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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 **6876 - 6900** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:0050886	Troyer syndrome Aliases: SPG20 autosomal recessive spastic paraplegia 20 autosomal recessive spastic paraplegia Troyer type autosomal recessive spastic paraplegia type 20 childhood-onset spastic paraparesis with distal muscle wasting hereditary spastic paraplegia 20 spastic paraplegia 20 spastic paraplegia type 20	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG NT5E PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 4907 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:0080547	metabolic dysfunction-associated steatohepatitis Aliases: MASH NASH non-alcoholic steatohepatitis nonalcoholic steatohepatitis	ACACA ACER3 CPT1A CYP27A1 CYP7A1 LEPR PCK1 SCD SPHK2 TNF	1374 1581 1593 31 3953 5105 55331 56848 6319 7124	Homo sapiens (human)
DOID:9675	pulmonary emphysema	ACE ATP6V0A2 CAT CD74 CEACAM5 CEACAM7 CH25H CHI3L1 CYP2B6 EPHX2 FDPS FUT8 GCLC GPX1 IL18R1 ISYNA1 KL LGALS9 LMAN2L MAN1C1 PARP1 PIK3CA PTEN PTGS2 RGN SFTPC SFTPD SGMS2 SIGLEC9 SLC2A10 SMPD2 SMPD3 SOAT1 TLR4 TM7SF2 VCAN	1048 1087 1116 142 1462 1555 1636 166929 2053 2224 23545 2530 27180 2729 2876 3965 51477 5290 55512 57134 5728 5743 6440 6441 6610 6646 7099 7108 81031 81562 847 8809 9023 9104 9365 972	Homo sapiens (human)
DOID:3818	photoallergic dermatitis Aliases: Photoallergic contact dermatitis Photoallergic eczema	AGPS	8540	Homo sapiens (human)
DOID:0111395	mucopolysaccharidosis type IIIA Aliases: MPS3A MPSIIIA Sanfilippo syndrome type A heparan sulfamidase deficiency mucopolysaccharidosis III-A mucopolysaccharidosis type 3A mucopolysaccharidosis type IIIA (Sanfilippo A)	ARSB CHAT EXT1 EXT2 EXTL2 EXTL3 GNS HGSNAT IDS IDUA NAGLU OGA SGSH SUMF1	10724 1103 138050 2131 2132 2135 2137 2799 285362 3423 3425 411 4669 6448	Homo sapiens (human)
DOID:7587	supraglottis squamous cell carcinoma Aliases: Epidermoid carcinoma of the Supraglottis	PTEN	5728	Homo sapiens (human)
DOID:0060708	lymphoproliferative syndrome 2 Aliases: CD27 deficiency LPFS2	ACSBG1 ASAH2 CD14 CD22 CD38 CD44 CEL CNTN2 EBP FCER2 FCGR3B FH ICAM1 IL18R1 IL1R1 KLRB1 KLRD1 LGALS1 MLYCD MRC1 NCAM1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PKM SDC1 SLC27A5 SLC35B2 SMUG1 SOAT1	1056 10682 10998 2208 2215 2271 23205 23417 23583 3383 347734 3554 3820 3824 3956 4360 4684 5290 5291 5293 5294 5315 56624 6382 6646 6900 83666 8809 929 933 952 960	Homo sapiens (human)
