FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

702421006: Familial encephalopathy with neuroserpin inclusion bodies (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3009273013 Familial encephalopathy with neuroserpin inclusion bodies en Synonym Active Case insensitive SNOMED CT core
3009514013 Familial encephalopathy with neuroserpin inclusion bodies (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3009601017 Familial dementia with neuroserpin inclusion bodies en Synonym Active Case insensitive SNOMED CT core


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 Some
Familial encephalopathy with neuroserpin inclusion bodies Is a Encephalopathy true Inferred relationship Some
Familial encephalopathy with neuroserpin inclusion bodies Is a Hereditary disorder of nervous system true Inferred relationship Some
Familial encephalopathy with neuroserpin inclusion bodies Finding site Brain structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start