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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 **2426 - 2450** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:1474	aggressive periodontitis Aliases: juvenile periodontitis	ALOX5 CD14 CYP1A1 DGKA FCGR3B GLT6D1 IL1R1 MBL2 MMP25 PAFAH1B1 PTGS2 SELE SIGLEC5 SMPD3 VCAM1	1543 1606 2215 240 3554 360203 4153 5048 55512 5743 6401 64386 7412 8778 929	Homo sapiens (human)	DisGeNET
DOID:9893	periodontosis	ALOX5 CD14 CYP1A1 DGKA FCGR3B GLT6D1 IL1R1 MBL2 MMP25 PAFAH1B1 PTGS2 SELE SIGLEC5 SMPD3 VCAM1	1543 1606 2215 240 3554 360203 4153 5048 55512 5743 6401 64386 7412 8778 929	Homo sapiens (human)	DisGeNET DisGeNET
DOID:824	periodontitis Aliases: chronic pericementitis	ACACA ACE ALPP APRT CALR CAT CD14 CD1D CD38 CD44 CD74 CEACAM7 CHGA CYP1A1 CYP1B1 CYP2E1 DDOST DLD ENO1 ENO3 FCGR3B FCN2 FMOD GAD1 GGT1 GLT6D1 GPX1 HPGDS ICAM1 IL18R1 IL1R1 INPP5D KLRB1 MBL2 NAMPT NT5E OCRL PIK3CA PIK3CB PIK3CD PIK3CG PNP PPARA PTGDS PTGES2 PTGES3 PTGES PTGS2 RECK SELE SELL SFTPD SIGLEC5 SLC2A4 SLC33A1 SMC3 ST8SIA4 STS TNF TNFRSF10C VCAM1	10135 10728 1087 1113 1543 1545 1571 1636 1650 1738 2023 2027 2215 2220 2331 250 2571 2678 27306 2876 31 3383 353 3554 360203 3635 3820 412 4153 4860 4907 4952 5290 5291 5293 5294 5465 5730 5743 6401 6402 6441 6517 7124 7412 7903 80142 811 8434 847 8778 8794 8809 912 9126 9197 929 952 9536 960 972	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3388	periodontal disease Aliases: disease of supporting structures of teeth periodontium disorder	ACE ALOX5 AMY1A AMY1B AMY1C CAT CD14 FCGR3B GPNMB IL18R1 LGALS9 LYZ MBL2 PNP PTGS2 RECK SELL SLC2A4 SMPD1 VCAM1	10457 1636 2215 240 276 277 278 3965 4069 4153 4860 5743 6402 6517 6609 7412 8434 847 8809 929	Homo sapiens (human)	DisGeNET
DOID:0050452	mevalonic aciduria Aliases: Mevalonate Kinase Deficiency	ABO ACE CHIT1 COL9A2 FDFT1 GLA GLO1 GPX1 LGALS3 LPIN2 LYZ MICA PIK3CG PRNP STS TNF	100507436 1118 1298 1636 2222 2717 2739 28 2876 3958 4069 412 5294 5621 7124 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2987	familial mediterranean fever Aliases: FMF benign paroxysmal peritonitis	ABO ACE ADIPOQ CAT CHIT1 COL9A2 CYP3A4 FDFT1 GLA GLO1 GPX1 LGALS3 LPIN2 LYZ MICA PIK3CG PRNP STS TLR4	100507436 1118 1298 1576 1636 2222 2717 2739 28 2876 3958 4069 412 5294 5621 7099 847 9370 9663	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:11481	constrictive pericarditis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:1787	pericarditis	CAT LACC1 NT5E PMM2 SMUG1	144811 23583 4907 5373 847	Homo sapiens (human)	DisGeNET
DOID:118	pericardial effusion	ACADVL ACE ALG9 CAT GBA1 PMM2 PTGS2 SMUG1	1636 23583 2629 37 5373 5743 79796 847	Homo sapiens (human)	DisGeNET
DOID:2508	Takayasu's arteritis Aliases: Aortic arch arteritis Idiopathic aortitis Takayasu arteritis Takayasu's disease aortic arch syndrome	ABO ACE B3GAT1 CEL CHI3L1 CYP21A2 FCGR3B GBA3 GLA INPP4B KLRB1 MICA NAAA NT5E PARP9 PTEN SELP SLC27A5 SMUG1 TPI1 VCAM1	100507436 1056 10998 1116 1589 1636 2215 23583 27087 27163 2717 28 3820 4907 5728 57733 6403 7167 7412 83666 8821	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:12132	granulomatosis with polyangiitis Aliases: Necrotizing respiratory granulomatosis Wegener granulomatosis, formerly	