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 57326 - 57350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0346647 Malignant neoplasm of pancreas SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0033999 Pterygium SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0085413 Polycystic Kidney, Autosomal Dominant SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0038454 Cerebrovascular accident SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0235974 Pancreatic carcinoma SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0027765 nervous system disorder SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0678222 Breast Carcinoma SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0014070 Encephalomyelitis SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0036220 Kaposi Sarcoma SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0025202 melanoma SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0017638 Glioma SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C1527336 Sjogren's Syndrome SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0206062 Lung Diseases, Interstitial SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C1800706 Idiopathic Pulmonary Fibrosis SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0014556 Epilepsy, Temporal Lobe SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0007124 Noninfiltrating Intraductal Carcinoma SEMA7A 8482 semaphorin 7A (John Milton Hagen blood group) O75326
C0376358 Malignant neoplasm of prostate UGT2B11 10720 UDP glucuronosyltransferase family 2 member B11 O75310
C0345905 Intrahepatic Cholangiocarcinoma UGT2B11 10720 UDP glucuronosyltransferase family 2 member B11 O75310
C0948008 Ischemic stroke XYLB 9942 xylulokinase O75191
C0410174 Fukuyama Type Congenital Muscular Dystrophy FKTN 2218 fukutin O75072
C0003466 Anus, Imperforate FKTN 2218 fukutin O75072
C0521694 Atrophic retina FKTN 2218 fukutin O75072
C0265221 Walker-Warburg congenital muscular dystrophy FKTN 2218 fukutin O75072
C0006826 Malignant Neoplasms FKTN 2218 fukutin O75072
C0025362 Mental Retardation FKTN 2218 fukutin O75072

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Last updated: August 19, 2024