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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 **1301 - 1325** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	ABO ACACA ACACB ACADS ACAN ACAT1 ACAT2 ACE ACHE ACLY ACOT2 ACOT7 ACSL1 ACSS2 ADH1A ADH1B ADH1C ADH5 ADIPOQ ADRB3 AGPAT2 AGXT AKR1A1 AKR1B10 AKR1B1 ALDH1B1 ALDH2 ALDH6A1 ALDOA ALOX12 ALOX15 ALOX15B ALOX5 ALPL ANXA5 APRT ARSA ARSB ARSD ARSI ASGR1 ATP6AP2 ATP6V0A2 B3GAT1 B4GALNT1 B4GALNT2 B4GALT1 CACNA2D2 CALR CANX CAT CD14 CD1D CD248 CD44 CD74 CD93 CDH13 CEL CERS1 CFC1 CH25H CHGA CHI3L1 CHIT1 CHST3 CHST9 CLEC10A CLEC1B CLEC6A CLEC7A CLEC9A CNTN3 COG2 COG5 COG6 COMT CPT1A CPT2 CS CYP11B2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP21A2 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2J2 CYP2R1 CYP3A4 CYP3A5 CYP4A11 CYP4F2 CYP7A1 DAG1 DCN DGAT1 DGKK DHCR24 DHCR7 DLAT DLD DPEP2 DPEP3 EBP EFNA5 ELOVL2 ELOVL6 ENPP1 ENPP7 EPHX2 EXTL3 FADS1 FADS2 FCGR3B FCN1 FCN2 FCN3 FDPS FMOD FOLR2 FUT3 FUT8 G6PD GAD1 GAL3ST1 GALNT2 GALNT3 GALNT4 GALNT7 GAPDH GCK GGT1 GK GLO1 GLT1D1 GLUL GPD1L GPI GPIHBP1 GPLD1 GPX1 GPX3 GUSB GYG1 H6PD HADHA HAS2 HAS3 HJV HK1 HK2 HMGCS2 HPGDS HPSE2 HPSE HS3ST1 HSD11B1 HSPG2 ICAM1 IDH2 IGF2R IL18R1 IL1R1 IL1RAP IL1RL1 INPP5D INPP5K ISYNA1 ITLN1 ITPK1 KL KLRK1 LCAT LCT LDHA LEPR LGALS2 LGALS3 LIPA LIPC LIPG LMAN1 LPCAT3 LPL LSS LTA4H LTC4S LYZ MAG MBL2 MCFD2 MGAM MGLL MICA MMP17 MPI MRC1 MTAP NAAA NAGLU NAMPT NANS NCAM1 NDST4 NDUFAB1 NEU1 NT5E OGA OGDH OGG1 OLR1 OXCT1 PAFAH2 PARP12 PARP1 PARP2 PARP3 PC PCYT1A PCYT1B PDHA1 PEMT PFKFB3 PFKL PFKM PGM1 PIGF PIK3C2A PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKM PLA2G10 PLA2G15 PLA2G1B PLA2G2A PLA2G2D PLA2G4A PLA2G5 PLA2G6 PLA2G7 PLAUR PLB1 PLCD1 PLCD3 PLCG1 PLCG2 PLPP3 PNP PNPLA2 PNPLA3 PPARA PPP1R3B PRKAA2 PRNP PTEN PTGDS PTGES PTGIS PTGS1 PTGS2 PYGB PYGM RBP4 RENBP RGN RPN1 SACM1L SCD SDC1 SDC4 SELE SELENOI SELL SELP SEMA7A SFTPA1 SFTPA2 SFTPD SGMS2 SGPL1 SI SIGLEC1 SIRT2 SIRT4 SIRT6 SLC17A5 SLC2A12 SLC2A3 SLC2A4 SLC33A1 SLC35A1 SLC35G1 SLC39A8 SLC5A1 SMC3 SMPD1 SMPD2 SMPD3 SMUG1 SOAT1 SOAT2 SPHK1 SPHK2 SRGN ST3GAL4 ST6GAL1 ST6GALNAC5 ST8SIA1 ST8SIA4 STS SUCLA2 SULT1E1 TBXAS1 TLR4 TM7SF2 TNF TP53 TPI1 TYMP UGCG UGT1A1 UGT1A6 UMOD UMPS VCAM1 VCAN VNN1	10038 10039 100507436 1012 10135 10159 10162 10327 10400 10462 10466 10555 10559 1056 10682 10715 10724 10855 10965 1113 1116 1118 113026 11332 11343 120227 124 124872 125 126 128 1312 1374 1376 139189 142 1431 144423 1462 148738 151056 154091 1543 1544 1545 155 1555 1557 1558 1559 1571 1573 1576 1577 1579 1581 1585 1586 1588 1589 1593 159371 1594 1605 1634 1636 166929 1717 1718 1737 1738 176 189 1890 1946 2053 2137 217 2180 219 2215 2219 2220 2224 226 22796 22908 22914 22918 22933 231 23171 2331 23409 2350 23545 23583 23659 239 240 246 247 249 2525 2530 2539 2571 2583 2590 