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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 **5301 - 5325** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:0080600	COVID-19 Aliases: 2019 Novel Coronavirus (2019-nCoV) 2019-nCoV infection COVID19 SARS-CoV-2 infection Wuhan coronavirus infection Wuhan seafood market pneumonia virus infection	ABO ACE BDH1 IL1R1 LGALS3 SELE TNF	1636 28 3554 3958 622 6401 7124	Homo sapiens (human)
DOID:26	pancreas disease	ACE ALDH2 CEL CYP2E1 MSLN PLA2G2A PRPS1 PTEN	10232 1056 1571 1636 217 5320 5631 5728	Homo sapiens (human)
DOID:950	dacryoadenitis	ICAM1 LYZ	3383 4069	Homo sapiens (human)
DOID:8927	learning disability Aliases: Academic skill disorder learning disorder	ACAT1 ACER3 ACHE ACSL4 ADPRS AGA AGPAT2 AGRN ALDH3A2 ALDH5A1 ALDH7A1 ALDOB ALG11 ALG13 ALG14 ALG2 ALG9 ALOX12B AMT AMY1A AMY1B AMY1C ARSA ARSD ARSI ASAH1 ATP6AP2 ATP6V0A2 ATP6V1A B3GALNT2 B3GALT6 B3GLCT B4GALNT1 BCKDHA BCKDHB CA4 CACNA2D1 CALR CAT CD38 CERS1 CHAT CLN5 CMAS CNTN2 CNTN4 CNTN6 COG5 COG6 COG8 COLEC10 COLEC11 COMT CRPPA CTSA CYB5R3 CYP24A1 CYP27A1 CYP2U1 DAG1 DBT DCN DGCR2 DHCR24 DHCR7 DLD DPAGT1 EBP ENOSF1 EOGT EPM2A EXT1 EXT2 EXTL3 FASN FBP1 FCN2 FCSK FDFT1 FKRP FKTN FUCA1 FUT8 G6PC3 G6PD GAD1 GALT GAS1 GBA2 GBE1 GCK GCSH GGT1 GK GLB1 GLDC GLYCTK GMPPA GMPPB GNPAT GNPTAB GNS GPAA1 GPC3 GPC6 GPD2 GPI GUSB HACD1 HADH HADHA HADHB HEXA HGSNAT HK1 HMGCL HPRT1 HS6ST2 HSD17B12 IDH1 IDH2 IDH3A IDH3B IDS IDUA IL1RAP IL1RAPL1 IMPA1 INPP5E INPP5K KDSR KL L1CAM L2HGDH LARGE1 LDHA LDHD LFNG LSS MACROD2 MAG MAN1B1 MAN2B1 MAN2C1 MANBA MASP1 MBOAT7 MMUT NAGA NAGLU NANS NDST1 NEU1 NSDHL NTNG1 OCRL OGT PAFAH1B1 PAFAH1B3 PAPSS2 PARP1 PC PCCA PCCB PCYT1A PDHA1 PDHX PDIA3 PGAP1 PGAP2 PGAP3 PGK1 PGM3 PIGA PIGB PIGC PIGG PIGL PIGN PIGO PIGP PIGQ PIGU PIGV PIGW PIK3CA PIK3CB PIK3CD PIK3CG PLCH2 PMM2 PNP PNPLA6 POMGNT1 POMGNT2 POMK POMT1 POMT2 PPT1 PRPS1 PTDSS1 PTEN RENBP RXYLT1 SC5D SDHA SDHB SDHC SDHD SGSH SLC17A5 SLC2A10 SLC33A1 SLC35A1 SLC35A2 SLC35A3 SLC39A8 SMC3 SRD5A3 ST3GAL3 ST3GAL5 STS STT3B SUCLG1 SULT1E1 SUMF1 SYNJ1 TECR TKT TMTC3 TNFRSF10C TPI1 TUSC3 TYMP UGCG UMPS XYLT1 XYLT2	10082 10159 10329 10466 10555 10559 10584 10585 10682 10715 10908 1103 11141 11253 113612 1203 126792 128869 1312 132158 138050 140733 142 145173 148789 152330 1591 1593 160418 1605 1629 1634 1717 1718 1727 1738 175 1798 1890 197257 197258 199857 201595 2131 2132 2137 2182 2194 2203 2218 2220 2222 224 22854 229 23443 23545 23556 242 2517 2530 2531 2539 2571 2583 2592 2619 2632 2645 26503 2653 2678 2710 2719 2720 27255 2731 27315 275 276 277 278 2799 2820 2821 284098 285203 285362 2923 2990 29925 29926 29954 3030 3032 3033 3073 3098 3155 3251 3340 340075 3417 3418 3419 3420 3423 3425 3556 3612 375790 38 3897 3939 3955 4047 4099 410 412 4123 4125 4126 414 427 43 440138 4594 4668 4669 