230389006: primaire hereditaire leesepilepsie (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Seizure\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Head finding (finding)\Finding of brain\Seizure\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

\Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy

\Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\...

\Combined focal and generalised epilepsy\Primary inherited reading epilepsy

\Reflex epilepsy\Primary inherited reading epilepsy

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Primary inherited reading epilepsy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Primary inherited reading epilepsy
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Primary inherited reading epilepsy
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Combined focal and generalised epilepsy\Primary inherited reading epilepsy
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\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
525271000146119 primaire erfelijke leesepilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
525281000146117 primaire erfelijke leesepilepsie (aandoening) nl Fully specified name Inactive Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
585041000146112 primaire hereditaire leesepilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8617861000146114 primaire hereditaire leesepilepsie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary inherited reading epilepsy	Is a	lokalisatiegebonden idiopathische epilepsie	false	Inferred relationship	Some
Primary inherited reading epilepsy	Finding site	Cerebrum	false	Inferred relationship	Some	1
Primary inherited reading epilepsy	Has definitional manifestation	Seizure	false	Inferred relationship	Some
Primary inherited reading epilepsy	Is a	Reflex epilepsy	true	Inferred relationship	Some
Primary inherited reading epilepsy	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Primary inherited reading epilepsy	Is a	Combined focal and generalised epilepsy	true	Inferred relationship	Some
Primary inherited reading epilepsy	Finding site	Brain structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets