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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 **4176 - 4200** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:227	ankylosis	ENPP1 PLCB4	5167 5332	Homo sapiens (human)	DisGeNET
DOID:12273	anisometropia	PTEN SLC35A2	5728 7355	Homo sapiens (human)	DisGeNET
DOID:12271	aniridia Aliases: Aplasia of iris isolated aniridia	ADH7 ARSD CAT CYP1B1 DLST FH GPC3 LDHD MDH2 SDHA SDHB SDHC SDHD	131 1545 1743 197257 2271 2719 414 4191 6389 6390 6391 6392 847	Homo sapiens (human)	DisGeNET
DOID:11156	anhidrosis Aliases: Adiaphoresis absence of sweating	ALOX12B CEACAM5 CERS3 COG6 CTNS ELOVL4 FUCA1 GAL3ST1 GLA HEXB NGLY1 SLC35A1 SPTLC2 STS	1048 10559 1497 204219 242 2517 2717 3074 412 55768 57511 6785 9514 9517	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11155	hypohidrosis Aliases: Oligohidrosis	ALOX12B CEACAM5 CERS3 COG6 CTNS ELOVL4 FUCA1 GAL3ST1 GLA HEXB NGLY1 SLC35A1 SPTLC2 STS	1048 10559 1497 204219 242 2517 2717 3074 412 55768 57511 6785 9514 9517	Homo sapiens (human)	DisGeNET DisGeNET
DOID:1558	angioedema Aliases: Angioneurotic oedema Quincke's edema angioneurotic edema giant urticaria	ABO ACE AGXT ALDH3A2 ALOX5 ARSA BST2 CAT CD38 DGKG ELOVL4 FCGR3B GPX1 HPGDS ICAM1 LTC4S MASP2 MBL2 PIGT PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLCG1 PLCG2 PTGS2 SDHB SDHC SELE SMUG1 VCAM1 XPNPEP2	10747 1608 1636 189 2215 224 23583 240 27306 28 2876 3383 4056 410 4153 51604 5290 5291 5293 5294 5321 5335 5336 5743 6390 6391 6401 6785 684 7412 7512 847 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:14735	hereditary angioedema Aliases: HANE Hereditary angioneurotic edema	ABO ACE HS3ST6 MASP2 MBL2 SMUG1 VCAM1 XPNPEP2	10747 1636 23583 28 4153 64711 7412 7512	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:14308	skin epithelioid hemangioma Aliases: Angiolymphoid Cutaneous hyperplasia epithelioid hemangioma of skin	LGALS9 SMUG1	23583 3965	Homo sapiens (human)	DisGeNET DisGeNET
DOID:7365	Kimura disease Aliases: Kimura's disease	CD48 FUT4 LGALS9 MLYCD SMUG1	23417 23583 2526 3965 962	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:9455	lipid storage disease Aliases: Lipoid storage diseas inborn lipid storage disorder lipoidosis	AGA ARSA ARSB ASAH1 CAT CEL CHIT1 CTSA CYP27A1 FADS2 G6PC1 G6PD GAA GALC GBA1 GBE1 GDPD3 GLA GLB1 GNPTAB GNPTG GUSB ICAM1 IDS IDUA LGALS3 LIPA LIPF LPL LSS MANBA MGAM NAGA NAGPA NCAM1 NT5E OGA PSAP PTGDS SCD SELE SFTPD SI SLC2A3 SMPD1 SMUG1 SOAT2 UGCG UGT1A1 UMOD VCAM1	1056 10724 1118 1593 175 23583 2538 2539 2548 2581 2629 2632 2717 2720 2990 3383 3423 3425 3958 3988 4023 4047 410 411 4126 427 4668 4684 4907 51172 54658 5476 5660 5730 6319 6401 6441 6476 6515 6609 7357 7369 7412 79153 79158 8435 84572 847 8513 8972 9415	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060357	chylomicron retention disease Aliases: Anderson disease CMRD	AGA AMT ARSA ARSB ASAH1 CHIT1 CTSA CYP27A1 DGAT1 FADS2 G6PC1 G6PD GAA GALC GBA1 GBE1 GDPD3 GLA GLB1 GNPTAB GNPTG GPIHBP1 GUSB ICAM1 IDS IDUA LCAT LGALS3 LPL LSS MANBA MGAM NAGA NAGPA NT5E OGA PNPLA2 PTGDS SCD SELE SFTPD SI SLC2A3 SMPD1 SMUG1 UGCG UGT1A1 UMOD VCAM1	10724 1118 1593 175 23583 2538 2539 2548 2581 2629 2632 2717 2720 275 2990 3383 338328 3423 3425 3931 3958 4023 4047 410 411 4126 427 4668 4907 51172 54658 5476 57104 5730 6319 6401 6441 6476 6515 6609 7357 7369 7412 79153 79158 84572 8694 8972 9415	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:479	angiokeratoma Aliases: Angiokeratoma of skin Cutaneous Angiokeratoma skin angiokeratoma	DCN FUCA1 GLA IDH1 IDH2 MANBA NAGA PTEN SMUG1	1634 23583 2517 2717 3417 3418 4126 4668 5728	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:13401	angioid streaks	ENPP1 GALNT3 PIK3CA PTEN XYLT1 XYLT2	2591 5167 5290 5728 64131 64132	Homo sapiens (human)	DisGeNET
