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715768000: Autosomal dominant dopa responsive dystonia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3303652013 Autosomal dominant dopa responsive dystonia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303653015 Autosomal dominant dopa responsive dystonia en Synonym Active Entire term case insensitive SNOMED CT core module
3303654014 Autosomal dominant Segawa syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3303655010 Hereditary progressive dystonia with marked diurnal fluctuation en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant dopa responsive dystonia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant dopa responsive dystonia Is a Diurnal dystonia true Inferred relationship Existential restriction modifier
Autosomal dominant dopa responsive dystonia Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant dopa responsive dystonia Finding site Extrapyramidal system structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant dopa responsive dystonia Interprets Movement true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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