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\Neurological disorder\Hereditary disorder of nervous system\Amyotrophic lateral sclerosis type 10
• \Disorder of body system\Neurological disorder\Chronic nervous system disorder\Amyotrophic lateral sclerosis type 10
• \Disorder of body system\Neurological disorder\Motor neurone disease\Amyotrophic lateral sclerosis\Amyotrophic lateral sclerosis type 10
• \Chronic disease\Chronic nervous system disorder\Amyotrophic lateral sclerosis type 10

Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4964309016	ALS10 - amyotrophic lateral sclerosis type 10	en	Synonym	Active	Case sensitive	SNOMED CT core
4964310014	Amyotrophic lateral sclerosis type 10 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4964311013	Amyotrophic lateral sclerosis type 10	en	Synonym	Active	Case insensitive	SNOMED CT core
4964314017	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. There is evidence this disease is caused by heterozygous mutation in the TARDBP gene that encodes the TDP43 protein on chromosome 1p36.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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