230389006: Primary inherited reading epilepsy (disorder)

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

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

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

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

\Combined focal and generalized epilepsy (disorder)\Primary inherited reading epilepsy (disorder)

\Reflex epilepsy\Primary inherited reading epilepsy (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Primary inherited reading epilepsy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Primary inherited reading epilepsy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Primary inherited reading epilepsy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Combined focal and generalized epilepsy (disorder)\Primary inherited reading epilepsy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Combined focal and generalized epilepsy (disorder)\Primary inherited reading epilepsy (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Reflex epilepsy\Primary inherited reading epilepsy (disorder)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary inherited reading epilepsy (disorder)	Is a	epilessia idiopatica correlata a localizzazione	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary inherited reading epilepsy (disorder)	Finding site	The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary inherited reading epilepsy (disorder)	Has definitional manifestation	Seizure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary inherited reading epilepsy (disorder)	Is a	Reflex epilepsy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary inherited reading epilepsy (disorder)	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary inherited reading epilepsy (disorder)	Is a	Combined focal and generalized epilepsy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary inherited reading epilepsy (disorder)	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

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
345238013	Primary inherited reading epilepsy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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
4958701000241113	épilepsie primaire de lecture héritée	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4958701000241113	épilepsie primaire de lecture héritée	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module