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 351 - 375 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0011860 Diabetes Mellitus, Non-Insulin-Dependent HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0005283 beta Thalassemia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0024790 Paroxysmal nocturnal hemoglobinuria HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0349788 Arrhythmogenic Right Ventricular Dysplasia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0006826 Malignant Neoplasms HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C1621958 Glioblastoma Multiforme HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0005745 Blepharoptosis HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0400966 Non-alcoholic Fatty Liver Disease HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0020224 Polyhydramnios HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C3669246 Mammary adenocarcinoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0039730 Thalassemia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0003811 Cardiac Arrhythmia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0575158 Kyphoscoliosis deformity of spine HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C2711227 Steatohepatitis HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0021400 Influenza HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0020179 Huntington Disease HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0013336 Dwarfism HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C2239176 Liver carcinoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0017636 Glioblastoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0205969 Thymic Carcinoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0239946 Fibrosis, Liver HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0686353 Muscular Dystrophies, Limb-Girdle HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0014544 Epilepsy HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0333875 High-Grade Squamous Intraepithelial Lesions HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0042769 Virus Diseases HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81

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