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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 **2626 - 2650** of **4621** in total

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Disease ID	Disease Name ▲	Gene Symbol	Gene ID	Organism
DOID:0110817	hereditary spastic paraplegia 72A Aliases: SPG72 autosomal spastic paraplegia type 72	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:0110818	hereditary spastic paraplegia 73 Aliases: SPG73 autosomal dominant spastic paraplegia 73 autosomal dominant spastic paraplegia type 73	B4GALNT1 CPT1C CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 126129 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	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:0110822	hereditary spastic paraplegia 77 Aliases: SPG77 autosomal recessive spastic paraplegia 77	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:0110823	hereditary spastic paraplegia 8 Aliases: SPG8 autosomal dominant spastic paraplegia 8 autosomal dominant spastic paraplegia type 8	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:0112349	hereditary spastic paraplegia 81 Aliases: SPG81 autosomal recessive complex SPG due to Kennedy pathway dysfunction autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction spastic paraplegia 81 autosomal recessive	SELENOI	85465	Homo sapiens (human)
DOID:0112343	hereditary spastic paraplegia 82 Aliases: SPG82 spastic paraplegia 82 autosomal recessive	PCYT2	5833	Homo sapiens (human)
DOID:0112347	hereditary spastic paraplegia 84 Aliases: SPG84 spastic paraplegia 84 autosomal recessive	PI4KA	5297	Homo sapiens (human)
DOID:0070459	hereditary spastic paraplegia 90A Aliases: SPG90A autosomal dominant spastic paraplegia 90A	SPTSSA	171546	Homo sapiens (human)
DOID:0070460	hereditary spastic paraplegia 90B Aliases: SPG90B autosomal recessive spastic paraplegia 90B	SPTSSA	171546	Homo sapiens (human)
DOID:0110824	hereditary spastic paraplegia 9A Aliases: AD-SPG9A Cataracts motor neuropathy-short stature-skeletal anomalies syndrome SPG9A autosomal dominant complex spastic paraplegia type 9A autosomal dominant spastic paraplegia 9A cataracts with motor neuronopathy, short stature and skeletal abnormalities spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome	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:0110825	hereditary spastic paraplegia 9B Aliases: SPG9B autosomal recessive complex spastic paraplegia type 9B autosomal recessive spastic paraplegia 9B	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:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM L2HGDH MAG PCYT2 PLA2G6 PNPLA6 PNPLA7 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 375775 3897 4099 51302 57704 5833 79944 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	ACE CAT PTGS2	1636 5743 847	Homo sapiens (human)
DOID:12971	hereditary spherocytosis Aliases: Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia	ACE CAT CD55 G6PD GAPDH HK1 PGK1 PTGS2 ST8SIA4 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UMPS	1604 1636 2539 2597 3098 5230 54575 54576 54577 54578 54657 54658 5743 7372 7903 847	Homo sapiens (human)
DOID:3763	hermaphroditism	AKR1C1 AKR1C2 AKR1C3 AKR1C4 CDIPT CYP11A1 CYP11B1 CYP17A1 CYP19A1 CYP21A2 CYP2B6 DHCR24 DHRS11 GAS1 HSD17B3 HSD17B7 HSD3B1 HSD3B2 MECR PGD PKD2 PRSS21 SRD5A2	10423 10942 1109 1555 1583 1584 1586 1588 1589 1645 1646 1718 2619 3283 3284 3293 51102 51478 5226 5311 6716 79154 8644	Homo sapiens (human)
