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 62226 - 62250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0001787 Osteoporosis, Age-Related OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0751406 Post-Traumatic Osteoporosis OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C1306459 Primary malignant neoplasm OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0151744 Myocardial Ischemia OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C1956346 Coronary Artery Disease OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C2239176 Liver carcinoma OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0017638 Glioma OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0036421 Systemic Scleroderma OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0031485 Phenylketonurias OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0028754 Obesity OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0029456 Osteoporosis OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0006826 Malignant Neoplasms OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0011644 Scleroderma OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0010068 Coronary heart disease OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0010054 Coronary Arteriosclerosis OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0011860 Diabetes Mellitus, Non-Insulin-Dependent OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0027651 Neoplasms OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0751434 Classical phenylketonuria OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0002895 Anemia, Sickle Cell OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C0079731 B-Cell Lymphomas KDSR 2531 3-ketodihydrosphingosine reductase Q06136
C0040034 Thrombocytopenia KDSR 2531 3-ketodihydrosphingosine reductase Q06136
C0024301 Lymphoma, Follicular KDSR 2531 3-ketodihydrosphingosine reductase Q06136
C0026847 Spinal Muscular Atrophy KDSR 2531 3-ketodihydrosphingosine reductase Q06136
C0005818 Blood Platelet Disorders KDSR 2531 3-ketodihydrosphingosine reductase Q06136
C0002170 Alopecia KDSR 2531 3-ketodihydrosphingosine reductase Q06136

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Last updated: August 19, 2024