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 1951 - 1975 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0175697 Van der Woude syndrome UMOD 7369 uromodulin P07911
C0175697 Van der Woude syndrome PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0175697 Van der Woude syndrome CYP2E1 1571 cytochrome P450 family 2 subfamily E member 1 P05181
C0175697 Van der Woude syndrome PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C0175697 Van der Woude syndrome PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C0175697 Van der Woude syndrome PRKAA2 5563 protein kinase AMP-activated catalytic subunit alpha 2 P54646
C0175697 Van der Woude syndrome PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0175697 Van der Woude syndrome CNTN2 6900 contactin 2 Q02246
C0432272 Van Buchem disease CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0042267 Vaginitis GLA 2717 galactosidase alpha P06280
C0042258 Vaginal Neoplasms SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0042258 Vaginal Neoplasms FH 2271 fumarate hydratase P07954
C1631597 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) THEM5 284486 thioesterase superfamily member 5 Q8N1Q8
C1631597 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) CNTN3 5067 contactin 3 Q9P232
C1876172 VAH, AUTOSOMAL RECESSIVE CFC1 55997 cripto, FRL-1, cryptic family 1 P0CG37
C1848599 VACTERL Association With Hydrocephalus PTEN 5728 phosphatase and tensin homolog P60484
C4554007 Uveoretinal Coloboma ALDH7A1 501 aldehyde dehydrogenase 7 family member A1 P49419
C0042170 Uveomeningoencephalitic Syndrome RPE 6120 ribulose-5-phosphate-3-epimerase Q96AT9
C0042170 Uveomeningoencephalitic Syndrome CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0042170 Uveomeningoencephalitic Syndrome CYP24A1 1591 cytochrome P450 family 24 subfamily A member 1 Q07973
C0042170 Uveomeningoencephalitic Syndrome CLEC16A 23274 C-type lectin domain containing 16A Q2KHT3
C0042167 Uveitis, Posterior ACE 1636 angiotensin I converting enzyme P12821
C0042167 Uveitis, Posterior ICAM1 3383 intercellular adhesion molecule 1 P05362
C0042166 Uveitis, Intermediate PTEN 5728 phosphatase and tensin homolog P60484
C0042164 Uveitis EXTL3 2137 exostosin like glycosyltransferase 3 O43909

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