4758 4860 4952 501 5048 5050 50814 5091 5095 5096 51144 51227 5130 5160 51763 523 5230 5238 5277 5279 5290 5291 5293 5294 5373 54187 5476 54872 54936 55331 5538 55556 55624 55650 55907 5631 5648 56623 5728 57511 57704 593 594 5973 6309 6389 6390 6391 6392 64116 64131 64132 6448 6487 6783 6900 7086 7167 729920 7355 7357 7372 762 781 78989 79143 79147 7915 79158 7957 79644 79796 79868 7991 79944 80055 8050 81031 811 84197 84342 8443 847 84720 8473 84892 85365 8733 8794 8802 8867 8869 90161 9060 9091 9126 9197 9200 9215 92579 93210 9365 9487 9488 952 9524 9651 9791 9993	Homo sapiens (human)
DOID:3081	cystic lymphangioma Aliases: cystic Hygroma	LPL PIK3CA SLC26A2 TGDS	1836 23483 4023 5290	Homo sapiens (human)
DOID:0110716	Warburg micro syndrome 1 Aliases: Micro Syndrome 1 WARBM1	AKR1C4 CNTN3 COG1 CYP2B6 DGCR2 FREM1 G6PD GAS1 GYS2 LSS NT5E SLC26A2	1109 1555 158326 1836 2539 2619 2998 4047 4907 5067 9382 9993	Homo sapiens (human)
DOID:0060782	EEC syndrome Aliases: Rudiger syndrome 1 Walker-Clodius syndrome ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome ectrodactyly-ectodermal dysplasia-clefting syndrome	ENO1 LCT MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN	2023 3938 4360 5290 5291 5293 5294 5728	Homo sapiens (human)
DOID:0080548	Noonan syndrome with multiple lentigines 1 Aliases: LEOPARD syndrome 1	PIK3CA PIK3CB PIK3CD PIK3CG PTEN	5290 5291 5293 5294 5728	Homo sapiens (human)
DOID:0050572	cone-rod dystrophy Aliases: cone-rod retinal dystrophy	ABO ACE ACOX1 ADH7 ALDH3A2 ALDH7A1 ALG12 ALOX12 AMACR ARSI CA4 CACNA2D4 CANX CD38 CD44 CD48 CD74 CNTN3 CNTN6 COG4 CTNS CYP19A1 DGKE DHDDS ECHS1 ELOVL4 ELOVL6 FASN FKRP G6PD GAL3ST1 GK GLO1 GMPPB GNPTG H6PD HADH HADHA HADHB HGSNAT HK1 HK2 HKDC1 HSD11B1 HSD17B6 IDH2 IDH3A IDH3B IMPA1 KL LARGE1 LGALS1 LPCAT1 MDH1 NAGLU NGLY1 NYX PDHA1 PIK3CA PIK3CB PIK3CD PIK3CG PMM2 PNPLA2 PNPLA6 POMGNT1 POMT1 POMT2 PRNP PTEN RGMA RPE SDHA SDHB SDHD SFTPD SGSH SIGLEC7 SLC35A1 SMC3 SOAT1 SYNJ1 TMED3	10559 10585 10908 131 138050 1497 1588 1636 1892 2194 224 23423 23600 239 2539 25839 27036 2710 27255 2739 28 29925 29954 3030 3032 3033 3098 3099 3290 340075 3418 3419 3420 3612 3956 4190 4669 501 5067 51 5160 5290 5291 5293 5294 5373 55624 55768 5621 56963 57104 5728 60506 6120 6389 6390 6392 6441 6448 6646 6785 762 79071 79087 79147 79888 79947 80201 821 84572 8526 8630 8867 9126 9215 93589 9365 9514 952 9563 960 962 972	Homo sapiens (human)
DOID:4015	sarcomatoid carcinoma Aliases: spindle cell carcinoma	ABO ACACA ACACB ACE ACSL1 ACSL5 ACSM1 AGXT AKR1B10 AKR1B1 AKR1C3 ALDH2 ALDH3A1 ALDH7A1 ALDOA ALOX15 ALOX15B ALOX5 ALPI ALPP AMACR ANXA4 ANXA5 APRT ARSA ASAH1 B3GAT1 B4GALNT2 BAAT C1GALT1 CACNA2D3 CALR CAT CBR1 CD109 CD14 CD1D CD248 CD38 CD44 CD55 CD74 CDH13 CDS1 CEACAM5 CEACAM6 CEACAM7 CERS2 CHGA CHPT1 CPT1A CPT2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP24A1 CYP27B1 CYP2E1 CYP3A5 CYP3A7 CYP4F3 DAG1 DCN DCXR DHCR24 DHDH EFNA1 ENO1 ENO2 ENPP1 FASN FBP1 FCGR3B FH FOLR1 FUT1 FUT3 FUT4 FUT6 G6PC1 GALNT3 GALNT6 GAPDH GCNT1 GGT1 GLB1 GLO1 GLUL GOLPH3 GPC3 GPLD1 GPX2 GPX3 GUSB HAGH HAS1 HAS2 HAS3 HK2 HMGCS2 HMMR HPGDS HPSE HSD17B12 HSD3B1 HSPG2 HYAL1 HYAL2 HYAL3 ICAM1 IDH1 IDH2 INPP4B ITLN1 L1CAM LDHA LDHB LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LMAN1 LPIN1 LPL LY6K LYPD5 LYPLA1 MAN2C1 MBD4 MCAT MDH2 MELTF MGAT5 MICA MINPP1 MMP25 MPG MRC1 MSLN MTAP MUTYH NAMPT NCAM1 NEIL1 NEU1 NEU3 NT5E NTHL1 OGG1 OPCML PARP1 PDHA1 PDIA3 PFKM PGAM1 PGK1 PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G1B PLA2G2A PLA2G6 PLAUR PLCD1 PLCE1 PLCG1 PLD1 PLD2 PLPP2 PNP PPP1R3A PRKAA2 PRNP PRPS1 PTEN PTGDS PTGES3 PTGES PTGS1 PTGS2 PYGM QTRT1 RECK SCD SDC1 SELE SFTPC SHMT1 SIGLEC12 SIGLEC9 SIRT2 SIRT6 SLC2A2 SLC35A2 SMC3 SMUG1 SPHK1 SPHK2 SRGN ST3GAL4 ST3GAL6 ST6GAL1 ST8SIA4 STS TKT TKTL1 TM7SF2 TNKS TYMP UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B7 UMPS VCAN VTCN1	100507436 1012 10135 10232 1040 10402 10434 1048 10728 10825 10855 1087 1113 11226 116285 124872 128869 135228 1374 1376 142 1462 1543 1544 1545 1551 1571 1577 1586 1588 1591 1594 1604 1605 1634 1636 1718 189 1890 1942 2023 2026 217 218 2180 2194 2203 2215 226 2271 22933 231 23175 2348 23583 23600 240 246 247 248 250 2523 2525 2526 2528 2538 2591 2597 2650 2678 27087 27180 2719 2720 27294 27306 27349 2739 2752 28 2822 284348 2877 2878 2923 2990 29956 3029 3036 3037 3038 307 308 3099 31 3158 3161 32 3283 3339 3373 3383 3417 3418 353 3897 3939 3945 3956 3958 3960 3964 3965 3998 4023 4051 410 412 4123 4191 4241 4249 427 4350 4360 4507 4595 4680 4684 4758 4860 4907 4913 4968 4978 501 51144 51181 51196 51548 5160 5167 51703 5213 5223 5230 5289 5290 5291 5293 5294 5315 5319 5320 5329 5333 5335 5337 5338 54575 54576 54577 54578 54579 54600 54657 54658 54659 54742 5506 5552 55600 5563 55799 5621 5631 56848 56886 56913 56994 570 57016 57124 5728 5730 5742 5743 5837 6319 6382 6401 64083 64386 6440 6470 6480 6484 6514 7086 7108 7355 7364 7372 7903 79661 79679 811 81890 8277 8372 8398 8434 847 8612 8644 8658 8692 873 8821 8877 8930 89858 912 9126 929 952 9536 9562 960 972	Homo sapiens (human)
DOID:2843	long QT syndrome Aliases: LQT long Q-T syndrome	ACADM ACSBG1 ALG10 ALG10B CNTN3 CYP1A1 KCNQ1 PTEN SCD SLC2A5 SQLE	144245 1543 23205 34 3784 5067 5728 6319 6518 6713 84920	Homo sapiens (human)
DOID:0081223	glycosylphosphatidylinositol biosynthesis defect 16 Aliases: Intellectual developmental disorder, autosomal recessive 62	PIGC	5279	Homo sapiens (human)
DOID:3320	Tay-Sachs disease Aliases: GM2 gangliosidosis, type 1 hexosaminidase A deficiency	ARSA GBA1 GM2A HEXA HEXB HEXD NEU3 OGA	10724 10825 2629 2760 284004 3073 3074 410	Homo sapiens (human)
