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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 **4376 - 4400** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:8924	autoimmune thrombocytopenic purpura Aliases: Immune thrombocytopenic purpura idiopathic thrombocytopenic purpura primary thrombocytopenic purpura	ALB CD40 CD40LG CD86 FAS FCGR2A FCGR2B FCGR3A HLA-DQB1 HLA-DRB1 IL10 IL1A IL1RN IL2 IL4 ITGB3 PLAT TGFB1	213 2212 2213 2214 3119 3123 355 3552 3557 3558 3565 3586 3690 5327 7040 942 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:8927	learning disability Aliases: Academic skill disorder learning disorder	IL1RN	3557	Homo sapiens (human)	Alliance of Genome Resources
DOID:8929	atrophic gastritis Aliases: gastric atrophy	ATP4B HLA-DQB1 HLA-DRB1 PTPN11	3119 3123 496 5781	Homo sapiens (human)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	ANXA5 ATP7A ATP7B CP CYP27B1 HMGCR SMPD1	1356 1594 308 3156 538 540 6609	Homo sapiens (human)	Alliance of Genome Resources
DOID:8946	severe nonproliferative diabetic retinopathy Aliases: High risk non proliferative diabetic retinopathy Severe NPDR	PDGFRB	5159	Homo sapiens (human)	Alliance of Genome Resources
DOID:8947	diabetic retinopathy Aliases: Retinal abnormality - diabetes-related	ACE2 ACE ADIPOQ ADM ADRB3 AGER AGT AKR1B1 AKT1 ANGPT1 ANGPT2 AOC3 APOA4 APOB APOC3 APOE APOH AQP4 BDKRB1 BDNF CASP9 CAT CCL2 CCL5 CCN2 CD34 CD59 CDKAL1 CFB CFH CLDN1 CLU DLL4 EDN1 EGFR ELN ENG EP300 EPO F13A1 F3 F7 FLT1 FUCA1 GAPDH GC GGT1 GLO1 GLUL HFE HGF HIF1A HLA-B HLA-DQB1 HLA-DRB1 HRAS ICAM1 IGF1R IL10 IL1A IL6 INS INSR ITGA2 ITGA4 ITGAM ITGB3 KDM1A KEAP1 LTA MMP2 MMP9 NFE2L2 NGF NOS1 NOS3 NPPA NPR3 OCLN PDX1 PGF PIK3CG PON1 PPARGC1A PTEN RBP4 ROBO1 SERPINA4 SERPINE1 SERPINF1 SGF29 SLIT2 SOD1 SOD3 THBS1 TIMM44 TLR4 TNF VCAM1 VEGFA VPS26A VTN VWF WFS1 XRCC1	100506658 10469 10891 112869 1191 133 1490 155 1636 177 183 1906 1956 2006 2022 2033 2056 207 2152 2155 2162 23028 231 2321 2517 2597 2638 2678 2739 2752 284 285 3075 3077 3082 3091 3106 3119 3123 3265 337 338 3383 345 348 3480 350 3552 3569 3586 361 3630 3643 3651 3673 3676 3684 3690 4049 4313 4318 4780 4803 4842 4846 4878 4883 5054 5176 5228 5267 5294 5444 54567 54901 5728 59272 5950 6091 623 627 629 6347 6352 6647 6649 7057 7099 7124 7412 7422 7448 7450 7466 7515 842 847 8639 9076 9353 9370 947 9559 966 9817	Homo sapiens (human)	Alliance of Genome Resources
DOID:8955	sideroblastic anemia Aliases: ANEMIA SIDEROBLASTIC Anemia, hypochromic with iron loading	ABCB7 CALR TRNT1	22 51095 811	Homo sapiens (human)	Alliance of Genome Resources
DOID:896	metal metabolism disorder Aliases: inborn metal metabolism disorder	ATP7A ATP7B DTNBP1 TRPM6	140803 538 540 84062	Homo sapiens (human)	Alliance of Genome Resources
DOID:8970	subacute sclerosing panencephalitis Aliases: Immunosuppressive measles encephalitis Van Bogaert's sclerosing leukoencephalitis subacute sclerosing leukoencephalopathy	ACE IFNL1	1636 282618	Homo sapiens (human)	Alliance of Genome Resources