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	ACACA ACE ACHE ACO1 ACO2 ACOT7 ACSBG1 ADH1B ADH1C ADH4 ADH7 AKR1A1 AKT1 AKT2 ALDH2 ANXA5 APRT ARSA ASAH1 ATP6AP2 B3GALT4 B3GAT1 B4GALNT1 BST1 CALR3 CALR CAT CD14 CD38 CD44 CD55 CEACAM6 CEL CHAT CHI3L1 CHIT1 CNTN1 CNTN2 COMT CTNS CYP17A1 CYP1A1 CYP1A2 CYP1B1 CYP27B1 CYP2B6 CYP2C19 CYP2C9 CYP2E1 CYP3A5 CYP4F3 DCN DGKD DHRS11 DLD DPEP1 ELOVL7 ENO2 EPHX2 FASN FBP1 FBXO2 FCER2 FCGR3B FH G6PD GAD1 GAD2 GALC GALNS GAPDH GBA1 GBA2 GFPT1 GLA GLB1 GLUL GNPDA2 GPI GPNMB GPX1 GSK3B GSTO1 GSTO2 HAS2 HEXA HK1 HK2 HPGDS HSD17B6 HSD17B7 HSD3B7 ICAM1 IDUA IGF2 IGF2R INPP5F INPP5K ISYNA1 KL L1CAM LEP LGALS1 LGALS3 LGALS4 LYPD5 MAG MAPK14 MCAT MDGA2 MGLL MRC1 NAGLU NEIL1 NT5E NTM OGA OGG1 PAFAH1B1 PARP1 PDHA1 PDIA3 PGK1 PGK2 PGP PIGC PIK3C2B PIK3CA PIK3CB PIK3CD PIK3CG PISD PKD1 PLA2G1B PLA2G6 PLB1 PLD1 PLD2 PNPLA6 PPARGC1A PRKAA1 PRKAA2 PRNP PSAP PTEN PTGDS PTGES3 PTGES PTGIS PTGS2 RENBP RGMA RTN4R SARM1 SCD SDHA SHMT1 SHMT2 SI SIGLEC7 SIRT2 SLC17A5 SLC2A4 SLC33A1 SLC39A8 SMPD1 SMPD2 SMPD3 SMUG1 SOAT1 SPTSSB ST3GAL2 ST8SIA4 STBD1 SUCLA2 SYNJ1 SYNJ2 TALDO1 TIGAR TKT TM7SF2 TMED9 TNKS2 UGT1A9 UMOD VCAM1 XYLT2	10159 10327 10457 1056 10724 10728 10891 10908 1103 1116 1118 11332 11343 119391 125 125972 126 127 1272 131 1312 132789 142 1432 1497 151056 1543 1544 1545 1555 1557 1559 1571 1577 1586 1594 1604 161357 1634 1636 165679 1738 1800 2026 2053 207 208 217 2194 2203 2208 2215 2271 22876 22933 23098 23205 23583 23761 2539 2571 2572 2581 2583 2588 2597 26232 2629 26503 2673 27036 27087 2717 2720 27306 27349 2752 2821 283871 284348 2876 2923 2932 3037 3073 308 3098 3099 31 3383 3425 3481 3482 353 3897 3952 3956 3958 3960 4051 4099 410 427 43 4360 4669 4680 48 4907 4968 50 5048 50863 51477 51478 5160 51763 5230 5232 5279 5287 5290 5291 5293 5294 5310 5319 5337 5338 54600 54732 55512 5562 5563 5621 5660 56963 57103 5728 5730 5740 5743 57704 5973 6319 6389 64116 64132 6470 6472 6476 6483 65078 6517 6609 6610 6646 683 6888 6900 7086 7108 7369 7412 7903 79154 79661 79993 80270 80351 811 8398 847 8527 8630 8705 8803 8867 8871 8987 9197 929 9365 9446 952 9536 960	Homo sapiens (human)
DOID:12123	postinflammatory pulmonary fibrosis Aliases: Post-inflammatory pulmonary fibrosis	ACE ACO2 ANXA5 APRT ASAH1 ATP6AP2 B3GAT1 B3GAT3 CAT CD44 CEL CHAT CHI3L1 CHIT1 CHST15 CYP27B1 DCN ELOVL6 FASN FCGR3B FOLR2 FUT8 GLB1 HAS2 HPGDS ICAM1 IL1RL1 INPP5D KL LCLAT1 LDHA LGALS1 LGALS3 MPG MRC1 NEU1 NEU3 NT5E OGG1 PARP9 PIGN PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLAUR PRKAA2 PTEN PTGS2 SDC1 SDC2 SDC4 SELE SEMA7A SFTPA1 SFTPA2 SFTPC SFTPD SGPL1 SIRT6 SLC27A5 SMUG1 SOAT1 SPHK2 SULF1 SULF2 TM7SF2 VCAM1	10159 1056 10825 10998 1103 1116 1118 1594 1634 1636 2194 2215 23213 2350 23556 23583 2530 253558 26229 27087 2720 27306 3037 308 3383 353 3635 3939 3956 3958 427 4350 4360 4758 4907 4968 50 51363 51548 5290 5291 5293 5294 5321 5329 5563 55959 56848 5728 5743 6382 6383 6385 6401 6440 6441 653509 6646 7108 729238 7412 79071 83666 847 8482 8879 9173 9365 960	Homo sapiens (human)
