770623004: Benign occipital lobe epilepsy (disorder)

\Finding of head region\Occipital lobe epilepsy\Benign occipital lobe epilepsy (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

3701667012 Benign occipital epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3701669010 Benign occipital lobe epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3701670011 Benign occipital lobe epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3701668019 A rare genetic neurological disorder with characteristics of visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign occipital lobe epilepsy (disorder)	Finding site	Occipital lobe structure	true	Inferred relationship	Some	1
Benign occipital lobe epilepsy (disorder)	Is a	Occipital lobe epilepsy	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign occipital epilepsy of childhood - early onset variant	Is a	True	Benign occipital lobe epilepsy (disorder)	Inferred relationship	Some
Benign occipital epilepsy of childhood - late onset variant	Is a	True	Benign occipital lobe epilepsy (disorder)	Inferred relationship	Some

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
3701667012	Benign occipital epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3701669010	Benign occipital lobe epilepsy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3701670011	Benign occipital lobe epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3701668019	A rare genetic neurological disorder with characteristics of visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core