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 5851 - 5875 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0001973 Alcoholic Intoxication, Chronic SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0019202 Hepatolenticular Degeneration SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0239946 Fibrosis, Liver SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0020532 Hypersplenism SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C1852197 MAJOR AFFECTIVE DISORDER 1 SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0344315 Depressed mood SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C4721610 Carcinoma, Ovarian Epithelial SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0376358 Malignant neoplasm of prostate SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0024141 Lupus Erythematosus, Systemic SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0206656 Embryonal Rhabdomyosarcoma SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0042769 Virus Diseases SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0085576 Iron-Refractory Iron Deficiency Anemia SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0003873 Rheumatoid Arthritis SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C1855179 CATARACT, ANTERIOR POLAR SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0598608 Hyperhomocysteinemia SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0031511 Pheochromocytoma SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C1140680 Malignant neoplasm of ovary SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0036489 Sea-Blue Histiocyte Syndrome SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0005695 Bladder Neoplasm SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0035235 Respiratory Syncytial Virus Infections SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0699790 Colon Carcinoma SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0007102 Malignant tumor of colon SMPD1 6609 sphingomyelin phosphodiesterase 1 P17405
C0005741 Blepharitis SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C3714756 Intellectual Disability SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0235833 Congenital diaphragmatic hernia SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7

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Last updated: August 19, 2024