771223000: Infantile epileptic dyskinetic encephalopathy (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy

\Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Central nervous system finding\Finding of brain\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy

\Finding of head and neck region\Head finding\...

\Finding of brain\Seizure\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Finding of brain\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Finding of brain\Disorder of brain\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy

\Disorder of head\Disorder of brain\...

\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy

\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy

\Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Infantile epileptic dyskinetic encephalopathy
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Infantile epileptic dyskinetic encephalopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Infantile epileptic dyskinetic encephalopathy
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Infantile epileptic dyskinetic encephalopathy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy
\Disease\Disorder of head\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy\Epileptic encephalopathy\Infantile epileptic dyskinetic encephalopathy
\Disease\Disorder of head\Disorder of brain\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Infantile epileptic dyskinetic encephalopathy

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3705165013 Infantile epileptic dyskinetic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3705166014 Infantile epileptic dyskinetic encephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Infantile epileptic dyskinetic encephalopathy	Finding site	Extrapyramidal system structure	true	Inferred relationship	Existential restriction modifier	1
Infantile epileptic dyskinetic encephalopathy	Is a	Dystonia	true	Inferred relationship	Existential restriction modifier
Infantile epileptic dyskinetic encephalopathy	Is a	X-linked hereditary disease	false	Inferred relationship	Existential restriction modifier
Infantile epileptic dyskinetic encephalopathy	Finding site	Structure of cerebrum	true	Inferred relationship	Existential restriction modifier	2
Infantile epileptic dyskinetic encephalopathy	Is a	Epileptic encephalopathy	true	Inferred relationship	Existential restriction modifier
Infantile epileptic dyskinetic encephalopathy	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Infantile epileptic dyskinetic encephalopathy	Interprets	Movement	true	Inferred relationship	Existential restriction modifier	3
Infantile epileptic dyskinetic encephalopathy	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

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Active

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Characteristic

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This concept is not in any reference sets