Term Name:	Gaucher's disease type II
Synonyms:	Gaucher Disease, Acute Neuronopathic Type, GD II, GD2, Infantile Cerebral Gaucher Disease
Definition:	A Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22.
Ontology:	Human Disease [DOID:0110958]   ( DOID:0110958 )