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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 **1826 - 1850** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:11695	portal vein thrombosis	CHI3L1 NAAA PC PIGM SELP SLC17A5 SMUG1	1116 23583 26503 27163 5091 6403 93183	Homo sapiens (human)	DisGeNET
DOID:10230	aortic atherosclerosis Aliases: Atherosclerosis of aorta	ACE CHGA LCAT LIPG LPL PTGS2	1113 1636 3931 4023 5743 9388	Homo sapiens (human)	DisGeNET
DOID:3978	extrinsic cardiomyopathy	PFKFB3	5209	Homo sapiens (human)	DisGeNET
DOID:3951	acute myocarditis	LGALS3 LGALS9 PRKAA2 PTGS2 SMUG1 SULT1E1	23583 3958 3965 5563 5743 6783	Homo sapiens (human)	DisGeNET
DOID:11130	secondary hypertension	SLC33A1	9197	Homo sapiens (human)	DisGeNET
DOID:2889	retrocochlear disease	SUCLA2	8803	Homo sapiens (human)	DisGeNET
DOID:10964	cholesteatoma of middle ear Aliases: Cholesteatoma of middle ear and mastoid Cholesteatoma of middle ear and/or mastoid Cholesteatoma of the middle ear Epidermosis of ear Epidermosis of middle ear middle ear cholesteatoma	ICAM1 IL1R1 PSMD10 PTGS2 TLR2 TLR4 TNF TP53	3383 3554 5716 5743 7097 7099 7124 7157	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:1214	tympanosclerosis	CAT ENPP1 TLR4	5167 7099 847	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:12358	patulous eustachian tube	SCD	6319	Homo sapiens (human)	DisGeNET
DOID:14070	vestibular nystagmus Aliases: Nystagmus associated with disorder of the vestibular system	PRNP	5621	Homo sapiens (human)	DisGeNET
DOID:13789	staphyloma posticum	HADHA	3030	Homo sapiens (human)	DisGeNET
DOID:9839	accommodative esotropia	ELOVL6	79071	Homo sapiens (human)	DisGeNET
DOID:11975	coloboma of optic nerve Aliases: Coloboma of optic disc Morning glory syndrome	INPP5E PMM2	5373 56623	Homo sapiens (human)	DisGeNET
DOID:11219	conjunctival folliculosis Aliases: acute follicular conjunctivitis	PLD3	23646	Homo sapiens (human)	DisGeNET
DOID:12165	retinal lattice degeneration Aliases: Palisade degeneration of retina	RPE	6120	Homo sapiens (human)	DisGeNET
DOID:2450	central retinal vein occlusion	HPSE ICAM1 NDUFAB1 PLA2G1B PLA2G2A PLA2G6 PNP	10855 3383 4706 4860 5319 5320 8398	Homo sapiens (human)	DisGeNET
DOID:13207	proliferative diabetic retinopathy Aliases: PDR	ACE ADIPOQ AKR1A1 AKR1B1 ATP6AP2 CAT CD44 CPM DPEP1 ENO2 ENPP2 HPSE ICAM1 LGALS1 PLA2G7 PNPLA2 RBP4 RPE SDC1 SELP SORD VCAM1	10159 10327 10855 1368 1636 1800 2026 231 3383 3956 5168 57104 5950 6120 6382 6403 6652 7412 7941 847 9370 960	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	ACE ATP1A2 CAT PMM2	1636 477 5373 847	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0050835	generalized dystonia Aliases: familial dystonia fragments of torsion dystonia	ALDH5A1 ARSG CYP2U1 DBT DPEP1 ECHS1 GAD1 GCDH GLB1 GPI HIBCH MECR PDHA1 PLA2G6 SCP2 SLC39A8 SMUG1 SUCLA2	113612 1629 1800 1892 22901 23583 2571 26275 2639 2720 2821 51102 5160 6342 64116 7915 8398 8803	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:11507	rumination disorder Aliases: Psychogenic rumination	COMT FUT3 IDS	1312 2525 3423	Homo sapiens (human)	DisGeNET
