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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 **2026 - 2050** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:0110717	Warburg micro syndrome 2 Aliases: Micro Syndrome 2 WARBM2	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:0090001	Fraser syndrome Aliases: cryptophthalmos with other malformations	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: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:0110719	Warburg micro syndrome 4 Aliases: Micro Syndrome 4 WARBM4	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:0110718	Warburg micro syndrome 3 Aliases: Micro Syndrome 3 WARBM3	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:0060599	Nance-Horan syndrome	AKR1C4 CNTN3 COG1 CYP2B6 DGCR2 FREM1 G6PD GAS1 LSS NT5E SLC26A2	1109 1555 158326 1836 2539 2619 4047 4907 5067 9382 9993	Homo sapiens (human)
DOID:0060703	Muenke Syndrome Aliases: FGFR3-related craniosynostosis	AKR1C4 CNTN3 COG1 CYP2B6 DGCR2 FREM1 G6PD GAS1 LSS NT5E SLC26A2	1109 1555 158326 1836 2539 2619 4047 4907 5067 9382 9993	Homo sapiens (human)
DOID:0090091	hypogonadotropic hypogonadism 23 with or without anosmia Aliases: 46,XY DSD due to LHB deficiency 46,XY DSD due to luteinizing hormone subunit beta deficiency 46,XY disorder of sex development due to LHB deficiency 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency Pasqualini syndrome fertile eunuch syndrome leydig cell hypoplasia due to LHB deficiency	AKR1C2 AKR1C4 CHST3 CYP11A1 CYP17A1 DHRS11 HSD17B3 HSD17B7 HSD3B2 SRD5A2	1109 1583 1586 1646 3284 3293 51478 6716 79154 9469	Homo sapiens (human)
DOID:0111773	46,XY sex reversal 8 Aliases: SRXY8 TDD male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase	AKR1C2 AKR1C4	1109 1646	Homo sapiens (human)
DOID:0050012	chikungunya Aliases: Chikungunya fever	AKR1C4 BST2 CD209 CD74 FASN GOLPH3 KLRD1 MPG NCAM1 NDST1 PIK3CA PIK3CB PIK3CD PIK3CG SIGLEC9 SMUG1 SPHK2	1109 2194 23583 27180 30835 3340 3824 4350 4684 5290 5291 5293 5294 56848 64083 684 972	Homo sapiens (human)
DOID:8805	intermediate coronary syndrome Aliases: Angina at rest Anginal chest pain at rest Impending infarction Preinfarction angina Unstable angina Worsening angina	ACE AKT1 ARSA CD14 CHGA CHI3L1 CYP2C19 ICAM1 IL18R1 LGALS3 MBL2 PARP1 PLA2G1B PLB1 PTEN PTGS2 SELP SULT1E1	1113 1116 142 151056 1557 1636 207 3383 3958 410 4153 5319 5728 5743 6403 6783 8809 929	Homo sapiens (human)
DOID:660	adrenal cortex cancer Aliases: Adrenal cortical tumors malignant Adrenocortical tumor malignant neoplasm of adrenal cortex malignant tumour of adrenal cortex neoplasm of adrenal cortex	ACACA ACADVL ACAT1 ACOT7 AKR1B10 AKR1B1 AKR1C3 ALOX15B CD22 CHGA CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP21A2 CYP2B6 CYP4F2 CYP4F3 DHCR24 ENO2 ENPP3 FH G6PD GAPDH GLB1 HSD11B2 HSD17B4 HSD3B2 IDH1 IDH2 IGF2R MDH2 MUTYH NAGLU PIK3CA PLCB3 PTEN SCP2 SDHB SDHC SDHD SIRT6 SMUG1 SOAT1 SPHK1 TKT TM7SF2	1113 11332 1555 1583 1584 1585 1586 1588 1589 1718 2026 2271 231 23583 247 2539 2597 2720 31 3284 3291 3295 3417 3418 3482 37 38 4051 4191 4595 4669 51548 5169 5290 5331 57016 5728 6342 6390 6391 6392 6646 7086 7108 8529 8644 8877 933 9469	Homo sapiens (human)
DOID:3948	adrenocortical carcinoma Aliases: Adrenal cortical carcinoma carcinoma of the Adrenal cortex	ACACA ACAT1 ACOT7 AKR1B1 AKR1C3 CD22 CHGA CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP2B6 CYP4F2 DHCR24 ENO2 ENPP3 FH GLB1 HSD17B4 IGF2R MDH2 MUTYH NAGLU PIK3CA PLCB3 SCP2 SDHB SDHD SIRT6 SOAT1 SPHK1 TM7SF2	1113 11332 1555 1583 1584 1585 1586 1588 1718 2026 2271 231 2720 31 3295 3482 38 4191 4595 4669 51548 5169 5290 5331 6342 6390 6392 6646 7108 8529 8644 8877 933 9469	Homo sapiens (human)
DOID:3950	adrenal carcinoma Aliases: carcinoma of the Adrenal gland	ACACA ACAT1 ACOT7 AKR1B1 AKR1C3 CD22 CHGA CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP2B6 CYP4F2 DHCR24 ENO2 ENPP3 FH GLB1 HSD17B4 IGF2R MDH2 MUTYH NAGLU PIK3CA PLCB3 SCP2 SDHB SDHD SIRT6 SOAT1 SPHK1 TM7SF2	1113 11332 1555 1583 1584 1585 1586 1588 1718 2026 2271 231 2720 31 3295 3482 38 4191 4595 4669 51548 5169 5290 5331 6342 6390 6392 6646 7108 8529 8644 8877 933 9469	Homo sapiens (human)
DOID:0060185	Clostridium difficile colitis Aliases: Pseudomembranous colitis	ABO ACACB ACE ACHE ACSBG1 AGA AKR1B1 ARSA CAT CD14 CEACAM6 CHGA COMT CYP2B6 CYP4F3 FCN1 GLB1 GLUL GM2A HSD11B1 HSD11B2 ICAM1 IL18R1 KLB LCT MBL2 NCAM1 PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PTGS2 SELE SELL SFTPC SI SLC26A2	1113 1312 152831 1555 1636 175 1836 2219 231 23205 2720 2752 2760 28 2923 32 3290 3291 3383 3938 4051 410 4153 43 4680 4684 5290 5291 5293 5294 5315 5743 6401 6402 6440 6476 847 8809 929	Homo sapiens (human)
DOID:11569	neurocirculatory asthenia Aliases: Cardiovascular malfunction arising from mental factors Cardiovascular neurosis Da Costa's syndrome Krishaber's disease	ACE ACHE ACSBG1 AGA AKR1B1 ARSA CAT CD14 CEACAM6 CHGA COMT CYP2B6 CYP4F3 GLB1 GLUL HSD11B1 HSD11B2 IL18R1 KLB LCT MBL2 PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PTGS2 SI SLC26A2	1113 1312 152831 1555 1636 175 1836 231 23205 2720 2752 2923 3290 3291 3938 4051 410 4153 43 4680 5290 5291 5293 5294 5315 5743 6476 847 8809 929	Homo sapiens (human)
DOID:9778	irritable bowel syndrome Aliases: IBD Irritable colon	ACE ACHE ACSBG1 AGA AKR1B1 ARSA CAT CD14 CEACAM6 CHGA COMT CYP2B6 CYP4F3 GLB1 GLUL HSD11B1 HSD11B2 IL18R1 KLB LCT MBL2 PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PTGS2 SI SLC26A2	1113 1312 152831 1555 1636 175 1836 231 23205 2720 2752 2923 3290 3291 3938 4051 410 4153 43 4680 5290 5291 5293 5294 5315 5743 6476 847 8809 929	Homo sapiens (human)
DOID:2321	obsolete dyspepsia	AGA CD14 CHGA COMT CYP2C19 GGT1 PTGDS PTGS1 PTGS2 UGT1A9	1113 1312 1557 175 2678 54600 5730 5742 5743 929	Homo sapiens (human)
DOID:783	end stage renal disease Aliases: end stage renal failure end-stage kidney disease	ACAT1 ACE ADIPOQ CAT CHGA CPT1A CYP1A1 CYP2C8 CYP3A5 ENPP1 GHRL GLO1 ICAM1 KL LCAT LEP LIPC LPIN1 LPL MBL2 OLR1 PLA2G7 PLAUR SELL SOAT2 TLR2 TLR4 TNF UCP2	1113 1374 1543 1558 1577 1636 23175 2739 3383 38 3931 3952 3990 4023 4153 4973 5167 51738 5329 6402 7097 7099 7124 7351 7941 8435 847 9365 9370	Homo sapiens (human)
DOID:0050773	paraganglioma Aliases: chemodectoma glomus body tumor	ACACA CD44 CHGA CMAS CNTN4 DLST ENO2 FH GUSB IDH1 IDH2 MDH2 PARP1 PTEN PTGS2 SDHA SDHB SDHC SDHD SLC25A11 SMUG1 SORD TYMP VCAM1	1113 142 152330 1743 1890 2026 2271 23583 2990 31 3417 3418 4191 55907 5728 5743 6389 6390 6391 6392 6652 7412 8402 960	Homo sapiens (human)
DOID:0050757	deafness-dystonia-optic neuronopathy syndrome Aliases: Deafness Dystonia Optic Atrophy Syndrome Deafness Dystonia Optic Neuronopathy Syndrome Dystonia Deafness Syndrome Jensen syndrome Mohr-Tranebjaerg syndrome deafness dystonia syndrome	AKR1B1 CHGA MRC1 MUTYH PARP1 PIK3CA PIK3CB PIK3CD PIK3CG SDHD SLC33A1 SMUG1 TPI1	1113 142 231 23583 4360 4595 5290 5291 5293 5294 6392 7167 9197	Homo sapiens (human)
DOID:656	adrenal adenoma Aliases: adenoma of the Adrenal gland	ACACA ACADVL AKR1C3 ALOX15B CHGA CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP21A2 CYP2B6 CYP4F3 DHCR24 G6PD GAPDH HSD11B2 HSD3B2 SDHB SDHC SDHD SMUG1	1113 1555 1583 1584 1585 1586 1588 1589 1718 23583 247 2539 2597 31 3284 3291 37 4051 6390 6391 6392 8644	Homo sapiens (human)
DOID:1073	renal hypertension	ACE CHGA CYP2C8 CYP2J2 CYP3A4 CYP3A5 CYP4A11 ICAM1 SLC3A1 TM7SF2 TNF UMOD	1113 1558 1573 1576 1577 1579 1636 3383 6519 7108 7124 7369	Homo sapiens (human)
DOID:11664	nephrosclerosis Aliases: renal sclerosis	ACE ALOX5 CHGA CYP3A4 CYP3A5 CYP4A11 DCN MLYCD PTGDS SLC3A1 UMOD	1113 1576 1577 1579 1634 1636 23417 240 5730 6519 7369	Homo sapiens (human)
DOID:5394	prolactinoma Aliases: PITUITARY ADENOMA, PROLACTIN-SECRETING Prolactinoma of Pituitary gland familial prolactinoma	CHGA CNTN3 CYP19A1 GAPDH HSD17B7 KLRK1 LGALS3 MACROD1 MGAM PIK3CA PIK3CB PIK3CD PIK3CG PTGS2 QTRT1 SDHA SDHB SI	1113 1588 22914 2597 28992 3958 5067 51478 5290 5291 5293 5294 5743 6389 6390 6476 81890 8972	Homo sapiens (human)

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