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230422001: Myoclonic absence epilepsy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345287010 Epilepsy with myoclonic absences en Synonym Active Case insensitive SNOMED CT core
345288017 Myoclonic absence epilepsy en Synonym Active Case insensitive SNOMED CT core
618227014 Myoclonic absence epilepsy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myoclonic absence epilepsy Is a Absence seizure false Inferred relationship Some
Myoclonic absence epilepsy Is a Generalised epilepsy true Inferred relationship Some
Myoclonic absence epilepsy Is a Myoclonic absence seizure true Inferred relationship Some
Myoclonic absence epilepsy Has definitional manifestation Seizure false Inferred relationship Some
Myoclonic absence epilepsy Is a Cryptogenic generalised epilepsy false Inferred relationship Some
Myoclonic absence epilepsy Finding site Structure of cerebrum true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Perioral myoclonia with absences Is a True Myoclonic absence epilepsy Inferred relationship Some

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Queensland allied health indicator for intervention reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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