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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 **3076 - 3100** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
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)
DOID:0050793	short QT syndrome	CACNA2D1 KCNQ1	3784 781	Homo sapiens (human)
DOID:12859	choreatic disease Aliases: chorea hereditary chorea	ACAT2 ALG13 ARSA B3GALNT2 CACNA2D2 GM2A LMAN2L MAN1B1 MBOAT7 MECR MYORG NDST1 NGLY1 PGAP1 PIGC PLA2G6 PRNP PSAP SMUG1 ST3GAL3 TECR TUSC3	11253 148789 23583 2760 3340 39 410 51102 5279 55768 5621 5660 57462 6487 79143 79868 7991 80055 81562 8398 9254 9524	Homo sapiens (human)
DOID:0110307	hypertrophic cardiomyopathy 1 Aliases: CMH1 cardiomyopathy, familial hypertrophic 1 hypertrophic cardiomyopathy 19	ACE APRT CALR3 GLA GNS HGSNAT ICAM1 NAGLU PKD1 PNPLA3 PRKAA2 SGSH	125972 138050 1636 2717 2799 3383 353 4669 5310 5563 6448 80339	Homo sapiens (human)
DOID:0080546	non-alcoholic fatty liver Aliases: NAFL nonalcoholic fatty liver	GGT1 HTR2A	2678 3356	Homo sapiens (human)
DOID:0111390	mucopolysaccharidosis Ih Aliases: Dysostosis multiplex syndrome Hurler disease MPS type 1H Hurler-Pfaundler syndrome L-iduronidase deficiency, Hurler type MPS1-H Mucopolysaccharidosis type I severe form dysostosis multiplex gargoylism	AGA ARSB CAT CTSA FUCA1 FUT1 GLB1 GNE GNPTAB GNPTG GNS GUSB HGSNAT IDS IDUA MAN2B1 NAGLU NEU1 SGSH SUMF1	10020 138050 175 2517 2523 2720 2799 285362 2990 3423 3425 411 4125 4669 4758 5476 6448 79158 84572 847	Homo sapiens (human)
DOID:11123	Henoch-Schoenlein purpura Aliases: Allergic purpura Autoimmune purpura Henoch-Sch?nlein purpura Henoch-Sch@nlein purpura Henoch-Scholein purpura Henoch-Schonlein Purpura Purpura, autoimmune	ACE B4GALNT1 C1GALT1 CPT1C CYP19A1 CYP2U1 CYP7B1 GBA2 ICAM1 L1CAM MBL2 MGAT5 NAAA PARP1 PLA2G6 PLD3 PNPLA6 SLC33A1	10908 113612 126129 142 1588 1636 23646 2583 27163 3383 3897 4153 4249 56913 57704 8398 9197 9420	Homo sapiens (human)
DOID:5845	anterolateral myocardial infarction	ACE CAT LGALS3 SLC2A4	1636 3958 6517 847	Homo sapiens (human)
DOID:0110533	autosomal recessive nonsyndromic deafness 88 Aliases: DFNB88 autosomal recessive deafness 88	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:345	uterine disease	AKR1C2 CYP19A1 HSD17B1	1588 1646 3292	Homo sapiens (human)
DOID:0070257	congenital disorder of glycosylation type IIe Aliases: CDG IIe CDG syndrome type IIe CDG2E CDGIIde COG7-CDG Carbohydrate deficient glycoprotein syndrome type IIe	COG7	91949	Homo sapiens (human)
