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 61701 - 61725 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0085110 Severe Combined Immunodeficiency HPSE 10855 heparanase Q9Y251
C0019156 Hepatic Veno-Occlusive Disease HPSE 10855 heparanase Q9Y251
C0023448 Lymphoid leukemia HPSE 10855 heparanase Q9Y251
C0029463 Osteosarcoma HPSE 10855 heparanase Q9Y251
C0017661 IGA Glomerulonephritis HPSE 10855 heparanase Q9Y251
C0279607 Adult Hepatocellular Carcinoma HPSE 10855 heparanase Q9Y251
C0027086 Myoma HPSE 10855 heparanase Q9Y251
C0585442 Osteosarcoma of bone HPSE 10855 heparanase Q9Y251
C0033860 Psoriasis HPSE 10855 heparanase Q9Y251
C0153349 Malignant neoplasm of tongue HPSE 10855 heparanase Q9Y251
C0272286 Thrombocytopenia due to platelet alloimmunization HPSE 10855 heparanase Q9Y251
C2717836 Steroid Sulfatase Deficiency Disease HPSE 10855 heparanase Q9Y251
C0008497 Choriocarcinoma HPSE 10855 heparanase Q9Y251
C0018799 Heart Diseases HPSE 10855 heparanase Q9Y251
C0685938 Malignant neoplasm of gastrointestinal tract HPSE 10855 heparanase Q9Y251
C0154841 Central retinal vein occlusion HPSE 10855 heparanase Q9Y251
C0878544 Cardiomyopathies HPSE 10855 heparanase Q9Y251
C0003467 Anxiety HPSE 10855 heparanase Q9Y251
C0020456 Hyperglycemia HPSE 10855 heparanase Q9Y251
C0017668 Focal glomerulosclerosis HPSE 10855 heparanase Q9Y251
C1442903 Exostoses HPSE 10855 heparanase Q9Y251
C0009404 Colorectal Neoplasms HPSE 10855 heparanase Q9Y251
C0403396 Steroid-sensitive nephrotic syndrome HPSE 10855 heparanase Q9Y251
C0154830 Proliferative diabetic retinopathy HPSE 10855 heparanase Q9Y251
C0279070 Adult Oligodendroglioma HPSE 10855 heparanase Q9Y251

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Last updated: August 19, 2024