You are using an outdated browser. Please upgrade your browser to improve your experience.

juvenile amyotrophic lateral sclerosis

Disease Summary
Associated Targets (4)
Tbio

3

Tclin

1


GARD Rare
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0017593:  juvenile amyotrophic lateral sclerosis
GARD:0011901: 
Orphanet:300605: 
SCTID:718555006: 
UMLS:C3468114: 
UMLS:CN239582: