amyotrophic lateral sclerosis

amyotrophic lateral sclerosis

http://purl.obolibrary.org/obo/DOID_332

A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing. [ http://purl.obolibrary.org/obo/ECO_0007638 url:http://www.ninds.nih.gov/disorders/amyotrophiclateralsclerosis/detail_ALS.htm url:http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis ]

Synonyms: ALS motor neuron disease, bulbar Lou Gehrig's disease

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This is just here as a test because I lose it

Term information

database cross reference

ICD9CM:335.20
GARD:5786
MESH:D000690
MIM:PS105400
KEGG:05014
ICD10CM:G12.21
NCI:C34373
ORDO:803
SNOMEDCT_US_2023_03_01:86044005
UMLS_CUI:C0002736

Subsets

DO_FlyBase_slim, DO_rare_slim, NCIthesaurus

acronym

ALS

has exact match

MESH:D000690

has obo namespace

disease_ontology

DOID:332

Term relations

Subclass of:

motor neuron disease
disease has location some ventral horn of spinal cord

Related from:

contributes to condition

susceptibility to amyotrophic lateral sclerosis 24
susceptibility to amyotrophic lateral sclerosis 25