DOID:8805	intermediate coronary syndrome Aliases: Angina at rest Anginal chest pain at rest Impending infarction Preinfarction angina Unstable angina Worsening angina	ACE AKT1 ARSA CD14 CHGA CHI3L1 CYP2C19 ICAM1 IL18R1 LGALS3 MBL2 PARP1 PLA2G1B PLB1 PTEN PTGS2 SELP SULT1E1	1113 1116 142 151056 1557 1636 207 3383 3958 410 4153 5319 5728 5743 6403 6783 8809 929	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0111151	Prinzmetal angina Aliases: Prinzmetal's angina Prinzmetal's variant angina angina inversa variant angina variant angina pectoris	ACE AKR1A1 ALDH2 ICAM1 KL PCYT1A SMUG1	10327 1636 217 23583 3383 5130 9365	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:178	vascular disease Aliases: vascular tissue disease	ABO ACE ACSL1 ADH1B ADIPOQ AKR1B1 ALDH2 CAT CD38 CHI3L1 CYP19A1 CYP2C9 CYP4F2 DCN DDOST DLAT DLD ENO2 FCGR3B FCN2 FOLR2 G6PD GLA GLO1 GPI HPSE ICAM1 ISYNA1 KL LGALS3 LIPC LIPG LPCAT3 LPL MBL2 NAMPT OLR1 PAFAH1B1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLA2G7 PLB1 PNP PRKAA2 PTEN PTGS2 RENBP SELE SELL SLC2A10 SLC2A4 SMUG1 SOAT1 SPHK2 TM7SF2 VCAM1 VCAN	10135 10162 10855 1116 125 1462 151056 1559 1588 1634 1636 1650 1737 1738 2026 217 2180 2215 2220 231 2350 23583 2539 2717 2739 28 2821 3383 3958 3990 4023 4153 4860 4973 5048 51477 5290 5291 5293 5294 5320 5563 56848 5728 5743 5973 6401 6402 6517 6646 7108 7412 7941 81031 847 8529 9365 9370 9388 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060668	anencephaly	ABO B4GAT1 COMT EFNA5	11041 1312 1946 28	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:8955	sideroblastic anemia Aliases: ANEMIA SIDEROBLASTIC Anemia, hypochromic with iron loading	CALR CYP2E1	1571 811	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia	ABO ACE ALOX5 ANXA5 CAT CD14 CD38 CD55 CHIT1 COMT CYB5R3 CYP2C19 FCGR3B FDPS FH FUCA2 FUT1 G6PD GAD1 GALNT13 GAPDH GPX1 HEXA HK1 HPGDS IMPA1 KL KLRC3 LCAT LFNG LGALS3 LIPG LPCAT1 LPCAT3 LYZ MBL2 NT5E OLR1 OXCT1 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PRNP SCD5 SCD SELE SELL SELP SFTPD SLC17A5 SLC35A2 SMPD1 SMUG1 TALDO1 TNF UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B7 UMPS VCAM1	10162 1118 114805 1312 1557 1604 1636 1727 2215 2224 2271 23583 240 2519 2523 2539 2571 2597 26503 27306 28 2876 3073 308 3098 3612 3823 3931 3955 3958 4069 4153 4907 4973 5019 5319 5320 5321 54575 54576 54577 54578 54579 54600 54657 54658 54659 5621 56886 6319 6401 6402 6403 6441 6609 6888 7124 7355 7364 7372 7412 79888 79966 8398 847 929 9365 9388 952	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:13381	pernicious anemia Aliases: ANEMIA PERNICIOUS Addison's anaemia Biermer's anaemia Biermer's anemia pernicious anaemia	FUT6 GAD2	2528 2572	Homo sapiens (human)	DisGeNET
DOID:11244	neonatal anemia Aliases: anaemia neonatal anemia neonatal neonatal anaemia	ABO GPI OCRL	28 2821 4952	Homo sapiens (human)	DisGeNET DisGeNET
DOID:13382	megaloblastic anemia Aliases: Grasbeck-Imerslund syndrome Imerslund-Grasbeck syndrome MGA1 Norwegian type RH-MGA1 megaloblastic anaemia recessive hereditary megaloblastic anaemia 1 recessive hereditary megaloblastic anemia 1	HPRT1 UMPS	3251 7372	Homo sapiens (human)	DisGeNET
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	G6PD GPI HK1 PKLR TPI1	2539 2821 3098 5313 7167	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2860	hemoglobinopathy Aliases: hemoglobinopathies	ABO ALDOA CD55 FUT1 G6PD GPI HK1 NT5E PKLR SCD TPI1 UGT1A1	1604 226 2523 2539 28 2821 3098 4907 5313 54658 6319 7167	Homo sapiens (human)	DisGeNET DisGeNET
DOID:2373	hereditary elliptocytosis Aliases: Congenital elliptocytosis ovalocytosis	ACSL4 ALDOA ALPL ALPP ATRNL1 CAT CD55 ENPP1 G6PD GPI HK1 NDUFAB1 PKLR TPI1 UGT8	1604 2182 226 249 250 2539 26033 2821 3098 4706 5167 5313 7167 7368 847	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET

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