230389006: Primary inherited reading epilepsy (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du système nerveux central\constatation à propos l'encéphale\convulsion\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\constatation à propos l'encéphale\convulsion\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\constatation à propos l'encéphale\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

\affection de la tête\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

\Neurological finding\Seizure related finding\convulsion\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Primary inherited reading epilepsy
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Primary inherited reading epilepsy
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Primary inherited reading epilepsy
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\Disease\affection de la tête\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

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

345238013 Primary inherited reading epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618190011 Primary inherited reading epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary inherited reading epilepsy	est un(e) (attribut)	Reflex epilepsy	true	Inferred relationship	Some
Primary inherited reading epilepsy	est un(e) (attribut)	Hereditary disorder of nervous system	true	Inferred relationship	Some
Primary inherited reading epilepsy	est défini par la manifestation de (attribut)	convulsion	false	Inferred relationship	Some
Primary inherited reading epilepsy	est un(e) (attribut)	Localisation-related idiopathic epilepsy	false	Inferred relationship	Some
Primary inherited reading epilepsy	localisation d'une constatation (attribut)	structure du cerveau	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Canada English language reference set (foundation metadata concept)

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

Description inactivation indicator reference set