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 |
---|---|---|---|---|---|
C0035334 | Retinitis Pigmentosa | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0017531 | Angiolymphoid hyperplasia | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0027651 | Neoplasms | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0020615 | Hypoglycemia | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0024299 | Lymphoma | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0036220 | Kaposi Sarcoma | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C1334815 | Multi-centric Castleman's Disease | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0024314 | Lymphoproliferative Disorders | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0013336 | Dwarfism | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0021051 | Immunologic Deficiency Syndromes | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0027721 | Lipoid nephrosis | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C2711227 | Steatohepatitis | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0220981 | Metabolic acidosis | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0020258 | Hydrocephalus, Normal Pressure | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0001125 | Acidosis, Lactic | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0400966 | Non-alcoholic Fatty Liver Disease | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0687120 | Nephronophthisis | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0015695 | Fatty Liver | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0339277 | Corneal Dystrophy, Juvenile Epithelial of Meesmann | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0265289 | Metaphyseal chondrodysplasia Schmid type | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0041323 | Tuberculosis, Oral | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C0878544 | Cardiomyopathies | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
C1636149 | Macular dystrophy, corneal type 1 | MLYCD | 23417 | malonyl-CoA decarboxylase | O95822 |
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