Term Name:	Gaucher's disease type III
Synonyms:	Gaucher Disease, Chronic Neuronopathic Type, Gaucher Disease, Juvenile And Adult, Cerebral, Gaucher Disease, Subacute Neuronopathic Type, GD III
Definition:	A Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22.
Ontology:	Human Disease [DOID:0110959]   ( DOID:0110959 )