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715827001: Autosomal recessive 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
3303839018 Autosomal recessive dopa responsive dystonia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303840016 Autosomal recessive dopa responsive dystonia en Synonym Active Entire term case insensitive SNOMED CT core module
3303841017 Autosomal recessive Segawa syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3303842012 Tyrosine hydroxylase deficient dopa responsive dystonia en Synonym Active Entire term case insensitive SNOMED CT core module
4554514017 Tyrosine hydroxylase deficiency 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 recessive dopa responsive dystonia Is a Autosomal recessive idiopathic familial dystonia true Inferred relationship Existential restriction modifier
Autosomal recessive dopa responsive dystonia Is a Diurnal dystonia true Inferred relationship Existential restriction modifier
Autosomal recessive dopa responsive dystonia Finding site Extrapyramidal system structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive 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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