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715827001: dystonie dopa-sensible autosomique récessive (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
3303839018 Autosomal recessive dopa responsive dystonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303840016 Autosomal recessive dopa responsive dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303841017 Autosomal recessive Segawa syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303842012 Tyrosine hydroxylase deficient dopa responsive dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4554514017 Tyrosine hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
748731000241118 dystonie dopa-sensible autosomique récessive (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
918181000172113 dystonie dopa-sensible autosomique récessive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
977781000172115 DYT5b - dystonie dopa-sensible autosomique récessive fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303843019 Autosomal recessive dopa responsive dystonia (DYT5b) is a very rare neurometabolic disorder with a spectrum of symptoms ranging from those seen in dopa responsive dystonia to progressive infantile encephalopathy. Disease presents in infancy (most frequently in the first year of life) with a progressive hypokinetic rigid syndrome, involuntary jerky movements, postural tremor, or gait disturbances that may fluctuate during the day and show good or excellent responsiveness to levodopa in most cases. DYT5b is caused by mutations in the tyrosine hydroxylase TH gene (11p15.5). Inherited in an autosomal recessive manner. 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 dopa responsive dystonia (disorder) interprète (attribut) Movement (observable entity) true Inferred relationship Some 2
Autosomal recessive dopa responsive dystonia (disorder) est un(e) (attribut) Autosomal recessive idiopathic familial dystonia true Inferred relationship Some
Autosomal recessive dopa responsive dystonia (disorder) est un(e) (attribut) Diurnal dystonia true Inferred relationship Some
Autosomal recessive dopa responsive dystonia (disorder) localisation d'une constatation (attribut) Extrapyramidal system structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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