Term Name:	neuronal ceroid lipofuscinosis 13
Synonyms:	CLN13, neuronal ceroid lipofuscinosis 13 Kufs type
Definition:	A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with adult onset of progressive cognitive decline and motor dysfunction leading to dementia and often early death and has_material_basis_in homozygous or compound heterozygous mutation in the CTSF gene on chromosome 11q13.
Ontology:	Human Disease [DOID:0110727]   ( DOID:0110727 )