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230437002: Severe myoclonic epilepsy in infancy (disorder)


Status: current, Primitive. Date: 31-Jul 2006. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345311015 Severe myoclonic epilepsy in infancy en Synonym Active Case insensitive SNOMED CT core
3513043019 Dravet Syndrome en Synonym Active Case sensitive SNOMED CT core
618244013 Severe myoclonic epilepsy in infancy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3513044013 A genetic epilepsy of childhood with characteristics of drug-resistant seizures often induced by fever, presenting in previously healthy children, and which frequently leads to cognitive and motor impairment. Seizures can regress in adulthood but most patients have ongoing seizures that are refractory to medication. Around 85% of cases are due to a mutation or deletion in the SCN1A gene (2q24.3), encoding a voltage-gated sodium channel essential for the excitability of neurons. In families with a known SCN1A mutation, inheritance is autosomal dominant. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe myoclonic epilepsy in infancy Interprets Movement false Inferred relationship Some 2
Severe myoclonic epilepsy in infancy Is a Myoclonic epilepsy of early childhood false Inferred relationship Some
Severe myoclonic epilepsy in infancy Occurrence Childhood false Inferred relationship Some
Severe myoclonic epilepsy in infancy Occurrence Infancy false Inferred relationship Some
Severe myoclonic epilepsy in infancy Has definitional manifestation Seizure false Inferred relationship Some
Severe myoclonic epilepsy in infancy Is a Epilepsy undetermined whether focal or generalised false Inferred relationship Some
Severe myoclonic epilepsy in infancy Severity Severe false Inferred relationship Some
Severe myoclonic epilepsy in infancy Finding site Structure of cerebrum false Inferred relationship Some
Severe myoclonic epilepsy in infancy Is a Refractory myoclonic epilepsy true Inferred relationship Some
Severe myoclonic epilepsy in infancy Is a Epileptic encephalopathy true Inferred relationship Some
Severe myoclonic epilepsy in infancy Occurrence Infancy true Inferred relationship Some 1
Severe 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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