JSON

amyotrophic lateral sclerosis

^ 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 ]

Term info

database cross reference
  • MedDRA:10002026 (Orphanet:803/e)
  • EFO:0000253 (MONDO:equivalentTo)
  • NCIT:C34373 (MONDO:exact-label-match)
  • SCTID:86044005 (MONDO:equivalentTo)
  • UMLS:C0002736 (Orphanet:803/e)
  • NIFSTD:birnlex_12566 (EFO:0000253)
  • Orphanet:803 (MONDO:equivalentTo)
  • GARD:0005786 (MONDO:equivalentTo)
  • DOID:332 (MONDO:equivalentTo)
  • ICD10CM:G12.21 (MONDO:equivalentTo)
  • MESH:D000690 (Orphanet:803/e)
  • ICD9:335.20 (MONDO:i2s)
Subsets

ordo_disease

abbreviation
ALS [ Orphanet:803 DOID:332 NCIT:C34373 ]

closeMatch

http://identifiers.org/meddra/10002026

definition

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.

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://purl.obolibrary.org/obo/DOID_332, http://purl.obolibrary.org/obo/NCIT_C34373, http://purl.obolibrary.org/obo/Orphanet_803

has exact synonym

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

id

MONDO:0004976