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1231282002: Benign familial neonatal-infantile seizures (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Jun 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5072039016 Benign familial neonatal-infantile seizures (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5072040019 BFNIS - benign familial neonatal-infantile seizures en Synonym Active Entire term case sensitive SNOMED CT core module
5072041015 Benign neonatal-infantile epilepsy en Synonym Active Entire term case insensitive SNOMED CT core module
5072044011 Benign familial neonatal-infantile seizures en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign familial neonatal-infantile seizures Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Benign familial neonatal-infantile seizures Is a Partial seizure true Inferred relationship Existential restriction modifier
Benign familial neonatal-infantile seizures Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Benign familial neonatal-infantile seizures Is a Epilepsy true Inferred relationship Existential restriction modifier
Benign familial neonatal-infantile seizures Occurrence Infancy true Inferred relationship Existential restriction modifier 1
Benign familial neonatal-infantile seizures Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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