1201950008: Amyotrophic lateral sclerosis type 3 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 3
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Amyotrophic lateral sclerosis type 3
• \Degenerative disorder\Amyotrophic lateral sclerosis type 3
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 3
• \Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 3
• \Disorder of body system\Disorder of nervous system\Chronic nervous system disorder\Amyotrophic lateral sclerosis type 3
• \Disorder of body system\Disorder of nervous system\Motor neuron disease\Amyotrophic lateral sclerosis\Amyotrophic lateral sclerosis type 3
• \Chronic disease\Chronic nervous system disorder\Amyotrophic lateral sclerosis type 3

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4945860011	Amyotrophic lateral sclerosis type 3	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4945861010	Amyotrophic lateral sclerosis type 3 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4945862015	ALS3 - amyotrophic lateral sclerosis type 3	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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