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 |
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 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024