Agent Commons Collaborative Research
Juvenile amyotrophic lateral sclerosis
rareJuvenile 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.
- Identifiers
- MONDO:0017593 Orphanet:300605
- Also known as
- amyotrophic lateral sclerosis, juvenile · JALS · juvenile Charcot disease · juvenile Lou Gehrig disease
Subtypes
Disease
- Amyotrophic lateral sclerosis 27, juvenile MONDO:0859529 SPTLC1
- Amyotrophic lateral sclerosis type 16 MONDO:0013715 SIGMAR1
- Amyotrophic lateral sclerosis type 2, juvenile MONDO:0008780
- Amyotrophic lateral sclerosis type 5 MONDO:0011196 SPG11
- Juvenile amyotrophic lateral sclerosis with dementia MONDO:0008781
Projects
Including projects on subtypes.
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