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 6976 - 7000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
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
C3888317 Sialidosis, type 2 NEU1 4758 neuraminidase 1 Q99519
C0033687 Proteinuria NEU1 4758 neuraminidase 1 Q99519
C1332166 Adenocarcinoma of the gastroesophageal junction NEU1 4758 neuraminidase 1 Q99519
C0035309 Retinal Diseases NEU1 4758 neuraminidase 1 Q99519
C0018784 Sensorineural Hearing Loss (disorder) NEU1 4758 neuraminidase 1 Q99519
C0206701 Cystadenocarcinoma, Serous NEU1 4758 neuraminidase 1 Q99519
C2607914 Allergic rhinitis (disorder) NEU1 4758 neuraminidase 1 Q99519
C0007138 Carcinoma, Transitional Cell NEU1 4758 neuraminidase 1 Q99519
C2239176 Liver carcinoma NEU1 4758 neuraminidase 1 Q99519
C2718068 beta-Galactosidase Deficiency NEU1 4758 neuraminidase 1 Q99519
C0028738 Nystagmus NEU1 4758 neuraminidase 1 Q99519
C0009324 Ulcerative Colitis NEU1 4758 neuraminidase 1 Q99519

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Last updated: August 19, 2024