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 14726 - 14750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0340427 Familial dilated cardiomyopathy DOLK 22845 dolichol kinase Q9UPQ8
C0018784 Sensorineural Hearing Loss (disorder) DOLK 22845 dolichol kinase Q9UPQ8
C1449563 Cardiomyopathy, Familial Idiopathic DOLK 22845 dolichol kinase Q9UPQ8
C0699790 Colon Carcinoma NTNG1 22854 netrin G1 Q9Y2I2
C0948008 Ischemic stroke NTNG1 22854 netrin G1 Q9Y2I2
C0206754 Neuroendocrine Tumors NTNG1 22854 netrin G1 Q9Y2I2
C0007102 Malignant tumor of colon NTNG1 22854 netrin G1 Q9Y2I2
C0085584 Encephalopathies NTNG1 22854 netrin G1 Q9Y2I2
C0036341 Schizophrenia NTNG1 22854 netrin G1 Q9Y2I2
C0013274 Patent ductus arteriosus NTNG1 22854 netrin G1 Q9Y2I2
C0600427 Cocaine Dependence NTNG1 22854 netrin G1 Q9Y2I2
C0009402 Colorectal Carcinoma NTNG1 22854 netrin G1 Q9Y2I2
C0014544 Epilepsy NTNG1 22854 netrin G1 Q9Y2I2
C0003125 Anorexia Nervosa NTNG1 22854 netrin G1 Q9Y2I2
C1384666 hearing impairment NTNG1 22854 netrin G1 Q9Y2I2
C1168401 Squamous cell carcinoma of the head and neck NTNG1 22854 netrin G1 Q9Y2I2
C0035372 Rett Syndrome NTNG1 22854 netrin G1 Q9Y2I2
C2748910 Rett Syndrome, Atypical NTNG1 22854 netrin G1 Q9Y2I2
C0442874 Neuropathy NTNG1 22854 netrin G1 Q9Y2I2
C0027651 Neoplasms NTNG1 22854 netrin G1 Q9Y2I2
C0005587 Depression, Bipolar NTNG1 22854 netrin G1 Q9Y2I2
C4282128 PATENT DUCTUS ARTERIOSUS 1 NTNG1 22854 netrin G1 Q9Y2I2
C3714756 Intellectual Disability NTNG1 22854 netrin G1 Q9Y2I2
C1531647 Cerebral ventriculomegaly NTNG1 22854 netrin G1 Q9Y2I2
C0009404 Colorectal Neoplasms NTNG1 22854 netrin G1 Q9Y2I2

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Last updated: August 19, 2024