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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 **851 - 875** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:3846	adamantinous craniopharyngioma Aliases: Adamantinous Rathke's Pouch tumor craniopharyngioma, adamantinomatous	ATP6AP2 CD44 CEL CYP2E1 GAD1 GPX1 HSD11B1 IDH1 LGALS1 NDUFAB1	10159 1056 1571 2571 2876 3290 3417 3956 4706 960	Homo sapiens (human)
DOID:3840	craniopharyngioma Aliases: neoplasm of Rathke's Pouch	ATP6AP2 CD44 CEL CYP2E1 GAD1 GPX1 HSD11B1 IDH1 LGALS1 NDUFAB1	10159 1056 1571 2571 2876 3290 3417 3956 4706 960	Homo sapiens (human)
DOID:1712	aortic valve stenosis Aliases: Aortic stenosis Rheumatic aortic stenosis rheumatic aortic valve stenosis	ACAN ACE ALOX5 ARSD ATP6AP2 ATP6V0A2 B3GALT6 B3GAT3 B4GALT7 CD14 CD44 CHST3 CTSA CYP11B2 CYP24A1 EBP ENO3 ENPP1 FCGR3B FH GAPDH GLB1 GNPTG ICAM1 IDUA KL LGALS3 LGALS4 MPG NT5E OGA OGT PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 PLPP3 PSAP PTDSS1 SDC1 SDC4 SLC2A10 STS TNF	10159 10682 10724 11285 126792 1585 1591 1636 176 2027 2215 2271 23545 240 2597 26229 2720 3383 3425 3958 3960 412 414 4350 4907 5167 5290 5291 5293 5294 5476 5660 6382 6385 7124 7941 81031 84572 8473 8613 929 9365 9469 960 9791	Homo sapiens (human)
DOID:0080334	aortic valve disease 2	ACAN ACE ALOX5 ARSD ATP6AP2 ATP6V0A2 B3GALT6 B3GAT3 B4GALT7 CD14 CHST3 CTSA CYP11B2 CYP24A1 EBP ENO3 ENPP1 FCGR3B FH GAPDH GLB1 GNPTG IDUA LGALS3 LGALS4 MPG NT5E OGA OGT PIK3CA PIK3CB PIK3CD PIK3CG PSAP PTDSS1 SDC1 SDC4 SLC2A10 STS	10159 10682 10724 11285 126792 1585 1591 1636 176 2027 2215 2271 23545 240 2597 26229 2720 3425 3958 3960 412 414 4350 4907 5167 5290 5291 5293 5294 5476 5660 6382 6385 81031 84572 8473 929 9469 9791	Homo sapiens (human)
DOID:13548	secondary Parkinson disease Aliases: Symptomatic parkinsonism disorder presenting primarily with parkinsonism secondary parkinsonism	ABAT ACHE ADH1C AKR1C4 ATP6AP2 CHAT COMT CYP19A1 CYP1A2 CYP27A1 DPEP1 ENO2 GAD2 GBA1 GFRA1 GFRA2 GLB1 GLUL HPGDS LGALS1 MAG MYORG OGA PAFAH1B1 PARP1 PLA2G6 PLB1 PPT1 PRNP PTEN PTGS2 SIRT2 SMUG1 ST8SIA1 SYNJ1	10159 10724 1103 1109 126 1312 142 151056 1544 1588 1593 18 1800 2026 22933 23583 2572 2629 2674 2675 2720 27306 2752 3956 4099 43 5048 5538 5621 5728 5743 57462 6489 8398 8867	Homo sapiens (human)
DOID:13068	renal osteodystrophy Aliases: renal rickets	ACE ACLY ATP6AP2 CD44 DLST FASN FH GPX1 ICAM1 ISYNA1 KL LCAT MBL2 MDH2 NAGLU NT5E OGA OLR1 PTGS2 SDHA SDHB SDHC SDHD ST3GAL4 VCAN VNN1	10159 10724 1462 1636 1743 2194 2271 2876 3383 3931 4153 4191 4669 47 4907 4973 51477 5743 6389 6390 6391 6392 6484 8876 9365 960	Homo sapiens (human)
