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 40051 - 40075 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0014852 Esophageal Diseases CEACAM5 1048 CEA cell adhesion molecule 5 P06731
C0014852 Esophageal Diseases PLA2G15 23659 phospholipase A2 group XV Q8NCC3
C0014852 Esophageal Diseases HPGDS 27306 hematopoietic prostaglandin D synthase O60760
C0014852 Esophageal Diseases ACSS2 55902 acyl-CoA synthetase short chain family member 2 Q9NR19
C0014852 Esophageal Diseases CD44 960 CD44 molecule (Indian blood group) P16070
C0014850 Esophageal Atresia CEACAM5 1048 CEA cell adhesion molecule 5 P06731
C0014850 Esophageal Atresia CEACAM7 1087 CEA cell adhesion molecule 7 Q14002
C0014850 Esophageal Atresia PTEN 5728 phosphatase and tensin homolog P60484
C0014848 Esophageal Achalasia FUT3 2525 fucosyltransferase 3 (Lewis blood group) P21217
C0014848 Esophageal Achalasia AGA 175 aspartylglucosaminidase P20933
C0014848 Esophageal Achalasia CALR 811 calreticulin P27797
C0014848 Esophageal Achalasia GMPPA 29926 GDP-mannose pyrophosphorylase A Q96IJ6
C0014848 Esophageal Achalasia ECI1 1632 enoyl-CoA delta isomerase 1 P42126
C0162568 Erythropoietic Protoporphyria SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0014804 Erythromelalgia PTGS1 5742 prostaglandin-endoperoxide synthase 1 P23219
C1851481 Erythrokeratodermia with ataxia ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0265961 Erythrokeratodermia variabilis ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0265961 Erythrokeratodermia variabilis KDSR 2531 3-ketodihydrosphingosine reductase Q06136
C4551637 Erythrocytosis familial, 1 PKLR 5313 pyruvate kinase L/R P30613
C0014761 Erythroblastosis, Fetal ABO 28 ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase P16442
C0014761 Erythroblastosis, Fetal OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0014742 Erythema Multiforme MASP2 10747 mannan binding lectin serine peptidase 2 O00187
C0014742 Erythema Multiforme FOLR2 2350 folate receptor beta P14207
C0014742 Erythema Multiforme FOLR1 2348 folate receptor alpha P15328
C0014742 Erythema Multiforme PLA2G15 23659 phospholipase A2 group XV Q8NCC3

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Last updated: August 19, 2024