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 41551 - 41575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0400966 Non-alcoholic Fatty Liver Disease NEU1 4758 neuraminidase 1 Q99519
C0019294 Hernia, Inguinal NEU1 4758 neuraminidase 1 Q99519
C0027766 Nervous System Neoplasms NEU1 4758 neuraminidase 1 Q99519
C0585474 Ewing's sarcoma of bone NEU1 4758 neuraminidase 1 Q99519
C0029422 Osteochondrodysplasias NEU1 4758 neuraminidase 1 Q99519
C0007124 Noninfiltrating Intraductal Carcinoma NEU1 4758 neuraminidase 1 Q99519
C1368019 Paget Disease NEU1 4758 neuraminidase 1 Q99519
C0004153 Atherosclerosis NEU1 4758 neuraminidase 1 Q99519
C0878544 Cardiomyopathies NEU1 4758 neuraminidase 1 Q99519
C0000768 Congenital Abnormality NEU1 4758 neuraminidase 1 Q99519
C0021400 Influenza NEU1 4758 neuraminidase 1 Q99519
C0854924 Papillary serous endometrial carcinoma NEU1 4758 neuraminidase 1 Q99519
C0376358 Malignant neoplasm of prostate NEU1 4758 neuraminidase 1 Q99519
C1332986 Childhood Osteosarcoma NEU1 4758 neuraminidase 1 Q99519
C0751779 Action Myoclonus-Renal Failure Syndrome NEU1 4758 neuraminidase 1 Q99519
C0003873 Rheumatoid Arthritis NEU1 4758 neuraminidase 1 Q99519
C0162819 Skin Diseases, Vascular NEU1 4758 neuraminidase 1 Q99519
C0279680 Transitional cell carcinoma of bladder NEU1 4758 neuraminidase 1 Q99519
C0027697 Nephritis NEU1 4758 neuraminidase 1 Q99519
C0751781 Dentatorubral-Pallidoluysian Atrophy NEU1 4758 neuraminidase 1 Q99519
C0036439 Scoliosis, unspecified NEU1 4758 neuraminidase 1 Q99519
C0086543 Cataract NEU1 4758 neuraminidase 1 Q99519
C1621958 Glioblastoma Multiforme NEU1 4758 neuraminidase 1 Q99519
C0015393 Eye Abnormalities NEU1 4758 neuraminidase 1 Q99519
C0042900 Vitiligo NEU1 4758 neuraminidase 1 Q99519

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Last updated: August 19, 2024