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 58126 - 58150 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0040517 Gilles de la Tourette syndrome HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0001857 AIDS related complex HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0023470 Myeloid Leukemia HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0011603 Dermatitis HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0003969 Ascorbic Acid Deficiency HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0007124 Noninfiltrating Intraductal Carcinoma HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0021841 Intestinal Neoplasms HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0026848 Myopathy HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0032002 Pituitary Diseases HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C3469521 FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0024121 Lung Neoplasms HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C1855739 Indifference to Pain, Congenital, Autosomal Recessive HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0015230 Exanthema HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0041696 Unipolar Depression HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C1704321 Nephrotic Syndrome, Minimal Change HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0024530 Malaria HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0040136 Thyroid Neoplasm HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0010072 Coronary Thrombosis PLA2G6 8398 phospholipase A2 group VI O60733
C0376358 Malignant neoplasm of prostate PLA2G6 8398 phospholipase A2 group VI O60733
C0242422 Parkinsonian Disorders PLA2G6 8398 phospholipase A2 group VI O60733
C0010068 Coronary heart disease PLA2G6 8398 phospholipase A2 group VI O60733
C0014038 Encephalitis PLA2G6 8398 phospholipase A2 group VI O60733
C0006826 Malignant Neoplasms PLA2G6 8398 phospholipase A2 group VI O60733
C0476089 Endometrial Carcinoma PLA2G6 8398 phospholipase A2 group VI O60733
C0027051 Myocardial Infarction PLA2G6 8398 phospholipase A2 group VI O60733

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Last updated: August 19, 2024