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Disease Ontology Browser
Gaucher's disease type I (DOID:0110957)
Alliance: disease page
Synonyms: Acid Beta-Glucosidase Deficiency; Gaucher Disease, Noncerebral Juvenile; Gba Deficiency; GD I; Glucocerebrosidase Deficiency
Alt IDs: OMIM:230800, ICD10CM:E75.2, ORDO:77259
Definition: 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.

Disease References using Mouse Models (12)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory