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 ▼ |
---|---|---|---|---|---|
C0023212 | Left-Sided Heart Failure | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C1306459 | Primary malignant neoplasm | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0010068 | Coronary heart disease | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0005586 | Bipolar Disorder | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0014742 | Erythema Multiforme | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0346647 | Malignant neoplasm of pancreas | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0018802 | Congestive heart failure | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0220710 | Medium-chain acyl-coenzyme A dehydrogenase deficiency | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0015469 | Facial paralysis | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0022661 | Kidney Failure, Chronic | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0036572 | Seizures | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C2239176 | Liver carcinoma | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0036341 | Schizophrenia | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0014544 | Epilepsy | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0006826 | Malignant Neoplasms | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0036439 | Scoliosis, unspecified | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C1956346 | Coronary Artery Disease | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0878544 | Cardiomyopathies | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0033975 | Psychotic Disorders | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C1561643 | Chronic Kidney Diseases | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C1959583 | Myocardial Failure | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
C0023467 | Leukemia, Myelocytic, Acute | CBR1 | 873 | carbonyl reductase 1 | P16152 |
C1306459 | Primary malignant neoplasm | CBR1 | 873 | carbonyl reductase 1 | P16152 |
C0007097 | Carcinoma | CBR1 | 873 | carbonyl reductase 1 | P16152 |
C1621958 | Glioblastoma Multiforme | CBR1 | 873 | carbonyl reductase 1 | P16152 |
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