DOID:11759	hypochromic anemia Aliases: ANEMIA HYPOCHROMIC	ACO1 CACNA2D3 CAT CD55 GOLPH3 IDUA LALBA PLA2G4A PLA2G6	1604 3425 3906 48 5321 55799 64083 8398 847	Homo sapiens (human)
DOID:2012	Nezelof syndrome Aliases: Nezelof's syndrome T-cell immunodeficiency with thymic aplasia TIDTA thymic aplasia thymic dysplasia with normal immunoglobulins	DGCR2 IL18R1 PNP	4860 8809 9993	Homo sapiens (human)
DOID:0110443	dilated cardiomyopathy 1B	ACADVL ACE BDH1 CHKB CNTN3 CPT2 DAG1 DOLK FASN FKRP FKTN GLB1 GPX1 HACD1 HADH HADHA HADHB HJV HMGCL HPRT1 LDHA LGALS3 LPL MDH1 MICA MTM1 NAMPT NCAM1 NDUFAB1 PCYT1A PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 POMT2 RENBP SDHA SDHD SLC2A10 SLC2A4	100507436 10135 1120 1376 148738 1605 1636 2194 2218 22845 2720 2876 29954 3030 3032 3033 3155 3251 37 3939 3958 4023 4190 4534 4684 4706 5067 5130 5236 5290 5291 5293 5294 5973 622 6389 6392 6517 79147 7941 81031 9200	Homo sapiens (human)
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	ABO ACACA ACAN ACE ACHE ACOT4 ACOT7 ACOX1 ACSM3 ACSS2 ACYP2 ADH1B ADH1C ADPRS AGXT AKR1A1 AKR1B1 ALDH2 ALDH7A1 ALG1 ALOX12 ALOX5 AMACR APRT ARSA ATP6AP2 BCKDHA CALR CAT CD14 CD38 CD44 CD74 CDH13 CEACAM5 CEACAM7 CHAT CHI3L1 CHIT1 CLEC16A CLEC1B COMT CSPG4 CYP11B1 CYP11B2 CYP19A1 CYP1A1 CYP24A1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2J2 CYP2R1 CYP3A4 CYP3A5 CYP46A1 CYP4A11 CYP4F2 DCN DHCR24 DLD EBP EFNA5 ENO1 ENO2 ENPP1 ENPP2 EPHX2 FADS1 FADS2 FCGR3B FCN1 FCN2 FUT1 G6PD GAL3ST1 GALNT2 GALNT3 GBE1 GFRA1 GGT1 GLA GLCE GLO1 GLUL GPI GPX1 GPX3 HACD1 HADHA HJV HK2 HPGDS HPSE2 HPSE HSD11B2 HSPG2 ICAM1 IDS IL18R1 IL18RAP IL1R1 IL1RL1 IMPA1 IMPA2 INPP5D INPP5K INPPL1 ISYNA1 ITPK1 KL LCAT LDHC LGALS1 LGALS2 LGALS3 LGALS9 LIPC LPL LTA4H LTC4S MAG MAN2B2 MASP1 MASP2 MBL2 ME1 MGLL MMUT MRC1 MTAP NAAA NAMPT NANS NCAM1 NDUFAB1 NEIL1 NT5E NTNG1 OGG1 OLR1 PARP1 PC PCYT1A PFKFB3 PIK3C2B PIK3CA PIK3CB PIK3CD PIK3CG PKD1L3 PKM PLA2G15 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLCG1 PLPP3 PRG3 PRKAA2 PRNP PRSS21 PTEN PTGES PTGIS PTGS1 PTGS2 QTRT1 RENBP RGMB RTN4R SACM1L SCD SDC1 SDC4 SELE SELL SELP SEMA7A SFTPA1 SFTPD SHMT1 SIGLEC7 SIRT2 SIRT6 SLC17A5 SLC2A10 SLC33A1 SLC35A1 SLC39A8 SLC5A1 SMPD1 SMUG1 SOAT1 SPHK2 ST3GAL4 ST8SIA4 STS SULT1E1 TBXAS1 TIGAR TM7SF2 TMED9 TNKS UGCG UGT1A1 UGT2B4 UMOD UNG VCAM1 VCAN XYLB XYLT1 XYLT2	1012 10135 10159 10327 10394 1048 10559 10682 10747 10855 10858 1087 10942 1103 1116 1118 11332 11343 120227 122970 125 126 1312 142 1462 1464 148738 1543 1555 1557 1558 1559 1571 1573 1576 1577 1579 1584 1585 1588 1591 1634 1636 1718 1738 176 189 1946 2023 2026 2053 217 2215 2219 2220 22854 22908 22933 231 23274 23324 23583 23600 23659 239 240 2523 2539 2590 2591 26035 2632 26503 2674 2678 27036 27163 2717 27306 2739 2752 28 2821 285704 2876 2878 3030 3099 31 3291 3339 3383 3423 