2591 2597 26279 2645 26503 2678 2683 27087 2710 27163 27306 2739 2752 28 2821 2822 283420 2876 2878 2990 2992 3030 3037 3038 308 3098 3099 31 3158 32 3290 3339 3383 338328 339221 340075 3418 3482 35 353 3554 3556 3635 3705 38 39 3931 3938 3939 3953 3957 3958 3988 3990 3992 3998 4023 4047 4048 4056 4069 4099 410 411 412 414 4153 43 432 4326 4329 4351 4360 4507 4669 4684 47 4706 4758 4860 4907 4967 4968 4973 5019 5051 5067 5091 51266 5130 51477 51548 5160 5167 51763 51809 5209 5211 5213 5236 5281 5286 5290 5291 5293 5294 5310 5315 5319 5320 5321 5322 5329 5333 5335 5336 54187 54578 5465 54658 54898 55512 5552 55600 5563 55902 55997 5621 56848 57016 57104 57124 5728 5730 5740 5742 5743 57511 5834 5837 5950 5973 60495 6184 6319 6382 6385 6401 6402 6403 64116 64174 64180 6441 64579 64581 6476 64761 6480 6484 6489 6515 6517 6523 653509 6609 6610 6614 6646 6783 6916 7099 7108 7124 7157 7167 729238 7357 7369 7372 7412 7903 79071 7941 79660 80339 811 81849 821 83539 8398 8399 8435 847 8482 8529 85465 8547 8613 8693 8694 8803 8809 8876 8877 8879 8972 9023 90411 9104 912 9126 9173 9197 9254 929 9365 9370 9388 93978 9415 9468 9469 9514 9536 9563 960 972 9957	Homo sapiens (human)
DOID:2436	glomangioma Aliases: Glomuvenous Malformation	SDHB SDHD	6390 6392	Homo sapiens (human)
DOID:14115	toxic shock syndrome Aliases: TSS toxic shock	ACE ENO2 FCGR3B FUT2 HSPG2 MBL2 SELL SLC5A1 TNF	1636 2026 2215 2524 3339 4153 6402 6523 7124	Homo sapiens (human)
DOID:0080123	mitochondrial DNA depletion syndrome 4b Aliases: mitochondrial neurogastrointestinal encephalopathy syndrome	TYMP	1890	Homo sapiens (human)
DOID:13810	familial hypercholesterolemia Aliases: Fredrickson type IIa hyperlipoproteinemia Fredrickson type IIa lipidaemia familial hyperbetalipoproteinaemia familial hypercholesteremia hyperbetalipoproteinemia type II hyperlipidemia	ABO ACE ACSS2 ADH1A ADPRH ALOX5 ANXA5 BAAT CH25H COG2 COL9A2 CYP7A1 EPHX2 EXT1 EXT2 GK GLB1 HSPG2 ICAM1 LCAT LIPA LIPC LIPG LPL OLR1 PLA2G15 PLA2G7 PRKCSH RBP4 SDC2 SELE SIGLEC7 TNFRSF10C	124 1298 141 1581 1636 2053 2131 2132 22796 23659 240 27036 2710 2720 28 308 3339 3383 3931 3988 3990 4023 4973 5589 55902 570 5950 6383 6401 7941 8794 9023 9388	Homo sapiens (human)
DOID:4188	echolalia	ATP6AP2 HGSNAT SLC35C1	10159 138050 55343	Homo sapiens (human)
DOID:614	lymphopenia Aliases: Lymphocytopenia	ACE ADH1B AGPS ALDH2 B3GAT1 EXTL3 G6PC3 LGALS8 PARP2 PGM3 PKD1 PLA2G10 PNP SGPL1 SIRT6 SLC17A5 SPHK1 SPHK2 TNF	10038 125 1636 2137 217 26503 27087 3964 4860 51548 5238 5310 56848 7124 8399 8540 8877 8879 92579	Homo sapiens (human)
