An instance of motor neuron disease that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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Huntington disease and related disorders
MONDO:0000167
prenatal-onset spinal muscular atrophy with congenital bone fractures
MONDO:0000209
agenesis of the corpus callosum with peripheral neuropathy
MONDO:0000902
spinal muscular atrophy
MONDO:0001516
striatonigral degeneration
MONDO:0003122
angioid streaks of choroid
MONDO:0004882