DOID:5825	adult lymphoma	ABO ACE ACOX1 ACSF3 ALOX12 ALOX15 ALPI ALPP ANXA5 CALR CAT CD14 CD1D CD22 CD33 CD38 CD44 CD48 CD55 CD74 CEL CHGA CLEC10A CNTN2 COMT CYP17A1 CYP1A1 CYP2B6 DGKZ ENO2 ENOSF1 EPM2A FCER2 FCGR3B FH FMOD G6PD GBA1 GLB1 GPI GPX1 HEXA HMMR HPGDS HPSE HS3ST2 HYAL2 ICAM1 IDH1 IDH2 IL1R1 IL1RL1 INPP4B INPP5D ISYNA1 KLRC1 KLRD1 KLRK1 LGALS1 LGALS3 LY6K MBL2 MCAT MLYCD MRC1 MTAP NCAM1 NDUFAB1 NT5E PARP9 PIGK PIK3CA PIK3CB PIK3CD PIK3CG PNP PPP1R3A PTEN PTGDS PTGES PTGS2 RTN4R SELE SGPP1 SLC27A5 SLC2A3 SLC35A2 SLC35B2 SMC3 SMUG1 SOAT1 SPHK2 STS SULT1E1 TIGAR TMTC3 TNFRSF10C ULBP1 VCAM1 VTCN1	10026 10462 1056 10855 10998 1113 1312 1543 1555 1586 1604 160418 1636 197322 2026 2208 2215 2271 22914 2331 23417 23583 239 246 248 250 2539 2629 2720 27306 27349 28 2821 2876 3073 308 3161 3383 3417 3418 347734 3554 3635 3821 3824 3956 3958 412 4153 4360 4507 4684 4706 4860 4907 51 51477 5290 5291 5293 5294 54742 5506 55556 56848 57103 5728 5730 5743 6401 65078 6515 6646 6783 6900 7355 7412 7957 79679 80329 811 81537 83666 847 8525 8692 8794 8821 912 9126 9173 929 933 945 952 9536 960 962 972 9956	Homo sapiens (human)
DOID:0110820	hereditary spastic paraplegia 75 Aliases: SPG75 autosomal recessive spastic paraplegia 75 autosomal recessive spastic paraplegia type 75	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:8677	perinatal necrotizing enterocolitis Aliases: ENTEROCOLITIS NECROTIZING Necrotizing enterocolitis in fetus OR newborn Perinatal necrotising enterocolitis Pseudomembranous enterocolitis in newborn necrotizing enterocolitis	ABO ACACB ACADM ACE AKR1A1 ALDH2 CAT CD14 CRYL1 ENO1 FCN1 GM2A ICAM1 LGALS2 MBL2 NCAM1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLAUR PTGS2 SELE SELL SFTPC SORD TLR1 TLR2 TLR4 TLR6 TNF	10327 10333 142 1636 2023 217 2219 2760 28 32 3383 34 3957 4153 4684 51084 5290 5291 5293 5294 5329 5743 6401 6402 6440 6652 7096 7097 7099 7124 847 929	Homo sapiens (human)
DOID:0110225	Brugada syndrome 8 Aliases: BRGDA8	APRT CACNA2D1 GPD1L IDS SCD	23171 3423 353 6319 781	Homo sapiens (human)
DOID:784	chronic kidney disease Aliases: CKD CRF chronic kidney failure chronic renal disease chronic renal failure syndrome renal failure - chronic	ABO ACACA ACADL ACADS ACAT1 ACE ACHE ACLY ACSBG1 ACSM3 ACSS2 AGXT AKR1B1 ALDH2 ALDOB AMACR ANXA5 APRT ARSA ATP6AP2 B3GAT1 CAT CBR1 CD14 CD177 CD248 CD55 CDH13 CERS2 CERS4 CHGA CHI3L1 CLEC16A CMAS CNTN3 COL9A2 COMT CPT1A CPT2 CYP11B2 CYP1A1 CYP1A2 CYP24A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP3A4 CYP3A5 DDOST DGAT1 DGAT2 DHCR24 DPEP1 ENO1 ENPP1 EPHX2 EXTL2 FADS1 FADS2 FAR2 FASN FCGR3B G6PC1 GAD1 GALNT3 GFPT2 GGT1 GLA GLB1 GPX1 GPX3 GRHPR HJV HOGA1 HPGDS