar ataxia autosomal recessive type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4955439017 Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4955440015 Autosomal recessive spinocerebellar ataxia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4955441016 Autosomal recessive spinocerebellar ataxia, blindness, hearing loss syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4955442011 Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
13607681000146117 syndroom van autosomaal recessieve spinocerebellaire ataxie, blindheid en doofheid (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13607691000146115 SCAR3 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13607701000146115 syndroom van autosomaal recessieve spinocerebellaire ataxie, blindheid en doofheid nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13607711000146118 autosomaal recessieve spinocerebellaire ataxie type 3 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13607721000146111 syndroom van autosomaal recessieve SCA, blindheid en doofheid nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
4955443018 A rare autosomal recessive syndromic cerebellar ataxia with the association of early-onset cerebellar ataxia, hearing loss and blindness. Patients may also present demyelinating peripheral motor neuropathy. Cerebral MRI shows alterations of the cerebellar white matter without cerebellar atrophy. 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
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Decreased hearing (finding) true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Blindness AND/OR vision impairment level true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Spinocerebellar ataxia true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Hearing loss associated with syndrome true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Finding site Structure of visual system (body structure) true Inferred relationship Some 4
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 5
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Interprets Hearing true Inferred relationship Some 3
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Has interpretation Decreased true Inferred relationship Some 3
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Finding site Cerebellar structure true Inferred relationship Some 1
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Finding site Spinal cord structure true Inferred relationship Some 2
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 2
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Is a Disorder of sensory function (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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