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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3351 - 3375** of **4621** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism
DOID:10541	microinvasive gastric cancer Aliases: Surface gastric cancer early gastric cancer	ACE CD44 CEACAM5 CEACAM7 FASN L1CAM MDGA2 PTEN PTGS2 SMUG1	1048 1087 161357 1636 2194 23583 3897 5728 5743 960	Homo sapiens (human)
DOID:8970	subacute sclerosing panencephalitis Aliases: Immunosuppressive measles encephalitis Van Bogaert's sclerosing leukoencephalitis subacute sclerosing leukoencephalopathy	ACE CD38 GLO1 PGM3 SDC1	1636 2739 5238 6382 952	Homo sapiens (human)
DOID:5485	synovial sarcoma	ACE CD38 ENO2 GLB1 GLO1 HPSE NANS PC PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 SELE SIRT2 SLC3A1 SMUG1 VCAM1 VTCN1	10855 1636 2026 22933 23583 2720 2739 5091 5290 5291 5293 5294 54187 5728 5743 6401 6519 7412 79679 952	Homo sapiens (human)
DOID:4386	myofibroma Aliases: Lipoleiomyoma	ACE CD38 CD44 CHST3 COG5 COG6 COMT CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP24A1 CYP2B6 CYP4F3 DHCR24 EBP EDEM2 ENO1 FASN FH FMOD GLB1 HK3 HPGDS HPSE2 HSD17B1 HSD17B2 HSD17B7 IL18R1 LGALS3 OGG1 PGAM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B POGLUT3 PTEN PTGS2 RECK SDHB SLC2A4 SMUG1 SORD TKTL1 UGT1A8 VCAN	10466 10682 1312 143888 1462 1543 1545 1555 1586 1588 1591 1636 1718 2023 2194 2271 2331 23583 2720 27306 3101 3292 3294 3958 4051 4968 51478 5223 5290 5291 5293 5294 5319 54576 55741 5728 5743 57511 60495 6390 6517 6652 8277 8434 8809 9469 952 960	Homo sapiens (human)
DOID:0080599	Coronavirus infectious disease	ACE CD209 MBL2 SFTPD	1636 30835 4153 6441	Homo sapiens (human)
DOID:3042	allergic contact dermatitis	ACE CD1D CNTN3 CYP1A1 ELOVL6 FCGR3B HSD11B1 MRC1 NAMPT SDC1 SELE SLC2A3 ST6GAL1 TLR4 UPP1	10135 1543 1636 2215 3290 4360 5067 6382 6401 6480 6515 7099 7378 79071 912	Homo sapiens (human)
DOID:10780	primary polycythemia Aliases: Familiar Polycythemia familial erythrocytosis	ACE CD177 FCER2 PKLR SLC17A5	1636 2208 26503 5313 57126	Homo sapiens (human)
DOID:0080033	craniometaphyseal dysplasia	ACE CD177 CHKB DAG1 FKRP FKTN IGF2R LGALS4 MPI POMT1 POMT2 ST3GAL4	10585 1120 1605 1636 2218 29954 3482 3960 4351 57126 6484 79147	Homo sapiens (human)
DOID:4331	burning mouth syndrome Aliases: Orodynia Stomatopyrosis	ACE CD14	1636 929	Homo sapiens (human)
DOID:4483	rhinitis	ACE CD14 HPGDS ICAM1 IL1RL1 LEP MBL2 PGP PTGDS SFTPD SIGLEC7 ST8SIA4 TLR2 TLR6 TNF	10333 1636 27036 27306 283871 3383 3952 4153 5730 6441 7097 7124 7903 9173 929	Homo sapiens (human)
DOID:10310	viral meningitis	ACE CD14 ENO2 GALNS ICAM1 LTA4H MBL2 MRC1 OGG1 PARP1 SMUG1 TPI1 VCAM1	142 1636 2026 23583 2588 3383 4048 4153 4360 4968 7167 7412 929	Homo sapiens (human)
DOID:1273	respiratory syncytial virus infectious disease Aliases: RSV respiratory syncytial virus	ACE CD14 CHI3L1 FCGR3B GPI HPGDS ICAM1 IL18R1 ISYNA1 MICA NCAM1 PTGDS PTGIS PTGS2 SFTPA1 SFTPA2 SFTPC SFTPD SIGLEC1 SMPD1 STS TLR4	100507436 1116 1636 2215 27306 2821 3383 412 4684 51477 5730 5740 5743 6440 6441 653509 6609 6614 7099 729238 8809 929	Homo sapiens (human)
DOID:0050662	bestrophinopathy Aliases: autosomal recessive bestrophinopathy	ACE CAT SLC33A1	1636 847 9197	Homo sapiens (human)
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	ACE CAT PTGS2	1636 5743 847	Homo sapiens (human)
DOID:5855	anteroseptal myocardial infarction	ACE CAT LGALS3 SLC2A4	1636 3958 6517 847	Homo sapiens (human)
DOID:5845	anterolateral myocardial infarction	ACE CAT LGALS3 SLC2A4	1636 3958 6517 847	Homo sapiens (human)
DOID:0111412	exudative vitreoretinopathy 1 Aliases: EVR1	ACE CAT EPHX2 FCN2 HPSE ICAM1 LGALS1 MCAT PIK3CA PIK3CB PIK3CD PIK3CG PNPLA2 PSMD10 TM7SF2 TMED5	10855 1636 2053 2220 27349 3383 3956 50999 5290 5291 5293 5294 57104 5716 7108 847	Homo sapiens (human)
DOID:13025	retinopathy of prematurity Aliases: Retrolental fibroplasia premature retinopathy	ACE CAT EPHX2 FCN2 HPSE ICAM1 LGALS1 MCAT PIK3CA PIK3CB PIK3CD PIK3CG PNPLA2 PSMD10 TM7SF2 TMED5	10855 1636 2053 2220 27349 3383 3956 50999 5290 5291 5293 5294 57104 5716 7108 847	Homo sapiens (human)
DOID:2388	renal artery disease Aliases: renal vascular disease vascular disorder of kidney	ACE CAT CYP4A11	1579 1636 847	Homo sapiens (human)
DOID:12783	migraine without aura Aliases: common migraine	ACE CAT COMT DHCR24 ENO2 GFRA1 HPGDS PLAUR PNPLA6 TNF	10908 1312 1636 1718 2026 2674 27306 5329 7124 847	Homo sapiens (human)
DOID:3240	aspiration pneumonitis Aliases: Chemical pneumonitis Mendelson's Syndrome	ACE CAT CHAT PMM2	1103 1636 5373 847	Homo sapiens (human)
DOID:0050152	aspiration pneumonia	ACE CAT CHAT PMM2 TNF	1103 1636 5373 7124 847	Homo sapiens (human)
DOID:12971	hereditary spherocytosis Aliases: Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia	ACE CAT CD55 G6PD GAPDH HK1 PGK1 PTGS2 ST8SIA4 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UMPS	1604 1636 2539 2597 3098 5230 54575 54576 54577 54578 54657 54658 5743 7372 7903 847	Homo sapiens (human)
DOID:9719	neovascular inflammatory vitreoretinopathy Aliases: ADNIV Retinitis proliferans autosomal dominant neovascular inflammatory vitreoretinopathy proliferative vitreoretinopathy	ACE CAT CD44 DCN FMOD HPGDS HPRT1 ICAM1 LGALS1 LGALS3 LRP5 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G6 RPE	1634 1636 2331 27306 3251 3383 3956 3958 4041 5290 5291 5293 5294 6120 8398 847 960	Homo sapiens (human)
DOID:2733	skin atrophy Aliases: Atrophoderma Atrophy - skin atrophic condition of skin	ACE CAT CD44 DCN DHCR24 GPI PIK3CA PIK3CB	1634 1636 1718 2821 5290 5291 847 960	Homo sapiens (human)

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