DOID:720	normocytic anemia Aliases: ANEMIA NORMOCYTIC	ACHE ALDOA BPGM HK1 TPI1	226 3098 43 669 7167	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:5823	childhood lymphoma Aliases: pediatric lymphoma	ABO ACE ACOX1 ACSF3 ALOX12 ALPI ALPP ANXA5 CAT CD14 CD1D CD22 CD33 CD38 CD44 CD48 CD55 CD74 CEL CHGA CLEC10A CNTN2 COMT CYP17A1 CYP1A1 ENO2 ENOSF1 EPM2A FCER2 FCGR3B FH FMOD G6PD GBA1 GLB1 GPI GPX1 HEXA HMMR HPGDS HYAL2 ICAM1 IDH1 IDH2 IL1R1 IL1RL1 INPP4B INPP5D ISYNA1 KLRC1 KLRD1 KLRK1 LGALS1 LGALS3 LY6K MCAT MLYCD MRC1 MTAP NCAM1 NDUFAB1 NT5E PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PNP PPP1R3A PTEN PTGDS PTGES PTGS2 RTN4R SLC27A5 SLC2A3 SLC35A2 SLC35B2 SMC3 SMUG1 SOAT1 SPHK2 STS SULT1E1 TIGAR TMTC3 TNFRSF10C VCAM1 VTCN1	10462 1056 10998 1113 1312 1543 1586 1604 160418 1636 197322 2026 2208 2215 2271 22914 2331 23417 23583 239 248 250 2539 2629 2720 27306 27349 28 2821 2876 3073 308 3161 3383 3417 3418 347734 3554 3635 3821 3824 3956 3958 412 4360 4507 4684 4706 4860 4907 51 51477 5290 5291 5293 5294 54742 5506 55556 56848 57103 5728 5730 5743 65078 6515 6646 6783 6900 7355 7412 7957 79679 83666 847 8692 8794 8821 912 9126 9173 929 933 945 952 9536 960 962 972	Homo sapiens (human)
DOID:3650	lactic acidosis	ACADM ACADVL ACAT1 AGK AGXT ALDH6A1 ALDH7A1 ALDOB AMT BCKDHA BCKDHB CHAT CYP11A1 CYP11B2 CYP27B1 DBT DLAT DLD ECHS1 FBP1 FH G6PC1 GALT GCDH GLYCTK HADH HADHA HADHB HIBCH HMGCL HSD3B2 ICAM1 LCT MCEE MLYCD OGDH PC PCCA PCCB PCK1 PDHA1 PDHB PDHX PTGS1 PYGL SDHA SLC2A2 SLC37A4 SLC3A1 SLC5A1 SUCLA2 SUCLG1	1103 132158 1583 1585 1594 1629 1737 1738 189 1892 2203 2271 229 23417 2538 2542 2592 26275 2639 275 3030 3032 3033 3155 3284 3383 34 37 38 3938 4329 4967 501 5091 5095 5096 5105 5160 5162 55750 5742 5836 593 594 6389 6514 6519 6523 8050 84693 8802 8803	Homo sapiens (human)
DOID:6171	uterine carcinosarcoma Aliases: mixed mullerian sarcoma of uterus	L1CAM PIK3CA PTEN SMUG1	23583 3897 5290 5728	Homo sapiens (human)
DOID:9827	radioulnar synostosis	ALDH2 B3GAT3 B4GALT7 CHST3 COLEC10 COLEC11 EXT1 EXT2 HSPG2 MASP1 PIK3CA PRKAA2 SMC3 UMOD XYLT1	10584 11285 2131 2132 217 26229 3339 5290 5563 5648 64131 7369 78989 9126 9469	Homo sapiens (human)
DOID:11482	hemopericardium Aliases: Haemopericardium	ACADVL ACE ALG9 CAT GBA1 PMM2 PTGS2 SMUG1	1636 23583 2629 37 5373 5743 79796 847	Homo sapiens (human)
DOID:9245	Alagille syndrome Aliases: Alagille-Watson syndrome Arteriohepatic dysplasia	GGT1 NAAA	2678 27163	Homo sapiens (human)
DOID:0110584	autosomal dominant nonsyndromic deafness 6 Aliases: DFNA14 DFNA38 DFNA6 autosomal dominant deafness 14 autosomal dominant deafness 38 autosomal dominant deafness 6	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:5511	dysgerminoma of ovary Aliases: Ovarian Dysgerminoma	ACE PTEN	1636 5728	Homo sapiens (human)
DOID:4202	brain stem glioma Aliases: Brainstem Neuroglial tumor	DHDDS IDH1 IDH2 PIK3CA	3417 3418 5290 79947	Homo sapiens (human)
