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230387008: épilepsie occipitale bénigne à début précoce chez l'enfant (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2793363010 Panayiotopoulos syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
345236012 Benign occipital epilepsy of childhood - early onset variant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701676017 Benign childhood occipital epilepsy Panayiotopoulos type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3701677014 Early-onset benign childhood occipital epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618187017 Benign occipital epilepsy of childhood - early onset variant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
811861000241118 crise convulsive inaugurale de type Panayiotopoulos fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
832651000241117 épilepsie occipitale bénigne précoce de l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
832671000241110 syndrome de Panayiotopoulos fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
839211000241112 épilepsie occipitale bénigne à début précoce chez l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
839221000241117 épilepsie occipitale bénigne à début précoce chez l'enfant (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3701674019 A rare genetic neurological disorder characterised by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalised convulsion. Autonomic status epilepticus may be the only clinical event in some cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701675018 A rare genetic neurological disorder characterized by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalized convulsion. Autonomic status epilepticus may be the only clinical event in some cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign occipital epilepsy of childhood - early onset variant survenue (attribut) enfance false Inferred relationship Some
Benign occipital epilepsy of childhood - early onset variant est défini par la manifestation de (attribut) convulsion false Inferred relationship Some
Benign occipital epilepsy of childhood - early onset variant est un(e) (attribut) Childhood epilepsy with occipital paroxysms true Inferred relationship Some
Benign occipital epilepsy of childhood - early onset variant localisation d'une constatation (attribut) lobe occipital (structure corporelle) false Inferred relationship Some
Benign occipital epilepsy of childhood - early onset variant est défini par la manifestation de (attribut) Partial seizure false Inferred relationship Some
Benign occipital epilepsy of childhood - early onset variant est un(e) (attribut) Benign occipital lobe epilepsy (disorder) true Inferred relationship Some
Benign occipital epilepsy of childhood - early onset variant survenue (attribut) enfance true Inferred relationship Some 1
Benign occipital epilepsy of childhood - early onset variant localisation d'une constatation (attribut) lobe occipital (structure corporelle) true Inferred relationship Some 1
Benign occipital epilepsy of childhood - early onset variant est un(e) (attribut) Childhood seizure (finding) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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