DOID:14110	anus cancer Aliases: anal cancer malignant anal tumor	CEACAM5 LIPA PIK3CA PIK3CB PIK3CD PIK3CG SMUG1	1048 23583 3988 5290 5291 5293 5294	Homo sapiens (human)
DOID:2632	papillary serous adenocarcinoma Aliases: Micropapillary serous carcinoma Papillary serous carcinoma serous surface papillary carcinoma	CEACAM5 CEACAM7	1048 1087	Homo sapiens (human)
DOID:2256	osteochondrodysplasia Aliases: Cartilage Development disorder Congenital anomaly of cartilage Osteochondrodysplasia syndrome chondrodystrophy skeletal dysplasia	ACAN ACHE AKR1B1 ALDH3A2 ALG9 ALPL ARSB B3GAT3 B4GALT7 CD38 CHST1 CHST3 COL9A2 CTSA CYP27B1 CYP2B6 CYP2C19 CYP2C9 DCN EBP ENPP1 EXTL3 GALNS GLB1 GNPTAB GNPTG HS6ST1 HSPG2 HYAL1 IDS IDUA LFNG MICA NAGLU NANS NEU1 PAPSS2 PGM3 PTEN SGSH SLC26A2 SLC35A3 SLC35D1 SMUG1 SPAM1 XYLT1	100507436 10682 11285 1298 1555 1557 1559 1594 1634 176 1836 2137 224 231 23169 23443 23583 249 2588 26229 2720 3339 3373 3423 3425 3955 411 43 4669 4758 5167 5238 54187 5476 5728 64131 6448 6677 79158 79796 84572 8534 9060 9394 9469 952	Homo sapiens (human)
DOID:7004	ACTH-secreting pituitary adenoma Aliases: ACTH-Producing Pituitary Adenoma Corticotroph adenoma Corticotropinoma	CD14 CNTN3 CYP11B1 GAPDH HSD11B1 HSD11B2 SMUG1	1584 23583 2597 3290 3291 5067 929	Homo sapiens (human)
DOID:10534	stomach cancer Aliases: gastric cancer gastric neoplasm	A4GNT ABO ACACA ACE ACHE ACLY ACO2 ACSL4 ACSS2 ACSS3 ACYP2 ADH1A ADH1B ADH1C ADH4 ADH5 ADH6 ADH7 AGA AKR1A1 AKR1B10 AKR1B1 AKR1C3 ALDH1A3 ALDH2 ALDH3A1 ALDH7A1 ALDOB ALOX12 ALOX15 ALOX5 ALPP AMY2A ANXA4 ANXA5 ANXA7 APRT ARSF ARSI ATP6V1A B3GAT1 BAAT BST2 CACNA2D1 CACNA2D3 CALR CANX CAT CBR1 CD14 CD177 CD1D CD248 CD33 CD44 CD55 CD74 CDH13 CEACAM5 CEACAM6 CEACAM7 CEMIP CERS6 CHGA CHI3L1 CHPT1 CLEC1B CNTN1 COG2 COG8 COMT CPT1A CYP19A1 CYP1A1 CYP1A2 CYP2B6 CYP2C19 CYP2E1 CYP3A4 CYP4F3 DCN DHDDS DHRS11 DLD DPAGT1 EBP ECHS1 EFNA1 EFNA2 ENO1 ENOSF1 FADS1 FADS2 FASN FBP1 FBP2 FBXO2 FH FKTN FOLR1 FOLR2 FUT11 FUT1 FUT2 FUT3 FUT4 FUT5 FUT6 GAL3ST1 GALE GALNS GALNT1 GALNT2 GALNT5 GALNT6 GAPDH GAS1 GBA3 GFPT1 GGT1 GLB1 GLDC GLO1 GLUL GOLPH3 GPAA1 GPC3 GPI GPNMB GPX1 GPX2 GPX3 GUSB HACD1 HAS1 HK1 HK2 HMMR HPGDS HPSE HS6ST2 HSD11B2 HSD17B1 HSD17B2 HSD17B7 HSD3B1 ICAM1 ICAM2 IDH1 IDH2 IDH3B IDUA IGF2R