Human genes for Gaucher's disease type I
Gaucher's disease type I [DOID:0110957]
A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22.
Synonyms: Gaucher's disease type I, DOID:0110957, Gauchers disease type I, Acid Beta-Glucosidase Deficiency, Gaucher Disease, Noncerebral Juvenile ...