DOID:9976	heroin dependence	ABAT ADH1B ALDH2 COMT CYP2B6 CYP2C19 ENO2 GAD1 GAD2 HPGDS ICAM1 MDH2 NCAM1 NPY1R PARP9 PIK3CA PIK3CB PIK3CD PIK3CG RGMA	125 1312 1555 1557 18 2026 217 2571 2572 27306 3383 4191 4684 4886 5290 5291 5293 5294 56963 83666	Homo sapiens (human)
DOID:0080158	herpes simplex virus keratitis Aliases: dendritic keratitis	PIK3CA PIK3CB PIK3CD PIK3CG SFTPD TLR4	5290 5291 5293 5294 6441 7099	Homo sapiens (human)
DOID:8566	herpes simplex Aliases: Herpesvirus hominis disease	AKR1B1 ASAH1 CAT CD38 CD44 CEACAM5 CLEC9A COMT CTSA CYP1A1 CYP2B6 ENPP1 FASN FCGR3B FUT3 GAD1 GAD2 GLB1 GUSB HPRT1 HS3ST1 HS3ST6 ICAM1 LGALS1 LGALS4 LGALS9 MBL2 MRC1 MTMR3 MTMR4 PARG PIK3CA PIK3CB PIK3CD PIK3CG PNP PTGS2 SFTPC SMPD1 SOAT1 STT3A SUCLA2 TNKS TREH UNG XYLT2	1048 11181 1312 1543 1555 2194 2215 231 2525 2571 2572 2720 283420 2990 3251 3383 3703 3956 3960 3965 4153 427 4360 4860 5167 5290 5291 5293 5294 5476 5743 64132 6440 64711 6609 6646 7374 847 8505 8658 8803 8897 9110 952 960 9957	Homo sapiens (human)
DOID:8536	herpes zoster Aliases: Shingles herpes zona	ARSA CYP11A1 CYP17A1 ENOSF1 GP2 TECTA TNF	1583 1586 2813 410 55556 7007 7124	Homo sapiens (human)
DOID:12642	hiatus hernia Aliases: Diaphragmatic - hiatus -hernia hiatal hernia	ACE ACSS2 CHPT1 CHST14 CYP2C19 DCN DHDDS DSEL ECI1 FREM1 FUT3 ICAM1 NDST1 PLA2G15 SFTPC SLC2A10 VCAM1	113189 1557 158326 1632 1634 1636 23659 2525 3340 3383 55902 56994 6440 7412 79947 81031 92126	Homo sapiens (human)
DOID:2280	hidradenitis suppurativa Aliases: Acne inversa, familial	ANXA5 CHI3L1 CYP4F3 ELOVL7 IDH1 IDH2 IDH3B IL1RL2 KLRB1 SULT1E1 TNF	1116 308 3417 3418 3420 3820 4051 6783 7124 79993 8808	Homo sapiens (human)
DOID:2282	hidradenitis Aliases: Hydradenitis	ANXA5 CHI3L1 CYP4F3 ELOVL7 IDH1 IDH2 IDH3B IL1RL2 KLRB1 SULT1E1	1116 308 3417 3418 3420 3820 4051 6783 79993 8808	Homo sapiens (human)
DOID:3896	hidradenoma Aliases: Hidradenoma of skin Sweat gland adenoma Syringoadenoma	AMACR CD44 CEACAM5 CYP24A1 G6PD GALK1 GLB1 GPC3 HPSE ICAM1 LGALS3 LGALS9 MTAP NSDHL PARP1 PIK3CA PKD1 PKM PLA2G6 PLCB4 PTEN PTGS2 RECK SDHB SDHC SDHD SIRT6 STS VCAN	1048 10855 142 1462 1591 23600 2539 2584 2719 2720 3383 3958 3965 412 4507 50814 51548 5290 5310 5315 5332 5728 5743 6390 6391 6392 8398 8434 960	Homo sapiens (human)
DOID:3070	high grade glioma Aliases: Neuroglial tumor glial cell tumor glioma, malignant malignant Neuroglial tumor malignant glioma	ABO ACACA ACACB ACAT1 ACE ACHE ACLY ACOD1 ACOT7 ACSBG1 ACSL1 ACSL3 ACSL4 ACSL5 ACSS2 ACYP2 ADH1A ADH1B ADH1C ADH4 ADH6 AGK AGPS AGXT AKR1A1 AKR1B10 AKR1B1 AKR1C3 AKT2 ALDH1A3 ALDH3A1 ALDH7A1 ALG2 ALOX5 ALPI ALPP AMACR ANXA5 ANXA7 APRT ARF4 ARSA ART1 ASAH1 ATP6AP2 ATP6V0A2 ATRN B3GAT1 B4GALNT1 B4GALT5 BAAT BAD BCAN BDH1 BDH2 BRAF BST2 CACNA2D3 CALR CANX CAT CBR1 CD109 CD22 CD248 CD33 CD38 CD44 CD48 CD55 CD74 CD93 CDH13 CDS1 CEACAM5 CEACAM7 CERS1 CERS2 CH25H CHI3L1 CHKA CHPF CHPT1 CHST15 CHSY1 CHSY3 CLC CLEC18B CLEC5A CMAS CNTFR CNTN1 CNTN2 CNTN3 COL9A2 CPT1A CPT1C CS CSPG4 CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP27A1 CYP27B1 CYP2B6 CYP2C9 CYP2E1 CYP2J2 CYP46A1 CYP4F3 DAG1 DBT DCN DCTD DEGS1 DGKA DGKI DGKZ DHCR24 DHDDS DLD DPEP1 EBP ECHS1 EFNA1 EFNA2 ELOVL2 ENO1 ENO2 ENOSF1 ENPP1 ENPP2 EXT1 FADS2 FASN FBP1 FBXO17 FCN2 FDFT1 FDPS FIG4 FKTN FMOD FUT4 G6PC1 G6PD GAD1 GAL3ST1 GALNT14 GALNT2 GALNT7 GAPDH GAS1 GFPT1 GLB1 GLDC GLO1 GLUL GML GOLPH3 GPC1 GPC5 GPD1 GPD2 GPI GPIHBP1 GPNMB GPX1 GPX3 HACD1 HAS2 HEXA HEXB HJV HK1 HK2 HMMR HPGDS HPSE HSD3B7 HSPG2 HYAL1 HYAL2 HYAL3 ICAM1 IDH1 IDH2 IDUA IL18R1 IL1R1 IMPA1 INPP5K INPPL1 ISYNA1 ITPKA KHK KL KLRK1 L1CAM L2HGDH LAYN LDHA LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LPL LSS LYZ MAG MAN2A1 MBD4 MBL2 MCAT ME1 ME2 MELTF MGAT1 MGAT5 MICA MMUT MPG MPI MRC1 MSLN MTAP MTMR3 MUTYH NAMPT NANS NCAM1 NDST1 NEU1 NEU3 NEU4 NT5E OCRL OLR1 OPCML OXCT1 PAFAH1B1 PARG PARP1 PARP3 PCYT1A PDIA3 PFKFB2 PFKFB3 PFKFB4 PFKM PGAM1 PGK1 PIK3C2B PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PKD1 PKD2 PKM PLA2G10 PLA2G2A PLA2G4A PLA2G4C PLA2G5 PLAUR PLB1 PLCB1 PLCG1 PLD1 PLD2 PLEKHA8 PLOD3 PLPP1 PLPP3 PNLIP PNP PNPLA2 POMGNT1 PPT1 PRKAA2 PRNP PRPS1 PRSS8 PSAP PSMD10 PTEN PTGDS PTGES PTGS1 PTGS2 QPRT RECK RTN4R SCD SDC1 SDC2 SDC4 SDHA SDHB SDHC SDHD SELP SEMA7A SGMS1 SGMS2 SGPL1 SHMT2 SIGLEC7 SIGLEC9 SIRT2 SIRT6 SLC2A3 SLC2A5 SLC35A1 SLC35A3 SLC35F1 SLC37A4 SLC3A1 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 SPTLC1 SRD5A1 SRGN ST6GAL1 ST6GALNAC5 ST8SIA1 ST8SIA2 ST8SIA4 STS SUCLG1 SULF1 SULF2 SULT1E1 SYNJ1 TDG THEM4 TIGAR TKT TKTL1 TM7SF2 TMED5 TNF TNFRSF10C TNKS TP53 TPI1 TREH TUSC3 TYMP UGCG UGDH UGP2 UGT8 UNG VCAM1 VCAN VNN2 VTCN1 XYLT1	10039 100507436 1012 10135 10159 10232 10327 1040 10457 1048 10558 10559 10682 10715 10825 10855 10858 1087 1116 11181 1119 11332 115290 117145 1178 124 125 126 126129 127 1271 1272 1298 129807 130 135228 1374 142 1431 143903 1462 1464 148738 151056 1543 1545 1555 1559 1571 1573 1586 1588 1593 1594 1604 1605 1606 1629 1634 1635 1636 166929 1718 1738 1800 189 1890 1892 1942 1943 2023 2026 208 2131 218 2180 2181 2182 2194 220 2203 2218 2220 2222 2224 222553 2262 22856 22914 22918 22933 231 23205 23213 23236 2331 23443 23475 23545 23583 23600 23601 240 248 250 2526 2538 2539 2542 2571 2583 2590 259230 2597 2619 2673 27036 27087 27180 2720 27306 2731 27349 2739 2752 2765 28 2817 2819 2820 2821 2876 2878 2923 29956 3037 3073 3074 308 3098 3099 31 310 3161 32 3339 3340 3373 337876 3383 338328 3417 3418 3425 353 3554 3612 3636 3706 378 3795 38 3897 3939 3956 3958 3960 3964 3965 4023 4047 4051 4069 4099 410 412 4124 4153 417 4199 4200 4241 4245 4249 427 43 4350 4351 4360 4507 4594 4595 4684 47 4758 4860 4907 4952 497190 4973 4978 501 5019 5048 5067 50999 5130 51363 51477 51548 5167 5168 51703 51763 51809 5208 5209 5210 5213 5223 5230 5287 5289 5290 5291 5293 5294 5305 5310 5311 5315 5320 5321 5322 5329 5335 5337 5338 5406 54187 54898 5538 5552 55556 55624 5563 55750 55799 55902 55907 55959 5621 5631 5652 5660 56848 56898 56994 570 57016 57103 57104 57124 5716 572 5728 5730 5742 5743 622 6319 6382 63827 6383 6385 6389 6390 6391 6392 6403 64083 64131 6472 6480 6489 65078 6515 6518 6519 6609 6646 6715 673 6783 684 6900 6996 7086 7108 7124 7157 7167 730249 7357 7358 7360 7368 7374 7412 7903 79586 79623 79679 7991 79944 79947 80270 811 8128 81849 821 8277 8372 8399 8434 8455 847 84725 8482 8505 8525 85365 8540 8560 8605 8611 8613 8644 8658 8692 873 8794 8802 8809 8867 8875 8877 8879 8897 8930 8985 9023 9162 9200 933 9334 9365 9415 945 9514 952 9536 960 962 972 98 9896	Homo sapiens (human)

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