DOID:11126	acquired thrombocytopenia Aliases: secondary thrombocytopenia	CRYL1	51084	Homo sapiens (human)	DisGeNET
DOID:14336	estrogen excess Aliases: hyperestrogenism	CYP19A1	1588	Homo sapiens (human)	DisGeNET
DOID:9138	stomach carcinoma in situ Aliases: carcinoma in situ of stomach gastric carcinoma in situ	MUTYH PIK3CA PIP5KL1	138429 4595 5290	Homo sapiens (human)	DisGeNET
DOID:11818	ureteric orifice cancer Aliases: Orifice of the Ureter malignant neoplasm of ureteric orifice of urinary bladder malignant tumor of ureteric orifice	DHCR24	1718	Homo sapiens (human)	DisGeNET
DOID:9460	uterine corpus cancer Aliases: corpus uteri cancer	ABO ACAT1 ACE ACSS2 ADH7 AGPAT2 AKR1B10 AKR1B1 AKR1C1 AKR1C3 ALOX5 ANXA5 APRT ATP6AP2 BAAT BST2 C1GALT1C1 CACNA2D3 CALR CAT CD44 CD55 CDH13 CEACAM5 CEACAM7 CHI3L1 CHPT1 CHST15 CHST3 COMT CSPG4 CYP11A1 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP24A1 CYP2B6 CYP2E1 CYP3A4 CYP3A7 CYP4F3 DAG1 DCN DGKA DHCR24 DHDDS DHRS11 DOLPP1 EFNA2 ENO1 ENOSF1 EXT1 FASN FH FOLR1 FOLR2 G6PC1 GALNT6 GGT1 GLO1 GOLPH3 GPC3 GPCPD1 GPI HMMR HPGDS HPSE HS3ST2 HSD17B1 HSD17B2 HSD17B4 HSD17B6 HSD17B7 HSD3B1 HSD3B2 HYAL1 HYAL2 HYAL3 IDH1 IGF2R KLRC3 L1CAM LDHA LGALS1 LGALS3 LGALS9 LPL LYPD5 MACROD1 MBD4 MBL2 MDH2 MGLL MRC1 MSLN MTAP MUTYH NCAM1 NDUFAB1 NEU1 NT5E NTHL1 OGG1 PARP1 PDIA3 PGAM2 PGK1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G15 PLA2G1B PLA2G2A PLA2G6 PLB1 PRG2 PRKAA2 PSMD10 PTEN PTGES2 PTGS2 SCD SDC1 SDHB SDHC SDHD SGPL1 SIRT2 SIRT4 SIRT6 SLC2A3 SLC2A4 SMUG1 SOAT1 SPAM1 SRD5A2 ST6GALNAC1 STS SULT1E1 SULT2B1 TNFRSF10C TNKS2 TYMP UGT1A1 UGT2B17 UGT2B7 VCAN VTCN1	1012 10159 10232 1048 10555 10855 1087 1116 11226 11343 131 1312 142 1462 1464 151056 1543 1544 1545 1551 1555 1571 1576 1583 1586 1588 1591 1604 1605 1606 1634 1636 1645 1718 1890 1943 2023 2131 2194 2271 22933 231 23409 2348 2350 23583 23659 240 2538 2678 2719 27306 2739 28 2821 284348 28992 29071 2923 308 3161 3283 3284 3292 3294 3295 3373 3417 3482 353 38 3823 3897 3939 3956 3958 3965 4023 4051 412 4153 4191 4360 4507 4595 4684 4706 4758 4907 4913 4968 51363 51478 51548 5224 5230 5290 5291 5293 5294 5315 5319 5320 54658 5553 55556 5563 55799 55808 55902 56261 56994 570 57016 5716 57171 5728 5743 6319 6382 6390 6391 6392 64083 6515 6517 6646 6677 6716 6783 6820 684 7364 7367 79154 79679 79947 80142 80351 811 8372 8398 847 8630 8644 8692 8794 8879 8930 9469 960 9956	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET

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