720864008: Encephalopathy due to prosaposin deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Finding of brain\Disorder of brain\Encephalopathy due to prosaposin deficiency
• \Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Encephalopathy due to prosaposin deficiency
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Disorder of brain\Encephalopathy due to prosaposin deficiency
• \Disorder of head\Disorder of brain\Encephalopathy due to prosaposin deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Encephalopathy due to prosaposin deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Encephalopathy due to prosaposin deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Encephalopathy due to prosaposin deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Encephalopathy due to prosaposin deficiency
• \Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Encephalopathy due to prosaposin deficiency
• \Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Encephalopathy due to prosaposin deficiency
• \Disease\Disorder of head\Disorder of brain\Encephalopathy due to prosaposin deficiency
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Encephalopathy due to prosaposin deficiency
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Sphingolipidosis\Encephalopathy due to prosaposin deficiency
• \Disease\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Encephalopathy due to prosaposin deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3322342017	Encephalopathy due to prosaposin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3322343010	Encephalopathy due to prosaposin deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3322344016	Combined prosaposin deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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