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 39101 - 39125 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0017661 IGA Glomerulonephritis NEU1 4758 neuraminidase 1 Q99519
C0007138 Carcinoma, Transitional Cell NEU1 4758 neuraminidase 1 Q99519
C0162819 Skin Diseases, Vascular NEU1 4758 neuraminidase 1 Q99519
C0271650 Impaired glucose tolerance NEU1 4758 neuraminidase 1 Q99519
C1458155 Mammary Neoplasms NEU1 4758 neuraminidase 1 Q99519
C3714756 Intellectual Disability NEU1 4758 neuraminidase 1 Q99519
C4282398 Sialidase deficiency NEU1 4758 neuraminidase 1 Q99519
C0001418 Adenocarcinoma NEU1 4758 neuraminidase 1 Q99519
C0751776 Atypical Inclusion-Body Disease NEU1 4758 neuraminidase 1 Q99519
C0025362 Mental Retardation NEU1 4758 neuraminidase 1 Q99519
C0007134 Renal Cell Carcinoma NEU1 4758 neuraminidase 1 Q99519
C0004114 Astrocytoma NEU1 4758 neuraminidase 1 Q99519
C0003873 Rheumatoid Arthritis NEU1 4758 neuraminidase 1 Q99519
C0086795 Pfaundler-Hurler Syndrome NEU1 4758 neuraminidase 1 Q99519
C1861305 TARSAL-CARPAL COALITION SYNDROME NEU1 4758 neuraminidase 1 Q99519
C0029463 Osteosarcoma NEU1 4758 neuraminidase 1 Q99519
C0025202 melanoma NEU1 4758 neuraminidase 1 Q99519
C0015393 Eye Abnormalities NEU1 4758 neuraminidase 1 Q99519
C0007131 Non-Small Cell Lung Carcinoma NEU1 4758 neuraminidase 1 Q99519
C0034069 Pulmonary Fibrosis NEU1 4758 neuraminidase 1 Q99519
C0279680 Transitional cell carcinoma of bladder NEU1 4758 neuraminidase 1 Q99519
C0029422 Osteochondrodysplasias NEU1 4758 neuraminidase 1 Q99519
C0009324 Ulcerative Colitis NEU1 4758 neuraminidase 1 Q99519
C0268228 Neuraminidase 1 deficiency NEU1 4758 neuraminidase 1 Q99519
C0042900 Vitiligo NEU1 4758 neuraminidase 1 Q99519

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Last updated: August 19, 2024