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 61676 - 61700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0333875 High-Grade Squamous Intraepithelial Lesions HPSE 10855 heparanase Q9Y251
C0007103 Malignant neoplasm of endometrium HPSE 10855 heparanase Q9Y251
C1848296 DOSAGE-SENSITIVE SEX REVERSAL HPSE 10855 heparanase Q9Y251
C0026769 Multiple Sclerosis HPSE 10855 heparanase Q9Y251
C0011603 Dermatitis HPSE 10855 heparanase Q9Y251
C1261473 Sarcoma HPSE 10855 heparanase Q9Y251
C0002448 Ameloblastoma HPSE 10855 heparanase Q9Y251
C0278878 Adult Glioblastoma HPSE 10855 heparanase Q9Y251
C1168401 Squamous cell carcinoma of the head and neck HPSE 10855 heparanase Q9Y251
C0019829 Hodgkin Disease HPSE 10855 heparanase Q9Y251
C0011875 Diabetic Angiopathies HPSE 10855 heparanase Q9Y251
C0162569 Hepatoerythropoietic Porphyria HPSE 10855 heparanase Q9Y251
C0281361 Adenocarcinoma of pancreas HPSE 10855 heparanase Q9Y251
C0015306 Hereditary Multiple Exostoses HPSE 10855 heparanase Q9Y251
C0039101 synovial sarcoma HPSE 10855 heparanase Q9Y251
C0024530 Malaria HPSE 10855 heparanase Q9Y251
C0280324 Laryngeal Squamous Cell Carcinoma HPSE 10855 heparanase Q9Y251
C0086445 Idiopathic Membranous Glomerulonephritis HPSE 10855 heparanase Q9Y251
C0035344 Retinopathy of Prematurity HPSE 10855 heparanase Q9Y251
C0021051 Immunologic Deficiency Syndromes HPSE 10855 heparanase Q9Y251
C0400966 Non-alcoholic Fatty Liver Disease HPSE 10855 heparanase Q9Y251
C0007131 Non-Small Cell Lung Carcinoma HPSE 10855 heparanase Q9Y251
C0019163 Hepatitis B HPSE 10855 heparanase Q9Y251
C0034494 Rabies (disorder) HPSE 10855 heparanase Q9Y251
C0005695 Bladder Neoplasm HPSE 10855 heparanase Q9Y251

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Last updated: August 19, 2024