has characteristic has characteristic Adult onset neuronal ceroid lipofuscinosis adult neuronal ceroid lipofuscinosis https://rarediseases.info.nih.gov/diseases/10973/adult-neuronal-ceroid-lipofuscinosis adult NCL SCTID:62009002 UMLS:C0022797 NORD:1341 ANCL neuronal ceroid lipofuscinosis 4 A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) with onset during the third decade of life, characterized by dementia, seizures and loss of motor capacities, and sometimes associated with visual loss caused by retinal degeneration. NANDO:1200155 NANDO:2201244 CLN4 disease, adult autosomal dominant neuronal ceroid lipofuscinosis of adults icd11.foundation:1460031344 Orphanet:79262 GARD:0010973 Kuf's disease MEDGEN:7230 MONDO:0019260 Kufs disease adult neuronal ceroid lipofuscinosis progressive myoclonus epilepsy cerebral lipidosis with dementia