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 57301 - 57325 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C1565489 Renal Insufficiency CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1833518 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0003872 Arthritis, Psoriatic CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1833508 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0021400 Influenza CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0220710 Medium-chain acyl-coenzyme A dehydrogenase deficiency CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0035410 Rhabdomyolysis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C3887523 Very long chain acyl-CoA dehydrogenase deficiency CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0600139 Prostate carcinoma CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0085584 Encephalopathies CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0878544 Cardiomyopathies CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0036572 Seizures CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0020615 Hypoglycemia CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0022661 Kidney Failure, Chronic CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1969443 Trifunctional Protein Deficiency With Myopathy And Neuropathy CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0026848 Myopathy CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0162323 Polyarthritis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C3203102 Idiopathic pulmonary arterial hypertension CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0006142 Malignant neoplasm of breast CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1449563 Cardiomyopathy, Familial Idiopathic CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0154251 Lipid Metabolism Disorders CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0015695 Fatty Liver CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0376358 Malignant neoplasm of prostate CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0028754 Obesity CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0009402 Colorectal Carcinoma CPT2 1376 carnitine palmitoyltransferase 2 P23786

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Last updated: August 19, 2024