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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 **2301 - 2325** of **4621** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism
DOID:8541	Sezary's disease Aliases: Sezary disease Sezary syndrome	ANXA5 CD44 IL18R1 KLRK1 MTAP PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLCG1 PTEN SDC4 SELL SOAT1	142 22914 308 4507 5290 5291 5293 5294 5335 5728 6385 6402 6646 8809 960	Homo sapiens (human)
DOID:0080188	chronic myelomonocytic leukemia	ACHE CD14 ETNK1 FCGR3B FUT4 LYZ MOGS PAFAH1B1 PARP1 SOAT1 XYLT2	142 2215 2526 4069 43 5048 55500 64132 6646 7841 929	Homo sapiens (human)
DOID:0050458	juvenile myelomonocytic leukemia	ACHE CALR CD14 CD38 ETNK1 FCGR3B FUT1 FUT4 IL18R1 IL1R1 INPP5D LYZ MOGS PAFAH1B1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SOAT1 XYLT2	142 2215 2523 2526 3554 3635 4069 43 5048 5290 5291 5293 5294 55500 5728 64132 6646 7841 811 8809 929 952	Homo sapiens (human)
DOID:4407	phototoxic dermatitis Aliases: Photosensitisation reaction Photosensitive Dermatitis Photosensitiveness	ANXA5 CAT DGAT1 FCGR3B FOLR1 INPP5K PARP1 PTGS2 RPE SMUG1 SOAT1 TMED9	142 2215 2348 23583 308 51763 54732 5743 6120 6646 847 8694	Homo sapiens (human)
DOID:0080531	dedifferentiated liposarcoma	CALR ENPP2 FASN KL PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTEN SDC1 STS	142 2194 412 5168 5290 5291 5293 5294 5716 5728 6382 811 9365	Homo sapiens (human)
DOID:0050746	mantle cell lymphoma	CD74 FASN FCER2 FH FMOD FUT1 HACD1 HPGDS MRC1 MTAP PARP1 PIK3CA PIK3CB PIK3CD PIK3CG SLC35B2 SMUG1	142 2194 2208 2271 2331 23583 2523 27306 347734 4360 4507 5290 5291 5293 5294 9200 972	Homo sapiens (human)
DOID:0050581	brachydactyly	MGAM MGAT3 PARP1 SI SLC26A2	142 1836 4248 6476 8972	Homo sapiens (human)
DOID:0050648	atelosteogenesis	ANXA5 PARP1 SLC26A2	142 1836 308	Homo sapiens (human)
DOID:1526	panniculitis	AGL PARP1 SMUG1	142 178 23583	Homo sapiens (human)
DOID:1525	nodular nonsuppurative panniculitis Aliases: Relapsing febrile nodular nonsuppurative panniculitis Weber - Christian disease Weber-Christian disease nodular non-suppurative febrile panniculitis	AGL PARP1 SMUG1	142 178 23583	Homo sapiens (human)
DOID:0060889	prune belly syndrome Aliases: Eagle-Barret syndrome Obrisnksy syndrome abdominal muscle deficiency syndrome	ACAN ALDH2 DGCR2 ICAM1 MRC1 PARP1 PTGS2 SELE SFTPD SMC3	142 176 217 3383 4360 5743 6401 6441 9126 9993	Homo sapiens (human)
DOID:12098	trigeminal neuralgia Aliases: Trifacial neuralgia trifocal neuralgia	ACLY DHCR24 PARP1 PRNP	142 1718 47 5621	Homo sapiens (human)
DOID:0060444	granular corneal dystrophy 2 Aliases: CGD2 avellino corneal dystrophy combined granular-lattice corneal dystrophy corneal dystrophy, Avellino type granular corneal dystrophy type 2	ACE CAT CD1D GCDH LPIN2 PARP1 SDC1	142 1636 2639 6382 847 912 9663	Homo sapiens (human)
DOID:10310	viral meningitis	ACE CD14 ENO2 GALNS ICAM1 LTA4H MBL2 MRC1 OGG1 PARP1 SMUG1 TPI1 VCAM1	142 1636 2026 23583 2588 3383 4048 4153 4360 4968 7167 7412 929	Homo sapiens (human)
DOID:13477	balanitis xerotica obliterans Aliases: Penile Lichen Sclerosus	DCN LIPA PARP1	142 1634 3988	Homo sapiens (human)