DOID:11713	diabetic angiopathy Aliases: Diabetic vascular disorder diabetic peripheral angiopathy	ACE AKR1B1 ATP6AP2 CANX CAT GPX1 HPSE ICAM1 LGALS3 PTEN RBP4 RENBP SELL SMPD1 TNF	10159 10855 1636 231 2876 3383 3958 5728 5950 5973 6402 6609 7124 821 847	Homo sapiens (human)
DOID:10591	pre-eclampsia Aliases: gestational hypertension hypertension induced by pregnancy pre-eclamptic toxaemia preeclampsia preeclampsia/eclampsia pregnancy associated hypertension pregnancy toxemia proteinuric hypertension of pregnancy toxaemia of pregnancy	ACE ACOT7 AKR1C3 ANXA5 ATP6AP2 CALR CHI3L1 COMT CYP11B1 CYP11B2 CYP19A1 CYP21A2 CYP24A1 CYP27B1 CYP2J2 CYP2R1 CYP3A5 EFNA1 ENPP1 GAPDH GPI GPX1 GPX3 HADHA HPGDS HSD11B1 HSD11B2 HSD3B1 HSD3B2 HSPG2 ICAM1 IL18R1 ISYNA1 LEP LEPR LGALS1 LIPC LPL MBL2 OGG1 OLR1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLA2G6 PLAUR PLB1 PTGDS PTGS1 PTGS2 PYGM RBP4 RENBP SDC1 SELL SIRT4 SLC17A5 SLC2A1 TLR4 TNF VCAM1	10159 1116 11332 120227 1312 151056 1573 1577 1584 1585 1588 1589 1591 1594 1636 1942 23409 2597 26503 27306 2821 2876 2878 3030 308 3283 3284 3290 3291 3339 3383 3952 3953 3956 3990 4023 4153 4968 4973 51477 5167 5290 5291 5293 5294 5320 5329 5730 5742 5743 5837 5950 5973 6382 6402 6513 7099 7124 7412 811 8398 8644 8809	Homo sapiens (human)
DOID:1681	heart septal defect Aliases: Cardiac septal defects Congenital septal defect of heart septal defect	ALG8 ALG9 ATP6AP2 B3GALT6 B3GLCT DAG1 NSDHL PIGN	10159 126792 145173 1605 23556 50814 79053 79796	Homo sapiens (human)
DOID:13593	eclampsia Aliases: Eclampsia in puerperium Eclampsia, postpartum Postpartum eclampsia	ABO ACE ADH5 ANXA5 ATP6AP2 CALR CD14 COMT CYP11B2 CYP2C9 DGKI HSD11B2 IL18R1 KLRB1 LPL MBL2 PTGS1 PTGS2 SORD	10159 128 1312 1559 1585 1636 28 308 3291 3820 4023 4153 5742 5743 6652 811 8809 9162 929	Homo sapiens (human)
DOID:4188	echolalia	ATP6AP2 HGSNAT SLC35C1	10159 138050 55343	Homo sapiens (human)
DOID:2725	capillary hemangioma Aliases: Capillary haemangioma Congenital vascular hamartoma Congenital vascular naevus Infantile hemangioma Juvenile hemangioma Strawberry haemangioma Strawberry nevus Strawberry nevus of skin cellular hemangioma of Infancy	ACE ATP6AP2 ATP6V1A C1GALT1C1 CYP1B1 GNPTAB MAG MTM1 MTMR14 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SDHC SDHD SRD5A3	10159 1545 1636 29071 4099 4534 523 5290 5291 5293 5294 5728 6391 6392 64419 79158 79644	Homo sapiens (human)
DOID:12935	alcoholic cardiomyopathy Aliases: Alcohol-induced heart muscle disease Dilated cardiomyopathy secondary to alcohol	ACE ALDH2 ATP6AP2 CYP2E1 GAPDH	10159 1571 1636 217 2597	Homo sapiens (human)
DOID:446	primary hyperaldosteronism Aliases: Cushing syndrome Cushing's syndrome hyperaldosteronism	ACAT1 ACE AKR1B1 APRT ATP6AP2 CD44 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP21A2 CYP3A4 CYP4F3 FASN FH G6PD HSD11B1 HSD11B2 HSD3B1 HSD3B2 LGALS3 OCRL PRSS8 PTGS2 SLC26A2 SLC33A1 SLC5A1 SMUG1	10159 1576 1583 1584 1585 1586 1588 1589 1636 1836 2194 2271 231 23583 2539 3283 3284 3290 3291 353 38 3958 4051 4952 5652 5743 6523 9197 9469 960	Homo sapiens (human)
DOID:445	Bartter disease Aliases: Aldosteronism with hyperplasia of the adrenal cortex Bartter's syndrome	ATP6AP2 CD44 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP21A2 CYP4F3 G6PD HSD11B2 HSD3B1 HSD3B2 LGALS3 OCRL PRSS8 PTGS2 SLC26A2 SLC33A1 SLC5A1	10159 1583 1584 1585 1586 1589 1836 2539 3283 3284 3291 3958 4051 4952 5652 5743 6523 9197 9469 960	Homo sapiens (human)
DOID:12028	Conn's syndrome Aliases: Conn syndrome primary aldosteronism	ATP6AP2 CD44 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP21A2 CYP4F3 G6PD HSD11B2 HSD3B1 HSD3B2 LGALS3 OCRL PRSS8 PTGS2 SLC26A2 SLC33A1 SLC5A1	10159 1583 1584 1585 1586 1589 1836 2539 3283 3284 3291 3958 4051 4952 5652 5743 6523 9197 9469 960	Homo sapiens (human)
DOID:9931	Waterhouse-Friderichsen syndrome Aliases: Meningococcal hemorrhagic adrenalitis	ATP6AP2 CD44 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP21A2 CYP4F3 G6PD HSD11B2 HSD3B1 HSD3B2 LGALS3 OCRL PRSS8 SLC26A2 SLC33A1 SLC5A1	10159 1583 1584 1585 1586 1589 1836 2539 3283 3284 3291 3958 4051 4952 5652 6523 9197 9469 960	Homo sapiens (human)
DOID:0080205	CAKUT Aliases: Congenital anomalies of the kidney and urinary tract Renal or urinary tract malformation	ACE ATP6AP2 FREM1 PIK3CA PIK3CB PIK3CD PIK3CG	10159 158326 1636 5290 5291 5293 5294	Homo sapiens (human)
DOID:4028	angioma serpiginosum Aliases: Angioma serpiginosum of skin	ACE ATP6AP2 ATP6V1A C1GALT1C1 MAG PIK3CA PIK3CB PIK3CD PIK3CG PTEN SRD5A3	10159 1636 29071 4099 523 5290 5291 5293 5294 5728 79644	Homo sapiens (human)
DOID:2411	granular cell tumor Aliases: neoplasm of granular cell	ATP6AP2 FASN PTEN	10159 2194 5728	Homo sapiens (human)
DOID:2942	bronchiolitis	ATP6AP2 CD14 CD38 FUT2 ICAM1 IL1RL1 ISYNA1 KLRK1 MBL2 PLCG2 PTGDS SFTPA1 SFTPD	10159 22914 2524 3383 4153 51477 5336 5730 6441 653509 9173 929 952	Homo sapiens (human)
DOID:12387	nephrogenic diabetes insipidus	ATP6AP2 CANX G6PD L1CAM PRKAA2 PTGS2	10159 2539 3897 5563 5743 821	Homo sapiens (human)
DOID:0060135	apraxia	ATP6AP2 COG4 EPM2A GCK GPAA1 PRNP	10159 25839 2645 5621 7957 8733	Homo sapiens (human)
DOID:12385	shigellosis Aliases: Shigella boydii infectious disease Shigella flexneri infectious disease Shigella gastroenteritis Shigella sonnei infectious disease bacillary dysentery	ATP6AP2 BCKDHA CD248 CD48 CLEC7A CTSA GUSB HSD17B6 LYZ SFTPA1 ST8SIA2	10159 2990 4069 5476 57124 593 64581 653509 8128 8630 962	Homo sapiens (human)
DOID:0060309	syndromic X-linked intellectual disability Aliases: syndromic X-linked mental retardation	ATP6AP2	10159	Homo sapiens (human)

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