18927009: Niemann-Pick disease, type D (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D

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

\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D

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

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D
\Metabolic disease\Enzymopathy\Lysosomal storage disease (disorder)\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D
\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Lipid storage disease\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Lipoidosis\Sphingomyelin/cholesterol lipidosis\Niemann-Pick disease, type D
\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 D

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

31905016 Niemann-Pick disease, type D en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

31906015 Niemann-Pick disease, Nova Scotian en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

746553016 Niemann-Pick disease, type D (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

1222212015 Niemann-Pick disease type D en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3038211012 Niemann pick disease type D en Synonym (core metadata concept) 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 D	Is a	Sphingomyelin/cholesterol lipidosis	true	Inferred relationship	Some
Niemann-Pick disease, type D	Associated morphology	Niemann-Pick cell	false	Inferred relationship	Some
Niemann-Pick disease, type D	Finding site	Body system structure	false	Inferred relationship	Some
Niemann-Pick disease, type D	Associated morphology	Foam cell	false	Inferred relationship	Some
Niemann-Pick disease, type D	Occurrence	Congenital	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets