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 53076 - 53100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
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
C0034013 Precocious Puberty SLC35A2 7355 solute carrier family 35 member A2 P78381
C0028738 Nystagmus SLC35A2 7355 solute carrier family 35 member A2 P78381
C0019196 Hepatitis C SLC35A2 7355 solute carrier family 35 member A2 P78381
C0019163 Hepatitis B SLC35A2 7355 solute carrier family 35 member A2 P78381
C0036857 Severe intellectual disability SLC35A2 7355 solute carrier family 35 member A2 P78381
C0015310 Exotropia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0022353 Neonatal Jaundice SLC35A2 7355 solute carrier family 35 member A2 P78381
C0002895 Anemia, Sickle Cell SLC35A2 7355 solute carrier family 35 member A2 P78381
C0038379 Strabismus SLC35A2 7355 solute carrier family 35 member A2 P78381
C0010964 Dandy-Walker Syndrome SLC35A2 7355 solute carrier family 35 member A2 P78381
C0005283 beta Thalassemia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0018784 Sensorineural Hearing Loss (disorder) SLC35A2 7355 solute carrier family 35 member A2 P78381
C1856251 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I SLC35A2 7355 solute carrier family 35 member A2 P78381

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Last updated: August 19, 2024