HPSE HSD11B1 HSD11B2 ICAM1 IGF2R KL LCAT LEPR LGALS3 LIPC LPIN1 LPL MANBA MBL2 MBOAT7 MICA MPI MTM1 NAGLU NAMPT OCRL OGA OGG1 OLR1 PARP1 PCYT1A PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1B PKD1 PKD2 PLA2G10 PLA2G15 PLA2G2A PLA2R1 PLB1 PLCE1 PLD1 PLD2 PNPLA3 PRKAA2 PRNP PTGDS PTGES PTGS1 PTGS2 RBP4 RENBP RGMA RPN1 SDC1 SELE SELL SELP SFTPA1 SHMT1 SIRT6 SLC17A5 SLC2A4 SLC33A1 SLC3A1 SMPD3 SMUG1 SPHK2 ST8SIA4 STS TALDO1 TKT UMOD VCAM1 VCAN VNN1 XYLT2	100507436 1012 10135 10159 10724 10855 1113 1116 112817 1298 1312 1374 1376 142 1462 148738 151056 1543 1544 1555 1557 1558 1559 1576 1577 1585 1591 1594 1604 1636 1650 1718 1800 189 2023 2053 2135 217 2194 2215 229 22925 231 23175 23205 23274 23583 23600 23659 2538 2571 2591 26503 2678 27087 2717 2720 27306 28 2876 2878 29956 308 31 3290 3291 33 3383 3482 35 353 38 3931 3953 3958 3990 3992 4023 410 412 4126 4153 43 4351 4534 4669 47 4952 4968 4973 5067 51196 5130 51548 5167 5289 5290 5291 5293 5294 5310 5311 5320 5337 5338 55512 5563 55711 55902 55907 5621 56848 56963 57124 57126 5730 5742 5743 5950 5973 6184 6296 6382 6401 6402 6403 64132 6470 6517 6519 653509 6888 7086 7369 7412 7903 79143 79603 80339 8395 8399 84649 847 8694 873 8876 9197 929 9365 9380 9415 9536 9945	Homo sapiens (human)
DOID:0110915	childhood hypophosphatasia	ALPL	249	Homo sapiens (human)
DOID:999	hypereosinophilic syndrome Aliases: Eosinophilic leukocytosis eosinophilia	ACOT7 CD1D CEL CLEC10A CYP2C19 ETNK1 EXTL3 HPGDS HS2ST1 HSPG2 ICAM1 IL18R1 IL1RL1 LGALS9 LPCAT1 MBL2 NDST1 PARP1 PARP9 PGM3 PLA2G5 PTEN PTGDS PTGS2 SDC2 SELL SFTPA2 SFTPD SIGLEC8 SLC27A5 TNFRSF10C VCAM1	10462 1056 10998 11332 142 1557 2137 27181 27306 3339 3340 3383 3965 4153 5238 5322 55500 5728 5730 5743 6383 6402 6441 729238 7412 79888 83666 8794 8809 912 9173 9653	Homo sapiens (human)
DOID:1394	urinary schistosomiasis Aliases: Schistosoma Hematobium Infection Schistosoma haematobium Schistosoma hematobium infectious disease Schistosomiasis due to schistosoma haematobium Schistosomiasis of bladder Vesical schistosomiasis bladder Schistosomiasis cystitis with bilharziasis	CD1D COLEC11 FCN2 MASP2 MBL2	10747 2220 4153 78989 912	Homo sapiens (human)
DOID:0110679	congenital myasthenic syndrome 4C Aliases: CMS Id CMS1D CMS4C FIM1 congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency congenital myasthenic syndrome type Id familial infantile myasthenia 1	GFPT1	2673	Homo sapiens (human)
DOID:1089	tethered spinal cord syndrome Aliases: spinal dysraphism	ABO ACHE ARSA CD38 CHKA COMT FOLR1 FOLR2 GPC5 HK1 ISYNA1 ITPK1 PCYT1A SLC2A2 SLC2A3 UGCG	1119 1312 2262 2348 2350 28 3098 3705 410 43 5130 51477 6514 6515 7357 952	Homo sapiens (human)
