has material basis in germline mutation in ATP13A2 juvenile-onset Parkinson disease Kufor-Rakeb syndrome https://www.malacards.org/card/kufor_rakeb_syndrome OMIM:606693 PARK9 UMLS:C1847640 ceroid lipofuscinosis, neuronal, 12 Kufor Rakeb Syndrome MONDO:0011706 park 9 Parkinson disease 9, autosomal recessive KRPPD Orphanet:306674 Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia Parkinson disease type 9 NORD:1959 Parkinson disease 9, autosomal recessive, juvenile-onset MEDGEN:338281 Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment. GARD:0009174 KRS DOID:0060556 MESH:C537177 Kufor-Rakeb syndrome Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia neurodegeneration with brain iron accumulation