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 9501 - 9525 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0020538 Hypertensive disease ACO1 48 aconitase 1 P21399
C3150651 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 ACO1 48 aconitase 1 P21399
C0600139 Prostate carcinoma ACO2 50 aconitase 2 Q99798
C0699791 Stomach Carcinoma ACO2 50 aconitase 2 Q99798
C0854723 Retinal Dystrophies ACO2 50 aconitase 2 Q99798
C3281192 INFANTILE CEREBELLAR-RETINAL DEGENERATION ACO2 50 aconitase 2 Q99798
C3887709 Optic Neuropathy ACO2 50 aconitase 2 Q99798
C0028738 Nystagmus ACO2 50 aconitase 2 Q99798
C0027651 Neoplasms ACO2 50 aconitase 2 Q99798
C0006142 Malignant neoplasm of breast ACO2 50 aconitase 2 Q99798
C0010346 Crohn Disease ACO2 50 aconitase 2 Q99798
C0524851 Neurodegenerative Disorders ACO2 50 aconitase 2 Q99798
C0026650 Movement Disorders ACO2 50 aconitase 2 Q99798
C0740457 Malignant neoplasm of kidney ACO2 50 aconitase 2 Q99798
C0005586 Bipolar Disorder ACO2 50 aconitase 2 Q99798
C4225384 OPTIC ATROPHY 9 ACO2 50 aconitase 2 Q99798
C0376358 Malignant neoplasm of prostate ACO2 50 aconitase 2 Q99798
C0006826 Malignant Neoplasms ACO2 50 aconitase 2 Q99798
C1306459 Primary malignant neoplasm ACO2 50 aconitase 2 Q99798
C0038379 Strabismus ACO2 50 aconitase 2 Q99798
C0155016 Color Blindness, Red-Green ACO2 50 aconitase 2 Q99798
C0029124 Optic Atrophy ACO2 50 aconitase 2 Q99798
C0036572 Seizures ACO2 50 aconitase 2 Q99798
C1856689 FRIEDREICH ATAXIA 1 ACO2 50 aconitase 2 Q99798
C0035222 Respiratory Distress Syndrome, Adult ACO2 50 aconitase 2 Q99798

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Last updated: August 19, 2024