1201950008: Amyotrophic lateral sclerosis type 3 (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\...
• \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
• \affection dégénérative\Amyotrophic lateral sclerosis type 3
• \affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 3
• \affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 3
• \affection d'un système corporel\Disorder of nervous system (disorder)\trouble neurologique chronique\Amyotrophic lateral sclerosis type 3
• \affection d'un système corporel\Disorder of nervous system (disorder)\maladie du motoneurone (trouble)\Amyotrophic lateral sclerosis\Amyotrophic lateral sclerosis type 3
• \maladie chronique\trouble neurologique chronique\Amyotrophic lateral sclerosis type 3

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4945860011	Amyotrophic lateral sclerosis type 3	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4945861010	Amyotrophic lateral sclerosis type 3 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4945862015	ALS3 - amyotrophic lateral sclerosis type 3	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4945863013	A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Associated with the ALS3 gene on the cytogenetic location 18q21.	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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