ABO ACE B3GAT1 CEL CHI3L1 CYP21A2 FCGR3B GBA3 GLA INPP4B KLRB1 MICA NAAA NT5E PARP9 PTEN SELP SLC27A5 SMUG1 TPI1 VCAM1	100507436 1056 10998 1116 1589 1636 2215 23583 27087 27163 2717 28 3820 4907 5728 57733 6403 7167 7412 83666 8821	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:9810	polyarteritis nodosa	ABO ACE B3GAT1 CEL CHI3L1 CYP21A2 FCGR3B GBA3 GFRA1 GLA INPP4B KLRB1 MICA NAAA NT5E PARP9 PTEN SELP SLC27A5 SMUG1 TPI1 VCAM1	100507436 1056 10998 1116 1589 1636 2215 23583 2674 27087 27163 2717 28 3820 4907 5728 57733 6403 7167 7412 83666 8821	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9808	Goodpasture syndrome Aliases: anti-GBM disease anti-glomerular basement membrane disease	ABO ACE B3GAT1 CEL CHI3L1 CYP19A1 CYP21A2 FCGR3B GBA3 GLA INPP4B KLRB1 MICA NAAA NT5E PARP9 PTEN SELP SLC27A5 SMUG1 TPI1 VCAM1	100507436 1056 10998 1116 1588 1589 1636 2215 23583 27087 27163 2717 28 3820 4907 5728 57733 6403 7167 7412 83666 8821	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:11269	chronic apical periodontitis	ALOX5 CD14 ICAM1 SIRT2 SIRT6	22933 240 3383 51548 929	Homo sapiens (human)	DisGeNET
DOID:823	periapical periodontitis Aliases: Apical periodontitis	ALOX5 CD14 ICAM1 SIRT2 SIRT6	22933 240 3383 51548 929	Homo sapiens (human)	DisGeNET
DOID:4617	periapical granuloma Aliases: Apical granuloma	B3GAT1 ICAM1 LGALS1 PTGS2 SIRT2	22933 27087 3383 3956 5743	Homo sapiens (human)	DisGeNET
DOID:2562	suppurative periapical periodontitis Aliases: Apical abscess Dentoalveolar abscess Periapical abscess Suppurative apical periodontitis	CD44 ENPP1 NT5E	4907 5167 960	Homo sapiens (human)	DisGeNET DisGeNET
DOID:750	peptic ulcer disease Aliases: acute peptic ulcer with hemorrhage acute peptic ulcer with hemorrhage and perforation acute peptic ulcer without hemorrhage and without perforation	A4GNT ABO ACE CD14 CYP1A1 CYP1A2 CYP2C19 CYP2C8 CYP2C9 CYP2E1 FUT4 GGT1 LDHA PTGS1 PTGS2 SI	1543 1544 1557 1558 1559 1571 1636 2526 2678 28 3939 51146 5742 5743 6476 929	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:11615	penile cancer Aliases: Ca penis Penile Ca malignant Penile tumor malignant neoplasm of body of penis penile neoplasm	PIK3CA PIK3CB PIK3CD PIK3CG SMUG1	23583 5290 5291 5293 5294	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11624	penile benign neoplasm Aliases: Penile tumor neoplasm of penis	PIK3CA PIK3CB PIK3CD PIK3CG PTGES SMUG1	23583 5290 5291 5293 5294 9536	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:8616	Peyronie's disease Aliases: Induratio penis plastica Peyronie disease Peyronie's Fibromatosis	DCN LIPA PARP1	142 1634 3988	Homo sapiens (human)	DisGeNET
DOID:13477	balanitis xerotica obliterans Aliases: Penile Lichen Sclerosus	DCN LIPA PARP1	142 1634 3988	Homo sapiens (human)	DisGeNET
DOID:8738	leukoplakia of penis Aliases: Kraurosis of penis Penile Leukoplakia	INPP5E	56623	Homo sapiens (human)	DisGeNET
DOID:0060851	pemphigus vulgaris Aliases: familial pemphigus vulgaris	ACE CYP21A2 FCN2 MBL2 MRC1	1589 1636 2220 4153 4360	Homo sapiens (human)	DisGeNET DisGeNET
DOID:9182	pemphigus	ACE CAT CD1D CYP21A2 FCN2 MBL2 MRC1	1589 1636 2220 4153 4360 847 912	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources

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