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GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1376 - 1400** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:13088	periventricular leukomalacia	MBP TNF	4155 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:13078	eumycotic mycetoma Aliases: Madura foot Maduromycosis, mycotic Mycotic mycetoma eumycetoma maduromycosis	COMT	1312	Homo sapiens (human)	Alliance of Genome Resources
DOID:1307	dementia	ADIPOQ BACE1 BAX BCHE CAPZB DRD2 E2F1 EGFR GRN HMGCR IGF1R LRP8 LRPAP1 MAPT NGFR NOS2 NOTCH4 NRG1 PCSK1N PLA2G7 PON1 VCP VLDLR	1813 1869 1956 23621 27344 2896 3084 3156 3480 4043 4137 4804 4843 4855 5444 581 590 7415 7436 7804 7941 832 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:13042	persistent fetal circulation syndrome Aliases: Fetal circulation Persistent fetal circulation Persistent foetal circulation congenital alveolar capillary dysplasia with misalignment of pulmonary veins persistent foetal circulation syndrome persistent pulmonary hypertension of the newborn	CPS1 ITGAM NOS3 PTEN	1373 3684 4846 5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:13025	retinopathy of prematurity Aliases: Retrolental fibroplasia premature retinopathy	ANGPT2 DLL4 EPO EPOR FLT1 HGF HLA-B HLA-DRB1 ICAM1 IGFBP3 IHH IL10 KDR NOS1 NOS2 NOS3 NOTCH1 SERPINE1 SERPINF1 SOD1 VEGFA	2056 2057 2321 285 3082 3106 3123 3383 3486 3549 3586 3791 4842 4843 4846 4851 5054 5176 54567 6647 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:13001	carotid stenosis Aliases: Carotid artery stenosis Stenosis, carotid artery	F2 IL10 IL4 LPA MMP1 MMP3 MT2A NR1H3 PLA2G7 PROCR PTGIS TLR2 TLR4 VCAM1	10062 10544 2147 3565 3586 4018 4312 4314 4502 5740 7097 7099 7412 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:12995	conduct disorder	AR DRD4 HTR1B	1815 3351 367	Homo sapiens (human)	Alliance of Genome Resources
DOID:12987	agranulocytosis Aliases: Granulocytopenic disorder Granulopenia granulocytopenia	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:12986	leukostasis	ACE SERPINF1	1636 5176	Homo sapiens (human)	Alliance of Genome Resources
DOID:12978	Plasmodium vivax malaria Aliases: Malaria by Plasmodium vivax Vivax Malaria	ACKR1	2532	Homo sapiens (human)	Alliance of Genome Resources
DOID:12971	hereditary spherocytosis Aliases: Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia	ANK1 EPB42 SLC4A1 SPTA1 SPTB	2038 286 6521 6708 6710	Homo sapiens (human)	Alliance of Genome Resources
DOID:12960	acrocephalosyndactylia Aliases: Apert syndrome	FGFR1 FGFR2 TWIST1	2260 2263 7291	Homo sapiens (human)	Alliance of Genome Resources
DOID:12935	alcoholic cardiomyopathy Aliases: Alcohol-induced heart muscle disease Dilated cardiomyopathy secondary to alcohol	NOS1 PPARG	4842 5468	Homo sapiens (human)	Alliance of Genome Resources
DOID:12934	Kearns-Sayre syndrome	TFAM	7019	Homo sapiens (human)	Alliance of Genome Resources
DOID:12932	endomyocardial fibrosis Aliases: African endomyocardial fibrosis Becker's disease Endomyocardial sclerosis obscure African cardiomyopathy	ACE CCL2 CCN2 UTS2R	1490 1636 2837 6347	Homo sapiens (human)	Alliance of Genome Resources
