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 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:G12.2 (Orphanet:803)
  • MedDRA:10002026 (Orphanet:803)
  • SCTID:86044005 (MONDO:equivalentTo)
  • ICD9:335.20 (i2s)
  • DOID:332 (MONDO:equivalentTo)
  • UMLS:C0002736 (Orphanet:803)
  • KEGG:05014 (MONDO:equivalentTo)
  • NIFSTD:birnlex_12566 (EFO:0000253)
  • GARD:0005786 (Orphanet-shared)
  • NCIT:C34373 (exact-label-match)
  • MESH:D000690 (Orphanet:803)
  • COHD:373182 (MONDO:equivalentTo)
  • Orphanet:803 (MONDO:equivalentTo)
  • ICD10:G12.21 (MONDO:equivalentTo)
  • EFO:0000253 (MONDO:equivalentTo)
Subsets

ordo_disease

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

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/meddra/10002026

http://identifiers.org/snomedct/86044005

http://identifiers.org/mesh/D000690

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

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

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

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

has exact synonym

Lou Gehrig disease

Charcot disease

ALS

motor neuron disease, bulbar

Lou Gehrig's disease

id

MONDO:0004976