Any motor neuron disease in which the cause of the disease is a mutation in the ALS2 gene.
Comprehensive, easy-to-understand information about this condition
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prenatal-onset spinal muscular atrophy with congenital bone fractures
MONDO:0000209
spinal muscular atrophy
MONDO:0001516
familial amyotrophic lateral sclerosis
MONDO:0005144
neurogenic scapuloperoneal syndrome, Kaeser type
MONDO:0008407
amyotrophic lateral sclerosis type 2, juvenile
MONDO:0008780
riboflavin transporter deficiency
MONDO:0008891