Amyotrophic lateral sclerosis

rare

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.

Identifiers: MONDO:0004976 Orphanet:803
Part of: Anterior horn disorder Motor neuron disorder
Also known as: ALS · Charcot disease · Lou Gehrig disease

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Familial amyotrophic lateral sclerosis	MONDO:0005144	33
Progressive muscular atrophy	MONDO:0018687	1
Amyotrophic lateral sclerosis with polyglucosan bodies	MONDO:0008782
Sporadic amyotrophic lateral sclerosis	MONDO:0005145

Rare disease

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