JSON

juvenile amyotrophic lateral sclerosis

^ http://purl.obolibrary.org/obo/MONDO_0017593

Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterized by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age. [ Orphanet:300605 ]

Term info

database cross reference
  • UMLS:CN239582 (MONDO:equivalentTo)
  • UMLS:C3468114 (MONDO:equivalentTo)
  • Orphanet:300605 (MONDO:equivalentTo)
  • GARD:0011901 (MONDO:equivalentTo)
  • SCTID:718555006 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

abbreviation
JALS [ Orphanet:300605 ]

definition

Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterized by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN239582, http://purl.obolibrary.org/obo/Orphanet_300605, http://identifiers.org/snomedct/718555006, http://linkedlifedata.com/resource/umls/id/C3468114

has exact synonym

juvenile Charcot disease, JALS, juvenile Lou Gehrig disease

has related synonym

amyotrophic lateral sclerosis, juvenile

id

MONDO:0017593

seeAlso

https://rarediseases.info.nih.gov/diseases/11901/juvenile-amyotrophic-lateral-sclerosis

Term relations