342372 353 3554 3612 3613 3635 3636 3705 3931 3948 3956 3957 3958 3965 3990 3992 4023 4048 4056 4099 410 412 4153 4199 43 4360 4507 4594 4684 4706 4907 4968 4973 501 5091 51 51266 5130 51477 51548 5167 5168 51763 5209 5287 5290 5291 5293 5294 5315 5319 5320 5321 5335 54187 54658 54732 54936 5563 55902 56052 5621 5648 56848 57103 5728 5740 5742 5743 593 5973 60495 6296 6319 6382 6385 6401 6402 6403 64116 64131 64132 6441 6470 6484 65078 6523 653509 6609 6646 6783 6916 7108 7357 7363 7369 7374 7412 7903 7941 79661 81031 811 81890 8398 847 8482 8529 8613 8658 8807 8809 9173 9197 9200 929 9365 9415 9514 952 9536 960 972 98 9942	Homo sapiens (human)
DOID:5667	sweat gland carcinoma Aliases: carcinoma of the Sweat gland	CEACAM5 SMUG1	1048 23583	Homo sapiens (human)
DOID:0070146	hereditary sensory neuropathy type 4 Aliases: hereditary sensory neuropathy type IV insensitivity to pain, congenital, with anhidrosis	PKLR SPTLC1	10558 5313	Homo sapiens (human)
DOID:1307	dementia	ACE ACHE ACOT7 ADH1C ADIPOQ AGPS AKR1C4 ALDH2 ARSA ASAH1 ASAH2 ATP6V0A2 ATP6V1A CD38 CEACAM5 CEACAM7 CERS1 CHAT CHI3L1 CHIT1 COMT CSPG4 CYP19A1 CYP27A1 DHDDS DLD EBP EPHX2 EPM2A G6PD GBA1 GBA2 GBE1 GM2A GNE GPX1 H6PD HEXA HPGDS HSD11B1 ICAM1 IDH1 INPP5D INPP5K KL LIPG LPL NAGLU NDUFAB1 PAFAH1B1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 PLAUR PLD1 PNPLA6 PRNP PSAP PTGS2 SCD SDHA SDHB SDHD SFTPC SIRT2 SLC17A5 SLC2A3 SLC33A1 SMUG1 SORD SPTLC1 ST3GAL4 SUCLA2 SYNJ1 TGDS TIGAR TPI1 UGCG VCAM1	10020 1048 10558 10682 10715 1087 10908 1103 1109 1116 1118 11332 126 1312 1464 1588 1593 1636 1738 2053 217 22933 23483 23545 23583 2539 2629 2632 26503 27306 2760 2876 3073 3290 3383 3417 3635 4023 410 427 43 4669 4706 5048 51763 523 5290 5291 5293 5294 5329 5337 5621 5660 56624 57103 5743 57704 6319 6389 6390 6392 6440 6484 6515 6652 7167 7357 7412 7941 7957 79947 8540 8803 8867 9197 9365 9370 9388 952 9563	Homo sapiens (human)
DOID:0060602	alpha-methylacyl-CoA racemase deficiency Aliases: AMACR deficiency	AMACR HSD17B4	23600 3295	Homo sapiens (human)
DOID:0111049	platelet-type bleeding disorder 17 Aliases: BDPLT17 hereditary thrombasthenia-thrombocytopenia	DLD GOLPH3 HPSE2 HPSE LGALS1 LGALS8 NAAA NAGLU PLA2G1B PLA2G2A PLA2G6 SELP VCAM1	10855 1738 27163 3956 3964 4669 5319 5320 60495 6403 64083 7412 8398	Homo sapiens (human)
DOID:14695	galactokinase deficiency Aliases: Galactosemia II	AKR1B1 ALG9 CYP51A1 G6PD GALE GALK1 GALM GALT GK GP2 LGALS1 MGAT1 SLC2A2 UGP2 UGT8	130589 1595 231 2539 2582 2584 2592 2710 2813 3956 4245 6514 7360 7368 79796	Homo sapiens (human)
DOID:0090039	torsion dystonia 6	ALDH5A1	7915	Homo sapiens (human)
DOID:2228	thrombocytosis Aliases: Thrombocythaemia	ACAT1 CALR CD177 HMGCL NAAA PMM2	27163 3155 38 5373 57126 811	Homo sapiens (human)

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