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amyotrophic lateral sclerosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0004976

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. [ Orphanet:803 ]

Synonyms: Lou Gehrig disease Charcot disease ALS Lou Gehrig's disease motor neuron disease, bulbar amyotrophic lateral sclerosis

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:332 (MONDO:equivalentTo)
  • Orphanet:803 (MONDO:equivalentTo)
  • GARD:5786 (MONDO:GARD)
  • SCTID:86044005 (MONDO:equivalentTo)
  • NIFSTD:birnlex_12566 (EFO:0000253)
  • UMLS:C0002736 (MONDO:equivalentTo)
  • MEDGEN:274 (MONDO:equivalentTo)
  • NCIT:C34373 (MONDO:exact-label-match)
  • MedDRA:10002026 (Orphanet:803/e)
  • MESH:D000690 (Orphanet:803/e)
  • ICD9:335.20 (MONDO:i2s)
  • ICD10CM:G12.21 (MONDO:equivalentTo)
  • NORD:768 (MONDO:NORD)
  • icd11.foundation:1982355687 (Orphanet:803)
  • NANDO:1200002 (https://orcid.org/0000-0003-0011-764X)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare, clingen

closeMatch

http://identifiers.org/meddra/10002026

exactMatch

http://identifiers.org/snomedct/86044005

http://identifiers.org/mesh/D000690

http://linkedlifedata.com/resource/umls/id/C0002736

http://purl.bioontology.org/ontology/ICD10CM/G12.21

http://www.orpha.net/ORDO/Orphanet_803

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

http://identifiers.org/medgen/274

http://purl.obolibrary.org/obo/NCIT_C34373

id

MONDO:0004976

Term relations