DOID:898	autosomal dominant polycystic kidney disease Aliases: ADPKD Congenital biliary ectasias POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1	ANGPT2 BICC1 C9 CD14 CFB EDN1 FLNC FOS GFER GPBAR1 IL1RN ITGA8 LATS1 LCN2 LRP2 LRP5 MMP1 MMP9 MTOR MYC NPHP3 PITX2 PKD1 PKD2 PKD2L1 PKD2L2 RPS6KB1 SERPING1 SLC34A1 SPP1 STAT6	151306 1906 2318 2353 2475 2671 27031 27039 285 3557 3934 4036 4041 4312 4318 4609 5308 5310 5311 6198 629 6569 6696 6778 710 735 80114 8516 9033 9113 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:8986	narcolepsy Aliases: Narcolepsy, without cataplexy paroxysmal sleep	CD40LG CHKB HCRTR2 HLA-DPB1 HLA-DQA1 HLA-DQB1 HLA-DRB1 MOG	1120 3062 3115 3117 3119 3123 4340 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:8991	cervix uteri carcinoma in situ Aliases: CIN III CIN III - carcinoma in situ of cervix CIN III - severe dyskaryosis Cervix Ca in situ Severe Dysplasia of the Cervix Uteri Severe dysplasia of cervix carcinoma in situ of cervix carcinoma in situ of uterine cervix carcinoma of cervix stage 0 cervical intraepithelial neoplasia grade III with severe dysplasia squamous intraepithelial neoplasia, grade III	ADAM9 BRCA1 CADM1 CD274 CD46 CDH1 CDKN1B CSF1R CTNNA1 DLG1 FASLG HDAC1 HDAC2 HDAC6 HLA-DRB1 IGFBP3 MLH1 MMP2 MSH2 PDCD1 PHB1 PTEN PTGS2 RB1 RELA SKP2 STAT3 TERT TLR9 TOP2A VEGFA XIAP	10013 1027 1436 1495 1739 23705 29126 3065 3066 3123 331 3486 356 4179 4292 4313 4436 5133 5245 54106 5728 5743 5925 5970 6502 672 6774 7015 7153 7422 8754 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:8997	polycythemia vera Aliases: Osler-Vaquez syndrome Polycythaemia rubra vera Proliferative polycythaemia chronic erythremia	CD36 ELANE EPOR HFE	1991 2057 3077 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:90	degenerative disc disease Aliases: cervical disc degenerative disease intervertebral disc degeneration lumbar disc degeneration vertebral disc disease	ACAN ADAMTS4 ADAMTS5 ASPN COL10A1 COL1A1 COL2A1 CRK FOS GSK3B MMP13 MMP1 MMP3 NGF NGFR PAPPA POSTN TIMP1	10631 11096 1277 1280 1300 1398 176 2353 2932 4312 4314 4322 4803 4804 5069 54829 7076 9507	Homo sapiens (human)	Alliance of Genome Resources
DOID:900	hepatopulmonary syndrome	CX3CL1 EDN1 EDNRB NOS3 TNF VEGFA	1906 1910 4846 6376 7124 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:9007	sudden infant death syndrome Aliases: Cot death Crib death SIDS Sudden death of nonspecific cause in infancy	SCN5A SLC6A4 VEGFA	6331 6532 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:9008	psoriatic arthritis Aliases: arthritis psoriatica arthropathic psoriasis	CCR2 CYP1A1 IL13 IL17A IRAK1 LTA MMP1 MMP3 PECAM1 STAT3 STAT4 TNF	1543 3596 3605 3654 4049 4312 4314 5175 6774 6775 7124 729230	Homo sapiens (human)	Alliance of Genome Resources
DOID:903	gastrointestinal lymphoma	KMT2D	8085	Homo sapiens (human)	Alliance of Genome Resources
DOID:905	Zellweger syndrome Aliases: cerebrohepatorenal syndrome congenital iron overload	ABCD3 IL2 PEX11B PEX19 PEX3 SCP2	3558 5824 5825 6342 8504 8799	Homo sapiens (human)	Alliance of Genome Resources
DOID:906	peroxisomal disease Aliases: peroxisomal disorder	ACBD5	91452	Homo sapiens (human)	Alliance of Genome Resources
