Juvenile amyotrophic lateral sclerosis

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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.

Synonyms: Juvenile Charcot disease JALS Juvenile Lou Gehrig disease

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:614373 (BTNT (broader term maps to a narrower term))
  • OMIM:205100 (BTNT (broader term maps to a narrower term))
  • ICD-10 (NTBT (narrower term maps to a broader term))
  • ICD-10 (Attributed)
  • OMIM:602099 (BTNT (broader term maps to a narrower term))
hasDbXref

OMIM:602099, OMIM:205100, OMIM:614373, ICD-10:G12.2

notation

ORPHA:300605