784341001: Amyotrophic lateral sclerosis type 4 (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Amyotrophic lateral sclerosis type 4
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Amyotrophic lateral sclerosis type 4
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Amyotrophic lateral sclerosis type 4
• \Disease\affection dégénérative\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Amyotrophic lateral sclerosis type 4
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Amyotrophic lateral sclerosis type 4
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Amyotrophic lateral sclerosis type 4
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\trouble neurologique chronique\Amyotrophic lateral sclerosis type 4
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\maladie du motoneurone (trouble)\Amyotrophic lateral sclerosis\Amyotrophic lateral sclerosis type 4
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Amyotrophic lateral sclerosis type 4
• \Disease\maladie chronique\trouble neurologique chronique\Amyotrophic lateral sclerosis type 4

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3763685016	Amyotrophic lateral sclerosis type 4	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763686015	ALS4 - amyotrophic lateral sclerosis type 4	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3763687012	dHMN (distal hereditary motor neuropathy) with upper motor neuron signs	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3763688019	Amyotrophic lateral sclerosis type 4 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763689010	A rare genetic motor neuron disease with characteristics of late childhood or adolescent onset of slowly progressive severe distal limb muscle weakness and wasting, in association with pyramidal signs, normal sensation and absence of bulbar involvement. Leads to degeneration of motor neurons in the brain and spinal cord.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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