DOID:0110212	Charcot-Marie-Tooth disease X-linked recessive 4 Aliases: CMT4X CMTX4 Charcot-Marie-Tooth disease with deafness and mental retardation Cowchock syndrome NADMR NAMSD X-linked Charcot-Marie-Tooth disease type 4 axonal motor sensory neuropathy with deafness and mental retardation	ACE AMACR ARSA CANX CAT CD44 CYP4F3 DGAT2 FIG4 GBA1 GPX2 HADHB HK1 HPSE LCAT LPIN1 MAG MTM1 MTMR2 PGK1 PGM1 PLCB4 PLCE1 PRNP PRPS1 PTGS2 SIGLEC7 SPTLC1 SPTLC2	10558 10855 1636 23175 23600 2629 27036 2877 3032 3098 3931 4051 4099 410 4534 51196 5230 5236 5332 5621 5631 5743 821 84649 847 8898 9517 960 9896	Homo sapiens (human)
DOID:9521	Laron syndrome Aliases: Laron-type isolated somatotropin defect	ACAN ACER3 AGA AGL ALDH3A2 ALDOA ALOX12B ALPL ALPP ARSB ASAH1 ATP6V0A2 ATP6V1A ATRNL1 B3GALT6 B3GAT3 B4GALT7 CD38 CERS3 CHST3 CHSY1 COG4 COG5 COG7 COL9A2 COLEC10 COMT CRYL1 CSGALNACT1 CTNS CTSA CYP11B1 CYP17A1 CYP19A1 CYP27B1 CYP2B6 CYP2C19 CYP2C9 CYP2R1 DDOST DGCR2 DHCR24 DHCR7 DHDDS EBP EHHADH ENPP1 EXT1 EXT2 FIG4 FUCA1 FUT8 G6PC1 GALNS GAPDH GAS1 GBA1 GCK GFPT1 GK GLA GLB1 GM2A GMPPA GNPTAB GNPTG GPC3 GPD1 GUSB GYS2 H6PD HACD1 HPRT1 HSD11B2 HSD17B4 HSPG2 HYAL1 IDH1 IDH2 IDS IDUA INPP5K INPPL1 KDSR L1CAM LARGE1 LFNG MGAT2 MLYCD MSMO1 NEU1 OCRL OGDH PAPSS2 PCCA PCCB PCYT1A PGAP1 PGM1 PGM3 PIK3C2A PIK3CA PNPLA2 PNPLA6 PRPS1 PTDSS1 PTEN PYGL RFT1 SDHA SDHB SDHC SDHD SIRT6 SLC26A2 SLC2A2 SLC35A2 SLC35C1 SLC35G1 SLC37A4 SLC39A8 SMC3 SMPD1 SMPD3 SOAT1 STS SUCLA2 SULT1E1 SULT2B1 SUMF1 SYNJ1 TGDS TMEM165 UGDH VCAM1 XYLT1	10466 10584 10682 10908 11285 120227 126792 1298 1312 1497 1555 1557 1559 1584 1586 1588 159371 1594 1650 1717 1718 175 176 178 1836 1962 204219 2131 2132 224 226 22856 23417 23483 23545 242 249 250 2517 2530 2531 2538 2542 25839 2588 2597 26033 2619 26229 2629 2645 2673 2710 2717 2719 2720 2760 2819 285362 2990 29926 2998 3251 3291 3295 3339 3373 3417 3418 3423 3425 3636 3897 3955 411 412 4247 427 4758 4952 4967 5095 5096 51084 5130 51548 5167 51763 523 5236 5238 5286 5290 5476 55331 55343 55512 55790 55858 5631 57104 5728 5836 6307 6389 6390 6391 6392 64116 64131 6514 6609 6646 6783 6820 7355 7358 7412 79158 79947 80055 84572 8803 8867 9060 9126 91869 91949 9200 9215 9469 952 9563 9791 9896 9993	Homo sapiens (human)
DOID:6432	pulmonary hypertension	ACE ALOX5 CD209 CYP1A1 CYP2J2 DCN ENO1 EPHX2 HAS1 HAS2 HAS3 HK1 HYAL1 HYAL2 ICAM1 LGALS3 NAMPT PDIA3 PLA2G7 PTGIS PTGS2 SLC2A4 SMPD3 TNF VCAM1	10135 1543 1573 1634 1636 2023 2053 240 2923 3036 3037 3038 30835 3098 3373 3383 3958 55512 5740 5743 6517 7124 7412 7941 8692	Homo sapiens (human)
DOID:4773	congenital mesoblastic nephroma	GPC3	2719	Homo sapiens (human)
DOID:11161	neonatal respiratory failure Aliases: respiratory failure of newborn	SFTPC	6440	Homo sapiens (human)
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)
DOID:5530	thymus squamous cell carcinoma Aliases: Epidermoid Thymic carcinoma	LY75	4065	Homo sapiens (human)

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