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784377008: Familial epilepsy with auditory features (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
3763854011 Autosomal dominant epilepsy with auditory features en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763855012 Autosomal dominant lateral temporal lobe epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5380923012 Familial epilepsy with auditory features en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5380924018 Familial epilepsy with auditory features (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5380925017 FEAF - familial epilepsy with auditory features en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763856013 A rare genetic familial partial epilepsy disease with characteristics of focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763852010 Partial epilepsy with auditory aura en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763853017 Autosomal dominant epilepsy with auditory features (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763854011 Autosomal dominant epilepsy with auditory features en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763855012 Autosomal dominant lateral temporal lobe epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5380923012 Familial epilepsy with auditory features en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5380924018 Familial epilepsy with auditory features (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5380925017 FEAF - familial epilepsy with auditory features en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763856013 A rare genetic familial partial epilepsy disease with characteristics of focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3396831001000119 Autosomal-dominante fokale Epilepsie mit akustischen Merkmalen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947201000241112 épilepsie autosomique dominante avec aura auditive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947201000241112 épilepsie autosomique dominante avec aura auditive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3396831001000119 Autosomal-dominante fokale Epilepsie mit akustischen Merkmalen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial epilepsy with auditory features Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial epilepsy with auditory features Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial epilepsy with auditory features Is a Familial disease false Inferred relationship Existential restriction modifier (core metadata concept)
Familial epilepsy with auditory features Is a Temporal lobe epilepsy false Inferred relationship Existential restriction modifier (core metadata concept)
Familial epilepsy with auditory features Finding site Temporal lobe structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial epilepsy with auditory features Is a Epilepsy with auditory features (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial epilepsy with auditory features Is a Familial temporal lobe epilepsy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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