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230313001: Autosomal dominant late onset basal ganglia degeneration (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
345139014 Autosomal dominant late onset basal ganglia degeneration en Synonym Active Entire term case insensitive SNOMED CT core module
618103016 Autosomal dominant late onset basal ganglia degeneration (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2267591000000110 Neuroferritinopathy en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom Edition module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant late onset basal ganglia degeneration Is a Basal ganglia degeneration with calcification true Inferred relationship Existential restriction modifier
Autosomal dominant late onset basal ganglia degeneration Finding site Basal ganglion structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant late onset basal ganglia degeneration Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant late onset basal ganglia degeneration Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Autosomal dominant late onset basal ganglia degeneration Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant late onset basal ganglia degeneration Associated morphology Pathologic calcification, calcified structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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