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 11901 - 11925 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0376358 Malignant neoplasm of prostate PTGDS 5730 prostaglandin D2 synthase P41222
C0028754 Obesity PTGDS 5730 prostaglandin D2 synthase P41222
C0600139 Prostate carcinoma PTGDS 5730 prostaglandin D2 synthase P41222
C0006271 Bronchiolitis PTGDS 5730 prostaglandin D2 synthase P41222
C0011849 Diabetes Mellitus PTGDS 5730 prostaglandin D2 synthase P41222
C0266929 Chronic Periodontitis PTGDS 5730 prostaglandin D2 synthase P41222
C0014070 Encephalomyelitis PTGDS 5730 prostaglandin D2 synthase P41222
C0038506 Stuttering PTGDS 5730 prostaglandin D2 synthase P41222
C0018776 Hearing Loss, Central PTGDS 5730 prostaglandin D2 synthase P41222
C0021841 Intestinal Neoplasms PTGDS 5730 prostaglandin D2 synthase P41222
C0024117 Chronic Obstructive Airway Disease PTGDS 5730 prostaglandin D2 synthase P41222
C4721610 Carcinoma, Ovarian Epithelial PTGDS 5730 prostaglandin D2 synthase P41222
C0311237 Goniodysgenesis PTGDS 5730 prostaglandin D2 synthase P41222
C0011603 Dermatitis PTGDS 5730 prostaglandin D2 synthase P41222
C0006277 Bronchitis PTGDS 5730 prostaglandin D2 synthase P41222
C0024121 Lung Neoplasms PTGDS 5730 prostaglandin D2 synthase P41222
C0577631 Carotid Atherosclerosis PTGDS 5730 prostaglandin D2 synthase P41222
C0018780 Hearing Loss, High-Frequency PTGDS 5730 prostaglandin D2 synthase P41222
C0004936 Mental disorders PTGDS 5730 prostaglandin D2 synthase P41222
C0040128 Thyroid Diseases PTGDS 5730 prostaglandin D2 synthase P41222
C1140680 Malignant neoplasm of ovary PTEN 5728 phosphatase and tensin homolog P60484
C0149925 Small cell carcinoma of lung PTEN 5728 phosphatase and tensin homolog P60484
C0476089 Endometrial Carcinoma PTEN 5728 phosphatase and tensin homolog P60484
C0018553 Hamartoma Syndrome, Multiple PTEN 5728 phosphatase and tensin homolog P60484
C1332206 Adult Lymphoma PTEN 5728 phosphatase and tensin homolog P60484

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Last updated: August 19, 2024