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725392005: Autosomal dominant striatal neurodegeneration (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3441978014 Autosomal dominant striatal neurodegeneration (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3441979018 Autosomal dominant striatal neurodegeneration en Synonym Active Entire term case insensitive SNOMED CT core module
3441980015 ADSD - autosomal dominant striatal neurodegeneration en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant striatal neurodegeneration Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant striatal neurodegeneration Is a Parkinsonism true Inferred relationship Existential restriction modifier
Autosomal dominant striatal neurodegeneration Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Autosomal dominant striatal neurodegeneration Is a Cerebral degeneration true Inferred relationship Existential restriction modifier
Autosomal dominant striatal neurodegeneration Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal dominant striatal neurodegeneration Finding site Corpus striatum structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant striatal neurodegeneration Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant striatal neurodegeneration Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant striatal neurodegeneration Interprets Movement true Inferred relationship Existential restriction modifier 3
Autosomal dominant striatal neurodegeneration Has interpretation Slow true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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