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718770005: Spinocerebellar ataxia type 25 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3313798011 Spinocerebellar ataxia type 25 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313799015 Spinocerebellar ataxia type 25 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401869018 Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia. It is characterized by cerebellar ataxia and prominent sensory neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401870017 Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia. It is characterised by cerebellar ataxia and prominent sensory neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313798011 Spinocerebellar ataxia type 25 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313798011 Spinocerebellar ataxia type 25 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313799015 Spinocerebellar ataxia type 25 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313799015 Spinocerebellar ataxia type 25 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313800016 A very rare subtype of type I autosomal dominant cerebellar ataxia with characteristics of cerebellar ataxia and prominent sensory neuropathy. Fewer than 10 cases in a 4-generation French family have been reported to date. Age of onset ranges from 1 to 39 years. The clinical features vary widely from sensory neuropathy with little cerebellar ataxia to cerebellar ataxia with little sensory neuropathy. Some patients exhibit gastrointestinal disorders such as vomiting and abdominal pain as initial symptoms. Scoliosis and urinary problems are also observed. Maps to chromosome 2p15-p21. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401869018 Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia. It is characterized by cerebellar ataxia and prominent sensory neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401870017 Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia. It is characterised by cerebellar ataxia and prominent sensory neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3448101001000115 Ataxie, spinozerebelläre, Typ 25 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
950251000172119 SCA25 - spinocerebellar ataxia type 25 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
969461000172117 ataxie spinocérébelleuse type 25 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
950251000172119 SCA25 - spinocerebellar ataxia type 25 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
969461000172117 ataxie spinocérébelleuse type 25 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3448101001000115 Ataxie, spinozerebelläre, Typ 25 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
Spinocerebellar ataxia type 25 (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 25 (disorder) Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 25 (disorder) Is a Spinocerebellar ataxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 25 (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spinocerebellar ataxia type 25 (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 3
Spinocerebellar ataxia type 25 (disorder) Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spinocerebellar ataxia type 25 (disorder) Finding site Spinal cord structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Spinocerebellar ataxia type 25 (disorder) Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spinocerebellar ataxia type 25 (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spinocerebellar ataxia type 25 (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) 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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