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770405003: Benign familial mesial temporal lobe epilepsy (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3700714010 Benign familial mesial temporal lobe epilepsy en Synonym Active Case insensitive SNOMED CT core
3700715011 Benign FMTLE (familial mesial temporal lobe epilepsy) en Synonym Active Initial character case insensitive SNOMED CT core
3700716012 Benign familial mesial temporal lobe epilepsy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3700717015 Rare epilepsy with characteristics of seizures with viscerosensory or experiential auras, onset in adolescence or early adulthood and good prognosis. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign familial mesial temporal lobe epilepsy Is a Temporal lobe epilepsy true Inferred relationship Some
Benign familial mesial temporal lobe epilepsy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Benign familial mesial temporal lobe epilepsy Is a Hereditary disorder of nervous system true Inferred relationship Some
Benign familial mesial temporal lobe epilepsy Finding site Temporal lobe structure 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

Description inactivation indicator reference set

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