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 39351 - 39375 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C1168401 Squamous cell carcinoma of the head and neck TKTL1 8277 transketolase like 1 P51854
C0028756 Obesity, Morbid TKTL1 8277 transketolase like 1 P51854
C0042133 Uterine Fibroids TKTL1 8277 transketolase like 1 P51854
C0007102 Malignant tumor of colon TKTL1 8277 transketolase like 1 P51854
C0600139 Prostate carcinoma TKTL1 8277 transketolase like 1 P51854
C0009402 Colorectal Carcinoma TKTL1 8277 transketolase like 1 P51854
C0017638 Glioma TKTL1 8277 transketolase like 1 P51854
C0006142 Malignant neoplasm of breast TKTL1 8277 transketolase like 1 P51854
C0001418 Adenocarcinoma TKTL1 8277 transketolase like 1 P51854
C0007097 Carcinoma TKTL1 8277 transketolase like 1 P51854
C0393591 AICARDI-GOUTIERES SYNDROME TKTL1 8277 transketolase like 1 P51854
C2931822 Nasopharyngeal carcinoma TKTL1 8277 transketolase like 1 P51854
C0023903 Liver neoplasms TKTL1 8277 transketolase like 1 P51854
C0023473 Myeloid Leukemia, Chronic TKTL1 8277 transketolase like 1 P51854
C0019159 Hepatitis A AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0000768 Congenital Abnormality AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0025517 Metabolic Diseases AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0024523 Malabsorption Syndrome AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0020433 Hyperbilirubinemia AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0400966 Non-alcoholic Fatty Liver Disease AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0023895 Liver diseases AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0029456 Osteoporosis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C1856127 Bile acid synthesis defect, congenital, 2 AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0392514 Hereditary hemochromatosis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857
C0003873 Rheumatoid Arthritis AKR1D1 6718 aldo-keto reductase family 1 member D1 P51857

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Last updated: August 19, 2024