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 48351 - 48375 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
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
C0018801 Heart failure CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0086543 Cataract CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0020473 Hyperlipidemia CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0678222 Breast Carcinoma CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0006826 Malignant Neoplasms CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0400966 Non-alcoholic Fatty Liver Disease CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0342788 Renal carnitine transport defect CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0027651 Neoplasms CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0003864 Arthritis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0231528 Myalgia CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0007097 Carcinoma CPT2 1376 carnitine palmitoyltransferase 2 P23786
C2239176 Liver carcinoma CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0239946 Fibrosis, Liver CPT2 1376 carnitine palmitoyltransferase 2 P23786
C2711227 Steatohepatitis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0268238 Triglyceride storage disease with ichthyosis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0030312 Pancytopenia CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0042769 Virus Diseases CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0155626 Acute myocardial infarction CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0004153 Atherosclerosis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0311335 Grand Mal Status Epilepticus CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0342751 Generalized glycogen storage disease of infants CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0220994 Hyperammonemia CPT2 1376 carnitine palmitoyltransferase 2 P23786

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Last updated: August 19, 2024