DOID:8616	Peyronie's disease Aliases: Induratio penis plastica Peyronie disease Peyronie's Fibromatosis	DCN LIPA PARP1	142 1634 3988	Homo sapiens (human)
DOID:0111095	Fanconi anemia complementation group A Aliases: FANCA	ALDH2 ANXA7 CAT CD33 CD44 CD48 CYP2B6 ELOVL6 FUT1 HPGDS HPRT1 ICAM1 LPL ME1 MRC1 NCAM1 NEIL1 PARP1 PFKFB3 PRKAA2 PTEN SOAT1 TIGAR VCAM1	142 1555 217 2523 27306 310 3251 3383 4023 4199 4360 4684 5209 5563 57103 5728 6646 7412 79071 79661 847 945 960 962	Homo sapiens (human)
DOID:6263	inflammatory breast carcinoma Aliases: Inflammatory carcinoma of breast Mastitis carcinomatosa	B3GAT1 CD44 CTSA CYP1B1 DHCR24 GLO1 GPX3 HAGH IDH2 INPP4B PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 SDC1 SELE	142 1545 1718 27087 2739 2878 3029 3418 5290 5291 5293 5294 5476 5728 5743 6382 6401 8821 960	Homo sapiens (human)
DOID:0050639	primary cutaneous amyloidosis Aliases: PCA familial primary localized cutaneous amyloidosis	AKR1C2 AMACR CACNA2D2 CERS2 CYP1B1 ENO2 HPGDS HSD3B1 ICAM1 IL18R1 INPP5D ISYNA1 PARP1 PKM PRNP PTEN PTGS2 SLC35A2 SRD5A1 UGT2B17 UGT2B28 XPNPEP2	142 1545 1646 2026 23600 27306 29956 3283 3383 3635 51477 5315 54490 5621 5728 5743 6715 7355 7367 7512 8809 9254	Homo sapiens (human)
DOID:11162	respiratory failure Aliases: acute and chronic respiratory failure acute respiratory Failure acute-on-chronic respiratory failure chronic respiratory failure respiratory insufficiency/failure	ABO CYP1A1 IDH1 MBL2 PARP1 PIK3C3 PTEN SFTPA2 SFTPD SLC2A10	142 1543 28 3417 4153 5289 5728 6441 729238 81031	Homo sapiens (human)
DOID:0050083	Keshan disease	ACE CYP1A1 CYP2C19 GAPDH GPX1 ICAM1 IDH2 PARP1	142 1543 1557 1636 2597 2876 3383 3418	Homo sapiens (human)
DOID:687	hepatoblastoma	ACOX2 AKR1B1 ALDOC APRT BAAT CAT CD44 CYP1A1 CYP1A2 CYP2B6 CYP3A4 CYP4F3 CYP7A1 DPEP1 G6PD GLB1 GLUL GPC3 HK1 HMGCS1 HPRT1 HSPG2 ICAM1 IL1RL1 LPIN1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PNPLA2 PPAT PSMD10 PTEN PTGS2 RGN SELENOI SLC33A1 SLC35G1 SLC37A4 SMUG1 SOAT1	142 1543 1544 1555 1576 1581 159371 1800 230 231 23175 23583 2539 2542 2719 2720 2752 3098 3157 3251 3339 3383 353 4051 5290 5291 5293 5294 5471 570 57104 5716 5728 5743 6646 8309 847 85465 9104 9173 9197 960	Homo sapiens (human)
DOID:7427	anthrax disease	CALR GALNS HACD1 LGALS1 PARP1 PLB1 STT3A	142 151056 2588 3703 3956 811 9200	Homo sapiens (human)
DOID:5688	Werner syndrome Aliases: WS Werner's syndrome adult premature ageing syndrome adult progeria	ACAN ACE ALPL APRT CAT CD55 CYP27A1 DCN ENOSF1 EXT1 FDPS G6PD GCK GGT1 GLO1 GUSB ICAM1 KL NEIL1 OGG1 PARP1 PLA2R1 PLB1 PRKAA2 PRPS1 SIRT2 SIRT6 SLC35G1	142 151056 1593 159371 1604 1634 1636 176 2131 2224 22925 22933 249 2539 2645 2678 2739 2990 3383 353 4968 51548 55556 5563 5631 79661 847 9365	Homo sapiens (human)
DOID:3911	progeria Aliases: HGPS Hutchinson Gilford syndrome Hutchinson-Gilford Progeria syndrome Hutchinson-Gilford disease	ACAN ACE ALPL APRT CAT CD55 CYP27A1 DCN ENOSF1 EXT1 FDPS G6PD GCK GGT1 GLO1 GUSB ICAM1 KL NEIL1 OGG1 PARP1 PLA2R1 PLB1 PRKAA2 PRPS1 SIRT2 SIRT6 SLC35G1	142 151056 1593 159371 1604 1634 1636 176 2131 2224 22925 22933 249 2539 2645 2678 2739 2990 3383 353 4968 51548 55556 5563 5631 79661 847 9365	Homo sapiens (human)

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