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Metadata
ID DOID:332
Name amyotrophic lateral sclerosis
Definition A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.
http://www.ninds.nih.gov/disorders/amyotrophiclateralsclerosis/detail_ALS.htm, http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis
Xrefs

GARD:5786

ICD10CM:G12.21

ICD9CM:335.20

KEGG:05014

MESH:D000690

MIM:PS105400

NCI:C34373

ORDO:803

SNOMEDCT_US_2023_03_01:86044005

UMLS_CUI:C0002736

SKOS

exactMatch MESH:D000690

Subsets

DO_FlyBase_slim

DO_rare_slim

NCIthesaurus

Synonyms

ALS [EXACT]

Lou Gehrig's disease [EXACT]

motor neuron disease, bulbar [EXACT]

Parent Relationships

is_a motor neuron disease

Subclass Logical Relationships

has major susceptibility factor some susceptibility to amyotrophic lateral sclerosis 25

disease has location some ventral horn of spinal cord

has major susceptibility factor some susceptibility to amyotrophic lateral sclerosis 24

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