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 39651 - 39675 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
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
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma NUDT5 11164 nudix hydrolase 5 Q9UKK9
C1306459 Primary malignant neoplasm NUDT5 11164 nudix hydrolase 5 Q9UKK9
C0006826 Malignant Neoplasms NUDT5 11164 nudix hydrolase 5 Q9UKK9
C0027651 Neoplasms NUDT5 11164 nudix hydrolase 5 Q9UKK9
C0006142 Malignant neoplasm of breast NUDT5 11164 nudix hydrolase 5 Q9UKK9
C0339535 Night blindness, congenital stationary NYX 60506 nyctalopin Q9GZU5
C1848172 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A NYX 60506 nyctalopin Q9GZU5
C0038379 Strabismus NYX 60506 nyctalopin Q9GZU5
C0028077 Nyctalopia NYX 60506 nyctalopin Q9GZU5
C3495587 Night Blindness, Congenital Stationary, Type 1A NYX 60506 nyctalopin Q9GZU5
C0035309 Retinal Diseases NYX 60506 nyctalopin Q9GZU5
C0007682 CNS disorder NYX 60506 nyctalopin Q9GZU5
C0027092 Myopia NYX 60506 nyctalopin Q9GZU5
C0023418 leukemia NYX 60506 nyctalopin Q9GZU5
C0152200 Achromatopsia NYX 60506 nyctalopin Q9GZU5
C0015397 Disorder of eye NYX 60506 nyctalopin Q9GZU5
C0028738 Nystagmus NYX 60506 nyctalopin Q9GZU5

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Last updated: August 19, 2024