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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. [ url:http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis url:http://www.ninds.nih.gov/disorders/amyotrophiclateralsclerosis/detail_ALS.htm ]

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

Term info

database cross reference
  • ICD10CM:G12.21
  • OMIM:PS105400
  • SNOMEDCT_US_2016_03_01:86044005
  • UMLS_CUI:C0002736
  • NCI:C34373
  • ORDO:803
  • ICD9CM:335.20
  • MESH:D000690
  • KEGG:05014
  • EFO:0000253
Subsets

DO_FlyBase_slim

has obo namespace

disease_ontology

id

DOID:332

Term relations

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