1208412003: Amyotrophic lateral sclerosis type 10 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 10
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Amyotrophic lateral sclerosis type 10
• \Degenerative disorder\Amyotrophic lateral sclerosis type 10
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 10
• \Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 10
• \Disorder of body system\Disorder of nervous system\Chronic nervous system disorder\Amyotrophic lateral sclerosis type 10
• \Disorder of body system\Disorder of nervous system\Motor neuron disease\Amyotrophic lateral sclerosis\Amyotrophic lateral sclerosis type 10
• \Chronic disease\Chronic nervous system disorder\Amyotrophic lateral sclerosis type 10

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4964309016	ALS10 - amyotrophic lateral sclerosis type 10	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4964310014	Amyotrophic lateral sclerosis type 10 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4964311013	Amyotrophic lateral sclerosis type 10	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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