86444004: Niemann-Pick disease, type C, acute form (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\...
• \Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
• \Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Disorder of foetus and/or newborn\Congenital disease\...
• \Inborn error of metabolism\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
• \Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Disorder of lysosomal enzyme\Lipid storage disease (disorder)\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
• \Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Enzymopathy\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Lipid storage disease (disorder)\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Lipoidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Lipid storage disease (disorder)\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type C (disorder)\Niemann-Pick disease, type C, acute form

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
143351017	Niemann-Pick disease, type C, acute form	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
828709011	Niemann-Pick disease, type C, acute form (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
143351017	Niemann-Pick disease, type C, acute form	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
828709011	Niemann-Pick disease, type C, acute form (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
828709011	Niemann-Pick disease, type C, acute form (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4672691000241111	maladie de Niemann-Pick type C aigue	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4672691000241111	maladie de Niemann-Pick type C aigue	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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