DO_rare_slim has material basis in has symptom disease has feature autosomal dominant disease cerebellar ataxia subjective cognitive decline neuronal ceroid lipofuscinosis 4 ORDO:228343 A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inheritance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene on chromosome 20q13. ICD10CM:E75.4 disease_ontology MIM:162350 CLN4B disease DOID:0110720 autosomal dominant neuronal ceroid lipofuscinosis 4B neuronal ceroid lipofuscinosis 4 Parry type neuronal ceroid lipofuscinosis 4B neuronal ceroid lipofuscinosis autosomal dominant inheritance seizure