DOID:1700	X-linked ichthyosis Aliases: X-linked ichthyosis with steryl-sulphatase deficiency X-linked placental steryl-sulphatase deficiency X-linked recessive ichthyosis	ANXA5 ARSA CD44 CSPG4 DHCR7 FBP2 GLB1 HPGDS HPSE IDS LGALS1 MRC1 MTAP PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN RTN4R SMUG1 STS SUMF1	10855 142 1464 1717 23583 2720 27306 285362 308 3423 3956 410 412 4360 4507 5290 5291 5293 5294 5728 65078 8789 960	Homo sapiens (human)
DOID:7008	protoplasmic astrocytoma Aliases: Protoplasmic Astrocytic tumor	ACHE ACSL5 ADH1A ADH1B ADH1C ADH4 ADH6 AKR1A1 AKR1B1 AKR1C3 ALOX5 APRT ATRN B3GAT1 BDH2 BST2 CALR CAT CD248 CD44 CD55 CD74 CHI3L1 CHST15 CNTN2 CS CYP1B1 CYP4F3 ENPP1 EXT1 FCN2 FKTN G6PD GLB1 GOLPH3 HAS2 HJV HMMR HPGDS HPSE ICAM1 IDH1 IDH2 LGALS3 LGALS4 MMP25 MRC1 NEU1 PARP1 PFKFB3 PFKFB4 PGAM1 PGK1 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PLA2G10 PLA2G2A PLA2G4A PLB1 PLCB1 PLD1 PLD2 PRNP PRPS1 PTEN PTGDS PTGES PTGS2 RECK RTN4R SDC4 SDHA SGPL1 SLC2A3 SMUG1 SPHK2 ST8SIA2 ST8SIA4 STS TM7SF2 TNKS TYMP VCAM1 VCAN XYLT1	10327 10855 1116 124 125 126 127 130 142 1431 1462 148738 151056 1545 1604 1890 2131 2218 2220 231 23236 23583 240 2539 27087 2720 27306 3037 3161 3383 3417 3418 353 3958 3960 4051 412 43 4360 4758 51363 5167 51703 5209 5210 5223 5230 5290 5291 5293 5294 5310 5320 5321 5337 5338 5621 5631 56848 56898 57124 5728 5730 5743 6385 6389 64083 64131 64386 65078 6515 684 6900 7108 7412 7903 811 8128 8399 8434 8455 847 8644 8658 8879 9536 960 972	Homo sapiens (human)
DOID:13378	Kawasaki disease Aliases: Kawasaki's disease MLNS acute febrile MCLS acute febrile mucocutaneous lymph node syndrome mucocutaneous lymph node syndrome	ABO ACE ACHE ADIPOQ AMACR ATP6AP2 CAT CD14 CD177 CD209 CEACAM5 CERS6 CHI3L1 CLEC6A CLEC7A CYP2C9 CYP2E1 FCER2 FCGR3B FCN1 FUT1 GAPDH GLB1 HSD11B2 ICAM1 IL1R1 IL1RAP ITPKC KLRC1 KLRK1 LDHA MBL2 MDGA1 NCAM1 OLR1 PGK1 PLA2G7 PLCB1 PLCB4 PTGS2 SDC1 SELE SELP SLC35F5 ST6GAL1 STS TLR4 TNF ULBP1 VCAM1	10159 1048 1116 1559 1571 1636 2208 2215 2219 22914 23236 23600 2523 253782 2597 266727 2720 28 30835 3291 3383 3554 3556 3821 3939 412 4153 43 4684 4973 5230 5332 57126 5743 6382 6401 6403 64581 6480 7099 7124 7412 7941 80255 80271 80329 847 929 9370 93978	Homo sapiens (human)
DOID:3213	demyelinating disease Aliases: demyelinating disorder	ARSA CD1D FIG4 GALC GPC5 HPRT1 ICAM1 KL LGALS3 MAG PTGS2	2262 2581 3251 3383 3958 4099 410 5743 912 9365 9896	Homo sapiens (human)

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