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 9726 - 9750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
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
C0035334 Retinitis Pigmentosa ACOX1 51 acyl-CoA oxidase 1 Q15067
C0028738 Nystagmus ACOX1 51 acyl-CoA oxidase 1 Q15067
C0009402 Colorectal Carcinoma ACOX1 51 acyl-CoA oxidase 1 Q15067
C0006142 Malignant neoplasm of breast ACOX2 8309 acyl-CoA oxidase 2 Q99424
C4310624 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6 ACOX2 8309 acyl-CoA oxidase 2 Q99424
C0678222 Breast Carcinoma ACOX2 8309 acyl-CoA oxidase 2 Q99424
C0206624 Hepatoblastoma ACOX2 8309 acyl-CoA oxidase 2 Q99424
C0043459 Zellweger Syndrome ACOX2 8309 acyl-CoA oxidase 2 Q99424
C2239176 Liver carcinoma ACOX2 8309 acyl-CoA oxidase 2 Q99424
C1458155 Mammary Neoplasms ACOX2 8309 acyl-CoA oxidase 2 Q99424
C0007222 Cardiovascular Diseases ACOX2 8309 acyl-CoA oxidase 2 Q99424
C0038238 Steatorrhea ACOX2 8309 acyl-CoA oxidase 2 Q99424
C0600139 Prostate carcinoma ACOX3 8310 acyl-CoA oxidase 3, pristanoyl O15254
C0033578 Prostatic Neoplasms ACOX3 8310 acyl-CoA oxidase 3, pristanoyl O15254
C0376358 Malignant neoplasm of prostate ACOX3 8310 acyl-CoA oxidase 3, pristanoyl O15254

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Last updated: August 19, 2024