DOID:9065	leishmaniasis	CCR5 IFNG IL4 SLC6A4	1234 3458 3565 6532	Homo sapiens (human)	Alliance of Genome Resources
DOID:9074	systemic lupus erythematosus Aliases: Lupus Erythematosus, systemic SLE - Lupus Erythematosus, systemic disseminated lupus erythematosus	ADAMTS13 AGER APOA1 C1QA C2 C3 C4A C4B C4B_2 CAST CCL2 CCR3 CCR5 CD40 CD40LG CD46 CD80 CFH CHAF1A CIITA CLU CR2 CTLA4 CXCR2 CYBB CYP1A1 DNASE1 DNMT1 ELN EP300 EPOR F2 FAS FCGR2A FCGR2B FCGR2C FCGR3A HLA-DQB1 HLA-DRB1 HSPA1A HSPA1L HSPD1 IFNG IKZF3 IL10 IL13 IL17A IL1RN IL21 IL21R IL23R IL2 IL5 INPP5D IRF5 JAK1 JUNB KLKB1 LBR LDLR LPA MAN2A1 MBL2 MKI67 MMP1 NOD2 P2RY12 PDCD1 PGF PLD4 PPARG PRDM1 PRF1 PTPRC RC3H1 RO60 SELL SFTPD SLC11A1 SNRNP70 SNRPC SNRPD1 SNRPD2 SOD2 STAT4 TAB2 TAB3 TAP1 TFPI THBD TIMD4 TLR5 TLR7 TLR9 TNF TNFRSF13B TNFRSF1A TNFRSF1B TRAF3IP2 VCAM1 VIM	100293534 10036 10758 11093 1191 122618 1232 1234 1380 149041 149233 1493 1536 1543 177 1773 1786 2006 2033 2057 2147 2212 2213 2214 22806 23118 23495 257397 3075 3119 3123 3303 3305 3329 335 3458 355 3557 3558 3567 3579 3586 3596 3605 3635 3663 3716 3726 3818 3930 3949 4018 4124 4153 4179 4261 4288 4312 50615 51284 5133 5228 54106 5468 5551 5788 59067 6347 639 6402 64127 6441 64805 6556 6625 6631 6632 6633 6648 6738 6775 6890 7035 7056 7100 712 7124 7132 7133 717 718 720 721 7412 7431 831 9103 91937 941 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:9111	cutaneous leishmaniasis Aliases: Asian Desert Cutaneous Leishmaniasis Leproid leishmaniasis diffuse cutaneous leishmaniasis	CAT CCR5 CD163 COL1A1 IL10 IL17A LTA MMP2 SLC11A1 SOD1 TLR2 TLR4 TLR9 TNF	1234 1277 3586 3605 4049 4313 54106 6556 6647 7097 7099 7124 847 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:9119	acute myeloid leukemia Aliases: AML - acute Myeloid Leukemia Leukemia, Myelocytic, acute acute myeloblastic leukaemia acute myeloblastic leukemia acute myelogenous leukaemia acute myelogenous leukemia acute myeloid leukaemia	ABCC3 ABCG2 ABL1 ACSL6 ASXL1 BMI1 BRD7 CALR CBL CCL2 CD86 CDH1 CDKN1B CFHR1 CHI3L1 CREBBP CSF2 CSF3 CSF3R CTLA4 CXCR4 CYP1A1 CYP2B6 DNMT1 EZH2 F3 FADD FAS FGFR1 FLT3 GATA2 GPI GPX1 HLA-DQB1 IDH1 IDH2 IL10 IL1A IL6 ITGAV ITGB3 KAT6A KIT KMT2A KRAS LPP MDM2 MEFV MLLT10 MYBL2 NCOA2 NF1 NOS3 NPM1 NRAS NSD1 NUP214 NUP98 PHF6 PICALM PLCB1 RUNX1 SAMHD1 SF3B1 SH3GL1 SOD2 SRSF4 TERT TET2 TFPI2 TFR2 TOP2A TOP2B TP53 TYMS VEGFA ZRSR2	1027 10499 1116 1387 1437 1440 1441 1493 1543 1555 171023 1786 2146 2152 2260 2322 23236 23305 23451 25 25939 2624 2821 2876 29117 3078 3119 3417 3418 355 3552 3569 3586 3685 3690 3815 3845 4026 4193 4210 4297 4605 4763 4846 4869 4893 4928 54790 6347 6429 64324 6455 648 6648 7015 7036 7153 7155 7157 7298 7422 7852 7980 7994 8021 8028 811 8233 8301 84295 861 867 8714 8772 942 9429 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:9120	amyloidosis Aliases: amyloid disease	ADIPOQ APCS CSF1 GOT1 SERPINE1 TNF TNFRSF1A TREM1 TTR	1435 2805 325 5054 54210 7124 7132 7276 9370	Homo sapiens (human)	Alliance of Genome Resources

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