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230422001: Myoclonic absence epilepsy (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
345287010 Epilepsy with myoclonic absences en Synonym Active Entire term case insensitive SNOMED CT core module
345288017 Myoclonic absence epilepsy en Synonym Active Entire term case insensitive SNOMED CT core module
618227014 Myoclonic absence epilepsy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myoclonic absence epilepsy Is a Cryptogenic generalized epilepsy false Inferred relationship Existential restriction modifier
Myoclonic absence epilepsy Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Myoclonic absence epilepsy Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier
Myoclonic absence epilepsy Is a Absence seizure false Inferred relationship Existential restriction modifier
Myoclonic absence epilepsy Is a Generalized epilepsy true Inferred relationship Existential restriction modifier
Myoclonic absence epilepsy Is a Myoclonic absence seizure true Inferred relationship Existential restriction modifier

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

This concept is not in any reference sets

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