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702421006: Familial encephalopathy with neuroserpin inclusion bodies (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3009273013 Familial encephalopathy with neuroserpin inclusion bodies en Synonym Active Entire term case insensitive SNOMED CT core module
3009514013 Familial encephalopathy with neuroserpin inclusion bodies (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3009601017 Familial dementia with neuroserpin inclusion bodies 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
Familial encephalopathy with neuroserpin inclusion bodies Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial encephalopathy with neuroserpin inclusion bodies Is a Disorder of brain true Inferred relationship Existential restriction modifier
Familial encephalopathy with neuroserpin inclusion bodies Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Familial encephalopathy with neuroserpin inclusion bodies Finding site Brain 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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