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715825009: ataxie spinocérébelleuse type 29 (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1012291000172114 ataxie spinocérébelleuse type 29 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303832010 Spinocerebellar ataxia type 29 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303833017 Spinocerebellar ataxia type 29 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303834011 Congenital nonprogressive spinocerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
748711000241110 ataxie spinocérébelleuse type 29 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
947961000172112 ataxie spinocérébelleuse non progressive congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303835012 Spinocerebellar ataxia type 29 (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manifestations of very slowly progressive or non-progressive gait and limb ataxia causing delayed walking and frequent falling in children. Mild developmental delay, learning difficulties, and language dysfunction are frequently reported. Other manifestations include nystagmus, dysarthria, dysmetria, and dysdiadochokinesia. SCA29 is due to mutations in the ITPR1 gene (3p26.1), which is equally the causal gene of SCA15. Inherited autosomal dominantly. 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
ataxie spinocérébelleuse type 29 localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
ataxie spinocérébelleuse type 29 localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 2
ataxie spinocérébelleuse type 29 morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 2
ataxie spinocérébelleuse type 29 morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
ataxie spinocérébelleuse type 29 est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
ataxie spinocérébelleuse type 29 est un(e) (attribut) Hereditary cerebellar degeneration false Inferred relationship Some
ataxie spinocérébelleuse type 29 est un(e) (attribut) ataxie spinocérébelleuse dominante true Inferred relationship Some
ataxie spinocérébelleuse type 29 morphologie associée (attribut) dégénérescence false Inferred relationship Some 2
ataxie spinocérébelleuse type 29 localisation d'une constatation (attribut) moelle spinale (structure corporelle) false Inferred relationship Some 2
ataxie spinocérébelleuse type 29 morphologie associée (attribut) dégénérescence false Inferred relationship Some 3
ataxie spinocérébelleuse type 29 localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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