ICD-10: A81.83

obsolete genetic disorder fatal familial insomnia electroclinical syndrome variable age at onset electroclinical syndrome X-linked monogenic disease autosomal dominant disease autosomal recessive disease Y-linked monogenic disease autosomal genetic disease obsolete CLN3 disease obsolete paramyloidosis Ogden syndrome familial encephalopathy with neuroserpin inclusion bodies spinocerebellar ataxia type 10 spinocerebellar ataxia type 26 spinocerebellar ataxia type 40 autoimmune disease of central nervous system obsolete neurological disorder GABA aminotransferase deficiency CEDNIK syndrome Stormorken syndrome Kufor-Rakeb syndrome Christianson syndrome