DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Database | Last Updated |
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DisGeNET | February 14, 2024 |
Disease ID ▲ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
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ANOPHTHALMIA AND PULMONARY HYPOPLASIA
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L1 cell adhesion molecule
|
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ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
pyruvate kinase M1/2
|
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Hypotonia-Cystinuria Syndrome
|
solute carrier family 3 member 1
|
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Dopa-Responsive Dystonia
|
GTP cyclohydrolase 1
|
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Childhood Ataxia with Central Nervous System Hypomyelinization
|
eukaryotic translation initiation factor 2 subunit gamma
|
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Venous Thromboembolism
|
actin beta
|
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TARSAL-CARPAL COALITION SYNDROME
|
ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
|
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TARSAL-CARPAL COALITION SYNDROME
|
cadherin 13
|
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Coronary Artery Disease
|
polypeptide N-acetylgalactosaminyltransferase 2
|
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Coronary Artery Disease
|
phospholipase A2 group VII
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