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 3851 - 3875 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0018801 Heart failure SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0282160 Aplasia Cutis Congenita SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0699885 Carcinoma of bladder SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0600139 Prostate carcinoma SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0040136 Thyroid Neoplasm SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0004364 Autoimmune Diseases SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0750952 Biliary Tract Cancer SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0001430 Adenoma SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0007847 Malignant tumor of cervix SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0005695 Bladder Neoplasm SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0033860 Psoriasis SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0235782 Gallbladder Carcinoma SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0079731 B-Cell Lymphomas SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0235974 Pancreatic carcinoma SPHK1 8877 sphingosine kinase 1 Q9NYA1
C0033860 Psoriasis VNN1 8876 vanin 1 O95497
C0025517 Metabolic Diseases VNN1 8876 vanin 1 O95497
C0015624 Fanconi Syndrome VNN1 8876 vanin 1 O95497
C1306459 Primary malignant neoplasm VNN1 8876 vanin 1 O95497
C0009402 Colorectal Carcinoma VNN1 8876 vanin 1 O95497
C0178664 Glomerulosclerosis (disorder) VNN1 8876 vanin 1 O95497
C0149939 Obstructive nephropathy VNN1 8876 vanin 1 O95497
C0004153 Atherosclerosis VNN1 8876 vanin 1 O95497
C0699790 Colon Carcinoma VNN1 8876 vanin 1 O95497
C0020538 Hypertensive disease VNN1 8876 vanin 1 O95497
C0041956 Ureteral obstruction VNN1 8876 vanin 1 O95497

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Last updated: August 19, 2024