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

SNOMED CT Concept\Clinical 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\Disorder of lysosomal enzyme\Lipid storage disease\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 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\Neurological 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\Disorder of lysosomal enzyme\Lipid storage disease\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

\Congenital disease\Inborn error of metabolism\...

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

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

Status: current, Primitive. 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 Active Case sensitive SNOMED CT core

828709011 Niemann-Pick disease, type C, acute form (disorder) en Fully specified name Active Case sensitive 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	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set