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 45426 - 45450 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0015674 Chronic Fatigue Syndrome CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0006114 Cerebral Edema CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0017924 Glycogen Storage Disease Type V CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0025517 Metabolic Diseases CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0020456 Hyperglycemia CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0751651 Mitochondrial Diseases CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0011860 Diabetes Mellitus, Non-Insulin-Dependent CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0027051 Myocardial Infarction CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0017921 Glycogen storage disease type II CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0241005 Creatine phosphokinase serum increased CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0003811 Cardiac Arrhythmia CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0019158 Hepatitis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0268596 Multiple Acyl Coenzyme A Dehydrogenase Deficiency CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0025958 Microcephaly CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0015934 Fetal Growth Retardation CPT2 1376 carnitine palmitoyltransferase 2 P23786
C3714581 Multicystic Dysplastic Kidney CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0018802 Congestive heart failure CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0014038 Encephalitis CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0027849 Neuroleptic Malignant Syndrome CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0016202 Flatfoot CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1263846 Attention deficit hyperactivity disorder CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1829703 Carnitine palmitoyl transferase 1A deficiency CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0007193 Cardiomyopathy, Dilated CPT2 1376 carnitine palmitoyltransferase 2 P23786
C0011849 Diabetes Mellitus CPT2 1376 carnitine palmitoyltransferase 2 P23786
C1531647 Cerebral ventriculomegaly CPT2 1376 carnitine palmitoyltransferase 2 P23786

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Last updated: August 19, 2024