Agent Commons Collaborative Research

ALS2-related motor neuron disease

rare

Any motor neuron disease in which the cause of the disease is a mutation in the ALS2 gene.

Identifiers
MONDO:0100227
Causal genes
ALS2
Part of
Hereditary motor neuron disease
Also known as
Alsin-related motor neuron disease

Subtypes

All diseases Rare only
Disease Subtypes
Amyotrophic lateral sclerosis type 2, juvenile
Infantile-onset ascending hereditary spastic paralysis
Juvenile primary lateral sclerosis

Rare disease

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