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783739005: Familial temporal lobe epilepsy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3760106019 Familial temporal lobe epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3760107011 Familial temporal lobe epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3760108018 Rare genetic epilepsy with characteristics of mostly benign simple or complex partial seizures with autonomic or psychic auras. Seizures occur infrequently, are of short duration and are usually well controlled with medication. Development and cognition are normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial temporal lobe epilepsy (disorder) Is a Familial disease true Inferred relationship Some
Familial temporal lobe epilepsy (disorder) Is a Genetic disease true Inferred relationship Some
Familial temporal lobe epilepsy (disorder) Is a Temporal lobe epilepsy true Inferred relationship Some
Familial temporal lobe epilepsy (disorder) Finding site Temporal lobe structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial mesial temporal lobe epilepsy Is a True Familial temporal lobe epilepsy (disorder) Inferred relationship Some
Familial epilepsy with auditory features Is a True Familial temporal lobe epilepsy (disorder) Inferred relationship Some

This concept is not in any reference sets

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