DOID:12930	dilated cardiomyopathy Aliases: primary dilated cardiomyopathy	ABCC9 ACE ACTC1 ADRB1 ADRB2 AGT AGTR1 AGTR2 APOE BAG3 BAX CACNG8 CAP2 CASP9 CAT CD40 CDK8 CENPF COL15A1 COL18A1 CS CTSL CTSV CXCR3 CYP1A1 CYP2C19 DAG1 DES DICER1 DLL1 DLL4 DMD DNER DNM1L DSC2 DSG2 DSP DYRK1A ECE1 EDN1 EEF1A1 EEF1A2 EGFR EMD ERBB2 EYA4 FADS2 FAS FKRP FLNC GDF1 GPX1 HFE HLA-DQB1 HP ICAM1 ICAM3 ICAM4 IL10 IL13RA2 IRF4 ITPR1 JAG1 JAG2 LDB3 LEPR LMNA LMOD2 LTBP2 MAP3K7 MAS1 MBNL1 MBNL2 MED1 MEF2A MMP14 MMP1 MMP2 MRGPRD MYH15 MYH1 MYH7 NCOA6 NEBL NFATC4 NOS2 NPPA NPPB NR2F2 OBSCN ORAI1 ORAI3 PDCD1 PDLIM5 PHC1 PPARGC1A PPP3CA PRKCA PTGER4 PTPN11 RAB1A RANBP1 RBM20 RBM24 RBP4 RBPJ RPS6KB1 RTF1 RTTN SNAI1 SOD2 SP4 SRF STIM1 STIM2 TIMP3 TNF TNNI3 TP53 TRDN TTN VCL VEZF1 YME1L1	10059 10060 10150 1024 10345 10486 10529 10611 1063 10730 10891 11155 116512 1306 1431 1514 1515 153 154 1543 1557 1605 1636 1674 1756 182 1824 1829 183 1832 185 1859 186 1889 1906 1911 1915 1917 1956 2010 2064 2070 221662 22989 23054 23168 2318 23405 25914 2657 282996 2833 28514 2876 3077 3119 3240 3383 3385 3386 348 3516 355 3586 3598 3662 3708 3714 3953 4000 4053 4142 4154 4205 4312 4313 4323 442721 4619 4625 4776 4843 4878 4879 5133 54567 5469 5530 5578 5734 57620 5781 581 5861 5902 59283 5950 6198 6615 6648 6671 6722 6786 6885 70 7026 7078 7124 7137 7157 7273 7414 7716 79147 80781 84033 842 847 84876 92737 93129 9415 9531 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:12918	thromboangiitis obliterans Aliases: Buerger's disease Presenile gangrene	AGER CRHR1 ELN HLA-A HLA-DRB1 LINC02210-CRHR1 VCAM1	104909134 1394 177 2006 3105 3123 7412	Homo sapiens (human)	Alliance of Genome Resources
DOID:12897	submandibular gland disease	FN1	2335	Homo sapiens (human)	Alliance of Genome Resources
DOID:12895	keratoconjunctivitis sicca Aliases: KCS	CCR5 IL6 TNF	1234 3569 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:12894	Sjogren's syndrome Aliases: Sicca syndrome Sjogren syndrome xerodermosteosis	APOE BDNF BST2 CAST CCR5 CCR7 CD40LG CTLA4 CYP19A1 CYP1A1 E2F1 FAS GDNF HLA-DQA1 HLA-DQB1 HLA-DRB1 HNRNPH1 ICAM1 IFNG IL10 IL13 IL1RN IL23R IL2 IL2RA IL4 IL6 LTA MMP3 MMP9 MUC16 MUC19 MUC5AC NEFL PON1 REG1A SATB1 SELP ST14 STAT4 TGFB1 THBS1 TNF TNFSF13B TRAF3IP2 VIM	10673 10758 1234 1236 149233 1493 1543 1588 1869 2668 283463 3117 3119 3123 3187 3383 3458 348 355 3557 3558 3559 3565 3569 3586 3596 4049 4314 4318 4586 4747 5444 5967 627 6304 6403 6768 6775 684 7040 7057 7124 7431 831 94025 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:1289	neurodegenerative disease Aliases: degenerative disease	ACO2 AIMP1 APLP2 BCL11A BCL11B CAT CLEC16A DEGS1 DEGS2 DVL1 DVL3 DYNC1H1 EPO FAT4 FIG4 FUS GC GGA2 GGA3 GRIA1 GRIA2 GRIA3 GRIA4 GRIK1 GRIK2 GRIK3 GRIN1 HNRNPA1 HNRNPA1L2 HNRNPA2B1 HNRNPA3 HPDL HTT KIF5B LATS1 LATS2 LRRK2 MAPT MARK2 MARK3 MARS2 MEGF10 MEGF11 MTMR10 MTMR11 NFKB1 NFKB2 NPLOC4 NRDC NUP50 PACSIN2 PEAR1 PLA2G6 PNPLA6 PNPLA7 PON1 PON2 PON3 PRKAG2 PRKAG3 PSMA3 PSMA5 PSMB1 PSMC4 PSMD2 PTCH1 PTCH2 RASA1 RHOA RHOB RHOC SARM1 