784377008: Autosomal dominant epilepsy with auditory features (disorder)

\Finding of head region\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

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

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

4344461000052115 autosomalt dominant epilepsi med auditiva funktioner sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant epilepsy with auditory features (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant epilepsy with auditory features (disorder)	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Autosomal dominant epilepsy with auditory features (disorder)	Is a	Familial disease	true	Inferred relationship	Some
Autosomal dominant epilepsy with auditory features (disorder)	Is a	Temporal lobe epilepsy	true	Inferred relationship	Some
Autosomal dominant epilepsy with auditory features (disorder)	Finding site	Temporal lobe structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
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
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
4344461000052115	autosomalt dominant epilepsi med auditiva funktioner	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)