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724227000: Infantile onset spinocerebellar ataxia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3432877015 Infantile onset spinocerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3432878013 Infantile onset spinocerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3432879017 Ohaha syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3432880019 Ophthalmoplegia, hypotonia, ataxia, hypoacusis, athetosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403283019 Infantile-onset spinocerebellar ataxia (IOSCA) is a hereditary neurological disorder with early and severe involvement of both the peripheral and central nervous systems. It has only been described in Finnish families. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3432877015 Infantile onset spinocerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3432878013 Infantile onset spinocerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3432879017 Ohaha syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3432880019 Ophthalmoplegia, hypotonia, ataxia, hypoacusis, athetosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3432881015 A hereditary neurological disorder with early and severe involvement of both the peripheral and central nervous systems. It has only been described in Finnish families. Some patients show intellectual deficit. Epilepsy is a late manifestation and seizures may be life threatening. Caused by mutations in the C10orf2 gene (10q24) encoding the mitochondrial helicase Twinkle. The c.1523A>G (p.Y508C) causative mutation has been postulated to be a founder mutation. The mutations lead to mtDNA depletion in the brain and the liver but not in the muscle. Inherited in an autosomal recessive manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403283019 Infantile-onset spinocerebellar ataxia (IOSCA) is a hereditary neurological disorder with early and severe involvement of both the peripheral and central nervous systems. It has only been described in Finnish families. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3452331001000114 Ataxie, infantile spinozerebelläre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
876681000172115 ataxie spinocérébelleuse infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
930261000172118 syndrome Ohaha (ophtalmoplégie, hypotonie, ataxie, hypoacousie, athétose) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
876681000172115 ataxie spinocérébelleuse infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
930261000172118 syndrome Ohaha (ophtalmoplégie, hypotonie, ataxie, hypoacousie, athétose) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3452331001000114 Ataxie, infantile spinozerebelläre 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
Infantile onset spinocerebellar ataxia (disorder) Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile onset spinocerebellar ataxia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile onset spinocerebellar ataxia (disorder) Is a Spinocerebellar ataxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile onset spinocerebellar ataxia (disorder) Is a Mitochondrial cytopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile onset spinocerebellar ataxia (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 3
Infantile onset spinocerebellar ataxia (disorder) Occurrence Infancy false Inferred relationship Existential restriction modifier (core metadata concept) 3
Infantile onset spinocerebellar ataxia (disorder) Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Infantile onset spinocerebellar ataxia (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 4
Infantile onset spinocerebellar ataxia (disorder) Occurrence Infancy false Inferred relationship Existential restriction modifier (core metadata concept) 4
Infantile onset spinocerebellar ataxia (disorder) Finding site Spinal cord structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Infantile onset spinocerebellar ataxia (disorder) Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile onset spinocerebellar ataxia (disorder) Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Infantile onset spinocerebellar ataxia (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Infantile onset spinocerebellar ataxia (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile onset spinocerebellar ataxia (disorder) Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Infantile onset spinocerebellar ataxia (disorder) Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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