SCNN1A SCNN1B SCNN1D SCNN1G SDHA SLC17A6 SLC17A8 SLC1A1 SLC1A2 SLC1A3 SLC1A4 SLC1A5 SLC1A6 SLC1A7 STK4 TARDBP TBP TPI1 TRAK1 TRAK2 TRPC4 TRPC5 TSPAN3 TSPAN7 UBQLN1 UBQLN2 UBQLN4 UBR1 UFD1 VAPA VAPB VCP YAP1 YBX2	10099 10413 10762 10903 10908 11252 120892 123099 144983 1778 1855 1857 197131 2011 2056 220988 22906 23062 23098 23163 23274 23435 246213 2521 2638 26524 2890 2891 2892 2893 2897 2898 2899 2902 29978 29979 3064 3178 3181 334 375033 375775 3799 387 388 389 4137 4140 4790 4791 4898 50 51087 51422 53335 53632 5444 5445 5446 54893 55666 5684 5686 5689 56893 5704 5708 57084 5727 5921 6337 6338 6339 6340 6389 64919 6505 6506 6507 6509 6510 6511 6512 66008 6789 6908 7102 7167 7223 7224 7353 7415 79633 8398 84465 84466 847 84842 8560 8643 9113 9217 9218 9255 92935 9896	Homo sapiens (human)	Alliance of Genome Resources
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	ADIPOQ AGER AGT APOA4 APOB CCL2 CD40LG CFH DBI ENPP1 FGB FTO GHRL GIPR GPX1 GPX3 GYS1 HP HSPA1A LIPG MPO PLAUR PPARG PPARGC1A PTGS2 TLR9 UBR1	10891 1622 177 183 197131 2244 2696 2876 2878 2997 3075 3240 3303 337 338 4353 5167 51738 5329 54106 5468 5743 6347 79068 9370 9388 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:12859	choreatic disease Aliases: chorea hereditary chorea	HLA-DQA1 HLA-DQB1 HLA-DRB1 NKX2-1 VPS13A	23230 3117 3119 3123 7080	Homo sapiens (human)	Alliance of Genome Resources
DOID:12858	Huntington's disease Aliases: HD Huntington disease Huntington's chorea	ABAT ACHE AGTR1 APOA4 ATF2 BAX BCHE BDNF CASP9 CAT CNR2 CREB1 CREBBP CTSH DNAJB2 DRD1 E2F1 EIF2AK2 ELK1 F2 FAS FASLG FKBP11 FOXP1 GIT1 GLUL GPX1 GPX6 GRIK2 GRIN2A GRIN2B HSF1 HTT IL6 IL6R ITPR1 LCP1 LEP MAP2 MBP MMP9 MTNR1A NCOR1 ND3 NFE2L2 NGFR NOG NOS3 NPY2R NRF1 OPTN PACSIN2 PARP1 PLS1 PLS3 PPARD PPARGC1A PPP1R9A PRKAA1 PTGS2 QPRT RRS1 SETDB1 SIN3A SIRT1 SLC18A3 SLC1A2 SRSF6 SYNE3 TBP TFAM TRIP10 UCP2 WIPI1 WIPI2 YBX2 ZDHHC13	10133 10891 11252 1269 1385 1386 1387 142 1512 161176 18 1812 185 1869 2002 2147 23212 23411 23475 257202 25942 26100 27086 2752 2876 28964 2898 2903 2904 3064 3297 3300 337 355 356 3569 3570 3708 3936 3952 4133 4155 43 4318 4537 4543 4780 4804 4846 4887 4899 51087 51303 5357 5358 54503 5467 55062 55607 5562 5610 5743 581 590 627 6431 6506 6572 6908 7019 7351 842 847 9241 9322 9611 9869	Homo sapiens (human)	Alliance of Genome Resources
DOID:12849	autistic disorder Aliases: Kanner's syndrome autism autistic disorder of childhood onset childhood autism infantile autism	ANK2 C4B CCL2 CNTNAP2 DAB1 EIF4E EN2 FOXP2 GABRA2 GABRA4 GABRA5 GABRB1 GABRB2 GABRR2 GLO1 GRM8 GRN HLA-DRB1 HRAS HSPD1 IL6 KCNQ3 KDM4C KMT2E LAMB1 MECP2 MET MTR NF1 NLGN1 NLGN3 NLGN4X NTRK2 PECAM1 PIK3CG PTCHD1 RELN RPP25 SETDB1 SHANK2 SLC25A12 SLC6A4 SLC9A9 TNF VLDLR	139411 1600 1977 2020 22871 22941 23081 2555 2557 2558 2560 2561 2570 26047 2739 285195 287 2896 2918 3123 3265 3329 3569 3786 3912 4204 4233 4548 4763 4915 5175 5294 54413 54913 55904 5649 57502 6347 6532 7124 721 7436 8604 93986 9869	Homo sapiens (human)	Alliance of Genome Resources

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