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 46976 - 47000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0344315 Depressed mood ACOX1 51 acyl-CoA oxidase 1 Q15067
C0524851 Neurodegenerative Disorders ACOX1 51 acyl-CoA oxidase 1 Q15067
C0011581 Depressive disorder ACOX1 51 acyl-CoA oxidase 1 Q15067
C0751651 Mitochondrial Diseases ACOX1 51 acyl-CoA oxidase 1 Q15067
C0020608 Hypodontia ACOX1 51 acyl-CoA oxidase 1 Q15067
C1863844 Adult-onset citrullinemia type 2 ACOX1 51 acyl-CoA oxidase 1 Q15067
C0036857 Severe intellectual disability ACOX1 51 acyl-CoA oxidase 1 Q15067
C0023520 Leukodystrophy ACOX1 51 acyl-CoA oxidase 1 Q15067
C0345904 Malignant neoplasm of liver ACOX1 51 acyl-CoA oxidase 1 Q15067
C0011570 Mental Depression ACOX1 51 acyl-CoA oxidase 1 Q15067
C0279000 Liver and Intrahepatic Biliary Tract Carcinoma ACOX1 51 acyl-CoA oxidase 1 Q15067
C0027651 Neoplasms ACOX1 51 acyl-CoA oxidase 1 Q15067
C0038454 Cerebrovascular accident ACOX1 51 acyl-CoA oxidase 1 Q15067
C0027092 Myopia ACOX1 51 acyl-CoA oxidase 1 Q15067
C0037822 Speech Disorders ACOX1 51 acyl-CoA oxidase 1 Q15067
C0221356 Brachycephaly ACOX1 51 acyl-CoA oxidase 1 Q15067
C0154251 Lipid Metabolism Disorders ACOX1 51 acyl-CoA oxidase 1 Q15067
C0524620 Metabolic Syndrome X ACOX1 51 acyl-CoA oxidase 1 Q15067
C0018784 Sensorineural Hearing Loss (disorder) ACOX1 51 acyl-CoA oxidase 1 Q15067
C1332979 Childhood Lymphoma ACOX1 51 acyl-CoA oxidase 1 Q15067
C1332206 Adult Lymphoma ACOX1 51 acyl-CoA oxidase 1 Q15067
C0029124 Optic Atrophy ACOX1 51 acyl-CoA oxidase 1 Q15067
C0013421 Dystonia ACOX1 51 acyl-CoA oxidase 1 Q15067
C0024299 Lymphoma ACOX1 51 acyl-CoA oxidase 1 Q15067
C0038379 Strabismus ACOX1 51 acyl-CoA oxidase 1 Q15067

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Last updated: August 19, 2024