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 51 - 75 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0005695 Bladder Neoplasm XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0006826 Malignant Neoplasms XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0011570 Mental Depression XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0019348 Herpes Simplex Infections XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0005684 Malignant neoplasm of urinary bladder XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0021775 Intermittent Claudication XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0242383 Age related macular degeneration XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0473583 Nevus elasticus XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0553580 Ewings sarcoma XYLT2 64132 xylosyltransferase 2 Q9H1B5
C3714756 Intellectual Disability XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0011581 Depressive disorder XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0023480 Leukemia, Myelomonocytic, Chronic XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0008354 Cholera XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0018784 Sensorineural Hearing Loss (disorder) XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0085580 Essential Hypertension XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0376359 Gronblad-Strandberg Syndrome XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0022658 Kidney Diseases XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0018818 Ventricular Septal Defects XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0085669 Acute leukemia XYLT2 64132 xylosyltransferase 2 Q9H1B5
C1561643 Chronic Kidney Diseases XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0042769 Virus Diseases XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0026267 Mitral Valve Prolapse Syndrome XYLT2 64132 xylosyltransferase 2 Q9H1B5
C1535939 Pneumocystis jiroveci pneumonia XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0002418 Amblyopia XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0030567 Parkinson Disease XYLT2 64132 xylosyltransferase 2 Q9H1B5

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Last updated: August 19, 2024