gaucher disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver. (Human Disease Ontology, DOID_1926)
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4 genes associated with the disease gaucher disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
GBA glucosidase, beta, acid
IL6 interleukin 6
NTRK3 neurotrophic tyrosine kinase, receptor, type 3