64383006: Werdnig-Hoffmann disease (disorder)

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

\Genetic disease\maladie héréditaire\...

\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease (disorder)\atrophie musculaire spinale (trouble)\Werdnig-Hoffmann disease

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Werdnig-Hoffmann disease

\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease (disorder)\atrophie musculaire spinale (trouble)\Werdnig-Hoffmann disease
\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary motor neuron disease (disorder)\atrophie musculaire spinale (trouble)\Werdnig-Hoffmann disease
\affection d'un système corporel\Disorder of nervous system (disorder)\maladie du motoneurone (trouble)\Lower motor neuron disease\Anterior horn cell disease\Werdnig-Hoffmann disease
\affection d'un système corporel\Disorder of nervous system (disorder)\maladie du motoneurone (trouble)\Lower motor neuron disease\atrophie musculaire spinale (trouble)\Werdnig-Hoffmann disease
\affection d'un système corporel\Disorder of nervous system (disorder)\maladie du motoneurone (trouble)\Hereditary motor neuron disease (disorder)\atrophie musculaire spinale (trouble)\Werdnig-Hoffmann disease

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

107017013 Werdnig-Hoffmann disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

107018015 Infantile spinal muscular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

107019011 Progressive muscular atrophy of infancy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1232557016 Spinal muscular atrophy type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1232558014 WHD - Werdnig-Hoffmann disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

199235017 Spinal muscular atrophy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

452331000241111 maladie de Werdnig-Hoffmann (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

467091000172113 maladie de Werdnig-Hoffmann fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

803770017 Werdnig-Hoffmann disease (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
Werdnig-Hoffmann disease	est un(e) (attribut)	Anterior horn cell disease	true	Inferred relationship	Some
Werdnig-Hoffmann disease	localisation d'une constatation (attribut)	système nerveux	true	Inferred relationship	Some	1
Werdnig-Hoffmann disease	est un(e) (attribut)	atrophie musculaire spinale (trouble)	true	Inferred relationship	Some
Werdnig-Hoffmann disease	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Werdnig-Hoffmann disease	morphologie associée (attribut)	dégénérescence	false	Inferred relationship	Some	2
Werdnig-Hoffmann disease	localisation d'une constatation (attribut)	Motor neuron	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)