Search
Specific
congenital hypomyelination neuropathy
familial amyloid polyneuropathy
Finnish type amyloidosis; amyloidosis type 5; Meretoja type amyloidosis
giant axonal neuropathy
hereditary neuropathy
oculoleptomeningeal type amyloidosis (amyloidosis VII)
spastic ataxia of Charlevoix-Saguenay
General
genetic disease of the nervous system