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 |
---|---|---|---|---|---|
C0027051 | Myocardial Infarction | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0152018 | Esophageal carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0235974 | Pancreatic carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0006826 | Malignant Neoplasms | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0020538 | Hypertensive disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C1956346 | Coronary Artery Disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C2239176 | Liver carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0085762 | Alcohol abuse | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C1306459 | Primary malignant neoplasm | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0036341 | Schizophrenia | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0023895 | Liver diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0546837 | Malignant neoplasm of esophagus | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0376670 | Pancreatitis, Alcoholic | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0009402 | Colorectal Carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0279626 | Squamous cell carcinoma of esophagus | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0002395 | Alzheimer's Disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0018798 | Congenital Heart Defects | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0271650 | Impaired glucose tolerance | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0023530 | Leukopenia | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0007222 | Cardiovascular Diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0011884 | Diabetic Retinopathy | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0004096 | Asthma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0004352 | Autistic Disorder | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0853193 | Bipolar I disorder | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0000768 | Congenital Abnormality | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
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