IL18R1 IL1RL1 IL6ST INPP5K INPPL1 ISYNA1 ITLN1 KLRK1 L1CAM LDHA LGALS1 LGALS2 LGALS3 LGALS9 LIPF LMAN2 LYPD5 LYZ MBD4 MBL2 MBOAT7 MCAT MDGA2 MELTF MGAT5 MICA MMP25 MMUT MRC1 MSLN MTAP MTMR2 MTMR3 MUTYH NAGLU NAMPT NANS NCAM1 NEIL1 NEIL2 NEU1 NEU2 NGLY1 NT5E NTHL1 OARD1 OGG1 OGT OPCML PARP1 PCCA PCNA PDHA1 PDIA3 PFKFB1 PFKFB2 PFKFB3 PFKFB4 PGAM1 PGAP3 PGK1 PIK3CA PIK3CB PIK3CD PIK3CG PIP5KL1 PKD1 PKM PLA2G2A PLAUR PLCD1 PLCE1 PLCG2 PLD1 PLPP1 PNPLA2 PPAT PRKAA2 PRNP PSAP PSMD10 PTEN PTGDS PTGS1 PTGS2 RECK RGN RPN2 SARM1 SDC1 SDHA SDHB SDHC SDHD SELE SELL SGPP1 SGPP2 SHMT2 SIRT2 SIRT4 SIRT6 SLC26A2 SLC2A4 SLC35B4 SMUG1 SOAT1 SPHK1 ST3GAL3 ST3GAL6 ST6GAL1 ST6GALNAC1 STS SUCLG1 SULF1 SULF2 SULT1E1 TDG TFF1 TIGAR TKT TKTL1 TM7SF2 TMED6 TMEM260 TNKS TP53 TPI1 TYMP UGCG UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B15 ULBP1 UMPS UPP1 VCAM1 VCAN VTCN1	100507436 1012 10135 10232 10327 10402 10457 1048 10682 10855 1087 10960 1113 1116 11226 11227 124 125 126 127 1272 128 130 130367 131 1312 1374 138429 142 1462 146456 1543 1544 1555 1557 1571 1576 1588 1604 161357 1634 1636 170384 1738 175 1798 1836 1890 1892 1942 1943 2023 217 218 2182 2194 220 2203 221443 2218 2271 22796 229 22914 22933 23098 231 23213 23409 2348 2350 23583 239 240 246 250 2523 2524 2525 2526 2527 2528 252969 253782 2582 2588 2589 2590 2597 2619 26232 2673 2678 27087 2719 2720 27306 2731 27349 2739 2752 279 28 2821 284348 2876 2877 2878 2923 2990 3036 307 308 3098 3099 31 310 3161 3283 3291 3292 3294 3383 3384 340075 3417 3418 3420 3425 3482 353 3572 3636 3897 3939 3956 3957 3958 3965 3992 4051 4069 412 4153 416 4241 4249 43 4360 4507 4594 4595 4669 4680 4684 47 4758 4759 4907 4913 4968 4978 50 501 5095 5111 51146 51196 51266 51477 51478 51548 5160 51763 5207 5208 5209 5210 5223 523 5230 5290 5291 5293 5294 5310 5315 5320 5329 5333 5336 5337 54187 54575 54576 54577 54578 54600 54657 54658 5471 54916 55556 55600 5563 55768 55799 55808 55902 55959 5621 5660 56994 570 57016 57103 57104 57124 57126 5716 57214 5728 5730 5742 5743 57733 6185 6382 6389 6390 6391 6392 6401 6402 64083 64386 6472 6480 6487 6517 6646 6783 684 6996 7031 7086 7108 7157 7167 7357 7366 7372 7378 7412 781 79143 79154 79611 79661 79679 79947 80329 811 81537 821 8277 8434 84342 847 8473 84912 8513 8611 8644 8658 873 8733 8789 8802 8809 8877 8897 8898 8930 90161 9104 912 9173 9200 929 93210 9415 945 9514 960 972 98	Homo sapiens (human)
DOID:0050559	Fukuyama congenital muscular dystrophy	B3GALNT2 B4GAT1 CD109 CRPPA DAG1 FKRP FKTN GMPPB LARGE1 POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1	10329 10585 11041 135228 148789 1605 2218 29925 29954 55624 729920 79147 84197 84892 9215	Homo sapiens (human)
