neuronal ceroid lipofuscinosis 3 ORDO:228346 ICD10CM:E75.4 A neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive dementia, seizures, and progressive visual failure and an ultrastructural pattern of lipopigment with a 'fingerprint' profile and has_material_basis_in homozygous or compound heterozygous mutation in the CLN3 gene on chromosome 16p11. Batten disease GARD:5897 OMIM:204200 disease_ontology CLN3 DOID:0110731 DOID:0050756 juvenile neuronal ceroid lipofuscinosis neuronal ceroid lipofuscinosis genetic disease