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192990004: Benign myoclonic epilepsy in infancy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
297280011 Benign myoclonic epilepsy in infancy en Synonym Active Case insensitive SNOMED CT core
297281010 Neonatal myoclonic epilepsy en Synonym Active Case insensitive SNOMED CT core
576829014 Benign myoclonic epilepsy in infancy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign myoclonic epilepsy in infancy Is a Idiopathic generalised epilepsy true Inferred relationship Some
Benign myoclonic epilepsy in infancy Has definitional manifestation Seizure false Inferred relationship Some
Benign myoclonic epilepsy in infancy Finding site Structure of cerebrum true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

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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