DOID:0081331	glycogen storage disease Ic	SLC37A4	2542	Homo sapiens (human)
DOID:5292	mediastinum leiomyosarcoma Aliases: leiomyosarcoma of mediastinum	SMUG1	23583	Homo sapiens (human)
DOID:13087	Lown-Ganong-Levine syndrome Aliases: atrial tachyarrhythmia with short PR interval syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias	APRT ARSD B3GAT1 CNTN2 FCGR3B PRKAA2	2215 27087 353 414 5563 6900	Homo sapiens (human)
DOID:0110814	hereditary spastic paraplegia 63 Aliases: SPG63 autosomal recessive spastic paraplegia 63 spastic paraplegia 63	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:2691	myoma Aliases: benign neoplasm of the Muscle	CYP19A1 CYP2B6 HPSE	10855 1555 1588	Homo sapiens (human)
DOID:341	peripheral vascular disease Aliases: arterial occlusive disease	ABO ACE AGXT ALDH7A1 CALR CD14 CHI3L1 CYP1A1 CYP1A2 CYP2C19 DLD EFNA5 ENPP1 GPX1 ICAM1 IGF2R LIPC MBL2 NT5E PCYT1A SELL SLC2A10 SRD5A1 STS VCAM1	1116 1543 1544 1557 1636 1738 189 1946 28 2876 3383 3482 3990 412 4153 4907 501 5130 5167 6402 6715 7412 81031 811 929	Homo sapiens (human)
DOID:11554	Chandler syndrome Aliases: Chandler's syndrome Dystrophy of corneal endothelium Endothelial corneal dystrophy Posterior membrane corneal dystrophy	NEIL1 PIK3CA PIK3CB PIK3CD PIK3CG	5290 5291 5293 5294 79661	Homo sapiens (human)
DOID:10314	endocarditis	ACE APRT ARSD CALR CHPT1 CS ENO1 G6PD GPI ICAM1 MANEA MTM1 PCYT1A SMUG1	1431 1636 2023 23583 2539 2821 3383 353 414 4534 5130 56994 79694 811	Homo sapiens (human)
DOID:0080190	malignant epithelioid hemangioendothelioma	SMUG1	23583	Homo sapiens (human)
DOID:11724	limb-girdle muscular dystrophy Aliases: Erb's muscular dystrophy Leyden-Mbius muscular dystrophy limb girdle muscular dystrophy	ACAN ACE ACHE AGK AGL ALDH7A1 ALOX12 ALPP APRT ATRNL1 B3GALNT2 B4GALNT2 B4GAT1 CD44 CHKA CHKB CRPPA CTNS DAG1 DCN DPEP1 DPM1 DPM2 DPM3 ENO1 FKRP FKTN GAA GK GLB1 GMPPB GNE HACD1 HPGDS HSPG2 IDH2 IMPA1 INPP5B INPP5K LARGE1 LARGE2 LGALS3 MBL2 MGAM PARP1 PIK3C2A PMM2 POGLUT1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PRG2 PRKAA2 PYGM RGN RXYLT1 SDC2 SI SIRT2 SLC3A1 ST3GAL4 SYNJ1 SYNJ2	10020 10329 10585 11041 1119 1120 120071 124872 142 148789 1497 1605 1634 1636 176 178 1800 2023 2218 22933 239 250 2548 26033 2710 2720 27306 29925 29954 3339 3418 353 3612 3633 3958 4153 43 501 51763 5286 5373 54344 5553 55624 5563 55750 56983 5837 6383 6476 6484 6519 729920 79147 84197 84892 8813 8818 8867 8871 8972 9104 9200 9215 960	Homo sapiens (human)

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