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 1076 - 1100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0004153 Atherosclerosis HPSE 10855 heparanase Q9Y251
C0035309 Retinal Diseases HPSE 10855 heparanase Q9Y251
C3463824 MYELODYSPLASTIC SYNDROME HPSE 10855 heparanase Q9Y251
C0003873 Rheumatoid Arthritis HPSE 10855 heparanase Q9Y251
C1257931 Mammary Neoplasms, Human HPSE 10855 heparanase Q9Y251
C0278510 Childhood Medulloblastoma HPSE 10855 heparanase Q9Y251
C4721453 Peripheral Nervous System Diseases HPSE 10855 heparanase Q9Y251
C0017601 Glaucoma HPSE 10855 heparanase Q9Y251
C0155626 Acute myocardial infarction HPSE 10855 heparanase Q9Y251
C0023449 Acute lymphocytic leukemia HPSE 10855 heparanase Q9Y251
C0017636 Glioblastoma HPSE 10855 heparanase Q9Y251
C0684249 Carcinoma of lung HPSE 10855 heparanase Q9Y251
C0948008 Ischemic stroke HPSE 10855 heparanase Q9Y251
C0017658 Glomerulonephritis HPSE 10855 heparanase Q9Y251
C0001339 Acute pancreatitis HPSE 10855 heparanase Q9Y251
C0003850 Arteriosclerosis HPSE 10855 heparanase Q9Y251
C0152018 Esophageal carcinoma HPSE 10855 heparanase Q9Y251
C0019196 Hepatitis C HPSE 10855 heparanase Q9Y251
C1334177 Infiltrating Cervical Carcinoma HPSE 10855 heparanase Q9Y251
C0546837 Malignant neoplasm of esophagus HPSE 10855 heparanase Q9Y251
C0040034 Thrombocytopenia HPSE 10855 heparanase Q9Y251
C0017638 Glioma HPSE 10855 heparanase Q9Y251
C0035412 Rhabdomyosarcoma HPSE 10855 heparanase Q9Y251
C0278996 Malignant Head and Neck Neoplasm HPSE 10855 heparanase Q9Y251
C0007820 Cerebrovascular Disorders HPSE 10855 heparanase Q9Y251

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Last updated: August 19, 2024