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 726 - 750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
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
C0005586 Bipolar Disorder NTNG1 22854 netrin G1 Q9Y2I2
C0392525 Nephrolithiasis NTNG1 22854 netrin G1 Q9Y2I2
C0038454 Cerebrovascular accident NTNG1 22854 netrin G1 Q9Y2I2
C0036572 Seizures NTNG1 22854 netrin G1 Q9Y2I2
C0025958 Microcephaly NTNG1 22854 netrin G1 Q9Y2I2
C0024713 Manic Disorder NTNG1 22854 netrin G1 Q9Y2I2
C0338831 Manic NTNG1 22854 netrin G1 Q9Y2I2
C0026650 Movement Disorders NTNG1 22854 netrin G1 Q9Y2I2
C0017168 Gastroesophageal reflux disease NTNG1 22854 netrin G1 Q9Y2I2
C0004352 Autistic Disorder NTNG1 22854 netrin G1 Q9Y2I2
C0020473 Hyperlipidemia INPP5F 22876 inositol polyphosphate-5-phosphatase F Q9Y2H2
C0006142 Malignant neoplasm of breast INPP5F 22876 inositol polyphosphate-5-phosphatase F Q9Y2H2

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Last updated: August 19, 2024