hyperuricemia Gene Set
| Dataset |
GAD Gene-Disease Associations
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| Category |
disease or phenotype associations
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| Type |
disease |
| Description |
An acquired metabolic disease that has_material_basis_in an abnormally high level of uric acid in the blood. (Human Disease Ontology, DOID_1920)
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| Similar Terms |
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| Downloads & Tools |
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Genes
8 genes associated with the disease hyperuricemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol |
Name |
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ADRB3
|
adrenoceptor beta 3
|
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APOA1
|
apolipoprotein A-I
|
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APOA4
|
apolipoprotein A-IV
|
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APOC3
|
apolipoprotein C-III
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GNB3
|
guanine nucleotide binding protein (G protein), beta polypeptide 3
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MTHFR
|
methylenetetrahydrofolate reductase (NAD(P)H)
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SLC22A12
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solute carrier family 22 (organic anion/urate transporter), member 12
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SLC2A9
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solute carrier family 2 (facilitated glucose transporter), member 9
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