703526007: Progressive epilepsy-intellectual disability syndrome Finnish type (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behavior and/or psychosocial function finding\Behavior finding\Intellectual disability\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipofuscinosis\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Degenerative disorder\Congenital degeneration of nervous system\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Degenerative disorder\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Disorder of body system\Disorder of nervous system\Chronic nervous system disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Congenital degeneration of nervous system\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipofuscinosis\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Metabolic disease\Chronic metabolic disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Lipofuscinosis\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipofuscinosis\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital degeneration of nervous system\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipofuscinosis\Neuronal ceroid lipofuscinosis\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Chronic disease\Chronic metabolic disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Chronic disease\Chronic nervous system disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Developmental disorder\Developmental hereditary disorder\Progressive epilepsy-intellectual disability syndrome Finnish type
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital degeneration of nervous system\Progressive epilepsy-intellectual disability syndrome Finnish type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3008925016	Progressive epilepsy with mental retardation	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3008996014	Northern epilepsy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3009778015	Neuronal ceroid lipofuscinosis 8	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3643140012	Progressive epilepsy-intellectual disability syndrome Finnish type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3643141011	Progressive epilepsy-intellectual disability syndrome Finnish type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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