DisGeNET

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.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 13676 - 13700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0009404 Colorectal Neoplasms PLD2 5338 phospholipase D2 O14939
C0018802 Congestive heart failure PLD2 5338 phospholipase D2 O14939
C0524620 Metabolic Syndrome X PLD2 5338 phospholipase D2 O14939
C0006079 Bowen's Disease PLD2 5338 phospholipase D2 O14939
C0023448 Lymphoid leukemia PLD2 5338 phospholipase D2 O14939
C0032285 Pneumonia PLD2 5338 phospholipase D2 O14939
C1561643 Chronic Kidney Diseases PLD2 5338 phospholipase D2 O14939
C0022602 Actinic keratosis PLD2 5338 phospholipase D2 O14939
C0278878 Adult Glioblastoma PLD2 5338 phospholipase D2 O14939
C0036572 Seizures PLD2 5338 phospholipase D2 O14939
C1621958 Glioblastoma Multiforme PLD2 5338 phospholipase D2 O14939
C0018801 Heart failure PLD2 5338 phospholipase D2 O14939
C0002395 Alzheimer's Disease PLD2 5338 phospholipase D2 O14939
C0270824 Visual seizure PLD2 5338 phospholipase D2 O14939
C0162429 Malnutrition PLD2 5338 phospholipase D2 O14939
C0007137 Squamous cell carcinoma PLD2 5338 phospholipase D2 O14939
C0009375 Colonic Neoplasms PLD2 5338 phospholipase D2 O14939
C0017638 Glioma PLD2 5338 phospholipase D2 O14939
C0017636 Glioblastoma PLD2 5338 phospholipase D2 O14939
C0035309 Retinal Diseases PLD2 5338 phospholipase D2 O14939
C0751955 Brain Infarction PLD2 5338 phospholipase D2 O14939
C0014556 Epilepsy, Temporal Lobe PLD2 5338 phospholipase D2 O14939
C0020608 Hypodontia PLD2 5338 phospholipase D2 O14939
C0020538 Hypertensive disease PLD2 5338 phospholipase D2 O14939
C0376358 Malignant neoplasm of prostate PLD2 5338 phospholipase D2 O14939

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Last updated: August 19, 2024