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

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\...

\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\maladie de surchage lipidique\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type D

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

\trouble métabolique\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\maladie de surchage lipidique\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type D
\trouble métabolique\Enzymopathy\Disorder of lysosomal enzyme\maladie de surchage lipidique\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type D
\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\Disorder of lipid storage and metabolism\Sphingolipidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type D
\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\Disorder of lipid storage and metabolism\Lipoidosis\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type D
\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\Disorder of lipid storage and metabolism\maladie de surchage lipidique\Sphingomyelin/cholesterol lipidosis (disorder)\Niemann-Pick disease, type D

\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\maladie de surchage lipidique\Sphingomyelin/cholesterol lipidosis (disorder)\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

1007251000172119 maladie de Niemann-Pick type Nova Scotian fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

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

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

402351000241113 maladie de Niemann-Pick type D (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

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

919031000172116 maladie de Niemann-Pick type D fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Niemann-Pick disease, type D	est un(e) (attribut)	Sphingomyelin/cholesterol lipidosis (disorder)	true	Inferred relationship	Some
Niemann-Pick disease, type D	morphologie associée (attribut)	Niemann-Pick cell (cell)	false	Inferred relationship	Some
Niemann-Pick disease, type D	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Niemann-Pick disease, type D	morphologie associée (attribut)	Foam cell (cell)	false	Inferred relationship	Some
Niemann-Pick disease, type D	survenue (attribut)	congénital	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets