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230437002: Severe myoclonic epilepsy in infancy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2006. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
345311015 Severe myoclonic epilepsy in infancy en Synonym Active Entire term case insensitive SNOMED CT core module
618244013 Severe myoclonic epilepsy in infancy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3513043019 Dravet Syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2193821000000118 Dravet syndrome en Synonym Inactive Entire term case sensitive SNOMED CT United Kingdom Edition module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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