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\Niemann-Pick disease, type C\Niemann-Pick disease, type C, acute form

\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type C\Niemann-Pick disease, type C, acute form

\Disorder of foetus and/or newborn\Congenital disease (disorder)\...

\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\Niemann-Pick disease, type C\Niemann-Pick disease, type C, acute form

\Disorder of lysosomal enzyme\Lipid storage disease\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type C\Niemann-Pick disease, type C, acute form

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Niemann-Pick disease, type C, acute form
\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\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\Niemann-Pick disease, type C\Niemann-Pick disease, type C, acute form
\Metabolic disease\Enzymopathy\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type C\Niemann-Pick disease, type C, acute form
\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Lipid storage disease\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type C\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\Niemann-Pick disease, type C\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\Niemann-Pick disease, type C\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\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type C\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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Niemann-Pick disease, type C, acute form	Is a	Inherited metabolic disorder of nervous system	true	Inferred relationship	Some
Niemann-Pick disease, type C, acute form	Is a	Niemann-Pick disease, type C	true	Inferred relationship	Some
Niemann-Pick disease, type C, acute form	Occurrence	Congenital	true	Inferred relationship	Some	1
Niemann-Pick disease, type C, acute form	Associated morphology	Niemann-Pick cell	false	Inferred relationship	Some
Niemann-Pick disease, type C, acute form	Associated morphology	Foam cell	false	Inferred relationship	Some
Niemann-Pick disease, type C, acute form	Finding site	Structure of nervous system (body structure)	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets