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 201 - 225 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
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
C3714756 Intellectual Disability HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0010417 Cryptorchidism HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0376358 Malignant neoplasm of prostate HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0085669 Acute leukemia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0040100 Thymoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C1458155 Mammary Neoplasms HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0032285 Pneumonia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0270960 Congenital myopathy (disorder) HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0003175 Anthrax disease HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0007125 Carcinoma, Ehrlich Tumor HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0029089 Ophthalmoplegia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0038454 Cerebrovascular accident HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0004096 Asthma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C1332986 Childhood Osteosarcoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0024198 Lyme Disease HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0949570 Wheat Hypersensitivity HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0699791 Stomach Carcinoma HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0032460 Polycystic Ovary Syndrome HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0002874 Aplastic Anemia HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0175709 Centronuclear myopathy HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81
C0009081 Congenital clubfoot HACD1 9200 3-hydroxyacyl-CoA dehydratase 1 B0YJ81

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Last updated: August 19, 2024