Gaucher's disease type III

Summary

DOID:0110959 - Gaucher's disease type III

Disease Ontology 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.

Synonyms: Gaucher Disease, Juvenile And Adult, Cerebral, Gaucher Disease, Subacute Neuronopathic Type, GD III, Gaucher Disease, Chronic Neuronopathic Type

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:231000 - gaucher disease, type iii

MIM:231000 - gaucher disease, type iii

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), Gaucher's disease (is_a)