An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome.
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
sporadic amyotrophic lateral sclerosis
MONDO:0005145
amyotrophic lateral sclerosis type 1
MONDO:0007103
frontotemporal dementia and/or amyotrophic lateral sclerosis 1
MONDO:0007105
neurogenic scapuloperoneal syndrome, Kaeser type
MONDO:0008407