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 9676 - 9700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C1636149 Macular dystrophy, corneal type 1 SLC35A2 7355 solute carrier family 35 member A2 P78381
C0002395 Alzheimer's Disease SLC35A2 7355 solute carrier family 35 member A2 P78381
C0002875 Cooley's anemia SLC35A2 7355 solute carrier family 35 member A2 P78381
C1527366 Salaam Seizures SLC35A2 7355 solute carrier family 35 member A2 P78381
C0014859 Esophageal Neoplasms SLC35A2 7355 solute carrier family 35 member A2 P78381
C0221023 Cyclic neutropenia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0152018 Esophageal carcinoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0013336 Dwarfism SLC35A2 7355 solute carrier family 35 member A2 P78381
C0003081 Anisometropia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0524620 Metabolic Syndrome X SLC35A2 7355 solute carrier family 35 member A2 P78381
C0400966 Non-alcoholic Fatty Liver Disease SLC35A2 7355 solute carrier family 35 member A2 P78381
C0857007 Hyperbilirubinemia, Neonatal SLC35A2 7355 solute carrier family 35 member A2 P78381
C4721610 Carcinoma, Ovarian Epithelial SLC35A2 7355 solute carrier family 35 member A2 P78381
C0376358 Malignant neoplasm of prostate SLC35A2 7355 solute carrier family 35 member A2 P78381
C0014877 Esotropia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0011226 Hepatitis D Infection SLC35A2 7355 solute carrier family 35 member A2 P78381
C0036572 Seizures SLC35A2 7355 solute carrier family 35 member A2 P78381
C0919267 ovarian neoplasm SLC35A2 7355 solute carrier family 35 member A2 P78381
C0034194 Pyloric Stenosis SLC35A2 7355 solute carrier family 35 member A2 P78381
C0271979 Thalassemia Intermedia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0600139 Prostate carcinoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0010278 Craniosynostosis SLC35A2 7355 solute carrier family 35 member A2 P78381
C4317295 Congenital disorder of glycosylation type 1s SLC35A2 7355 solute carrier family 35 member A2 P78381
C1140680 Malignant neoplasm of ovary SLC35A2 7355 solute carrier family 35 member A2 P78381
C1332206 Adult Lymphoma SLC35A2 7355 solute carrier family 35 member A2 P78381

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Last updated: August 19, 2024