GlyCosmos Portal

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Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5826 - 5850** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism
DOID:11266	Hantavirus hemorrhagic fever with renal syndrome Aliases: HFRS Hemorrhagic fever, Russian Hemorrhagic nephrosonephritis Puumala virus nephropathy	BAAT CAT CHI3L1 ICAM2 IL1R1 IL1RL1 LGALS3 MBD4 MRC1 MUTYH NAAA PTGS1 PTGS2 SLC35D3 TM7SF2 VCAM1	1116 27163 3384 340146 3554 3958 4360 4595 570 5742 5743 7108 7412 847 8930 9173	Homo sapiens (human)
DOID:13641	exfoliation syndrome Aliases: Pseudoexfoliation glaucoma Pseudoexfoliation syndrome	CHI3L1 DPM2 GGT1 HPGDS PTEN PTGS2 TLR4	1116 2678 27306 5728 5743 7099 8818	Homo sapiens (human)
DOID:649	prion disease Aliases: Prion disease pathway Prion protein disease Spongiform Encephalopathy prion induced disorder transmissible spongiform encephalopathy	ACHE BST1 CD14 CD44 CHI3L1 GPI LGALS1 OGG1 PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 PRNP PTGS2 SMUG1	1116 23583 2821 2923 3956 43 4968 5290 5291 5293 5294 5563 5621 5743 683 929 960	Homo sapiens (human)
DOID:11695	portal vein thrombosis	CHI3L1 NAAA PC PIGM SELP SLC17A5 SMUG1	1116 23583 26503 27163 5091 6403 93183	Homo sapiens (human)
DOID:12556	acute kidney tubular necrosis Aliases: ATN - acute tubular necrosis acute renal Failure with tubular necrosis acute renal failure with lesion of tubular necrosis acute tubular necrosis acute tubule necrosis	ARSA ARSD CHI3L1 MLYCD PTGS2	1116 23417 410 414 5743	Homo sapiens (human)
DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma Aliases: cutaneous T cell lymphoma cutaneous T-cell lymphoma	ANXA5 CD22 CD44 CHI3L1 CNTN2 LGALS1 LGALS9 MBL2 MTAP NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLCG1 PTEN PTGS2 SDC4 SELL SIRT2 SOAT1 TIGAR	1116 22933 308 3956 3965 4153 4507 4684 5290 5291 5293 5294 5315 5335 57103 5728 5743 6385 6402 6646 6900 933 960	Homo sapiens (human)
DOID:0080544	hyper IgM syndrome Aliases: HIGM hyperimmunoglobulin M syndrome immunodeficiency with hyper-IgM	CHI3L1 FCER2 MRC1 UNG	1116 2208 4360 7374	Homo sapiens (human)
DOID:6620	X-linked hyper IgM syndrome Aliases: HIGM1 X-linked hyper-IgM immunodeficiency XHIM hyper-IgM immunodeficiency syndrome type 1 hyper-IgM syndrome 1 hyper-IgM syndrome type 1 immunodeficiency with hyper-IgM type 1	CHI3L1 FCER2 MRC1 UNG	1116 2208 4360 7374	Homo sapiens (human)
DOID:0060023	immunodeficiency with hyper IgM type 3 Aliases: CD40 deficiency HIGM3 hyper-IgM syndrome due to CD40 deficiency type 3 hyper-IgM immunodeficiency	CHI3L1 FCER2 MRC1 UNG	1116 2208 4360 7374	Homo sapiens (human)
DOID:0060022	CD40 ligand deficiency Aliases: HIGMX-1 X-linked hyper-IgM syndrome	CHI3L1 FCER2 HPRT1 IL18R1 MRC1 PIK3CA PIK3CB PIK3CD PIK3CG UNG	1116 2208 3251 4360 5290 5291 5293 5294 7374 8809	Homo sapiens (human)
DOID:10533	viral pneumonia	ACE CHI3L1	1116 1636	Homo sapiens (human)
DOID:14069	cerebral malaria Aliases: Malarial encephalitis	ACE ALOX5 CAT CHI3L1 ENOSF1 FH ICAM1 IL1R1 ISYNA1 LGALS2 MBL2 MPPE1 PNP PRKAA2 PTGS2 SELE	1116 1636 2271 240 3383 3554 3957 4153 4860 51477 55556 5563 5743 6401 65258 847	Homo sapiens (human)
DOID:0111275	speech-language disorder-1 Aliases: CAS articulatory apraxia childhood apraxia of speech developmental apraxia of speech developmental verbal dyspraxia speech and language disorder with orofacial dyspraxia speech-language disorder type 1	ACE ALDH2 B3GAT1 CHI3L1 FASN FCGR3B GALT LGALS1	1116 1636 217 2194 2215 2592 27087 3956	Homo sapiens (human)
DOID:11650	bronchopulmonary dysplasia Aliases: Bronchopulmonary dysplasia of newborn Chronic lung disease of prematurity Neonatal chronic lung disease Perinatal bronchopulmonary dysplasia Respiratory insufficiency neonatal chronic respiratory disease	CAT CD209 CHI3L1 DAG1 MBL2 SFTPA1 SFTPD TNF TP53	1116 1605 30835 4153 6441 653509 7124 7157 847	Homo sapiens (human)
DOID:11722	myotonic dystrophy type 1 Aliases: Dystrophia myotonica Steinert disease congenital myotonic dystrophy myotonic dystrophy of Steinert	ACE ALPP ATRNL1 CAT CHI3L1 CYP2B6 DAG1 DGCR2 FASN GAD2 GCK HAS2 HSPG2 LPL MGAM MRC1 MTM1 MTMR1 PGD PGP PLCB1 PRKAA2 PRNP SELE SELP SI SIRT6 SLC2A4 SLC35G1 ST8SIA4 UGT8	1116 1555 159371 1605 1636 2194 23236 250 2572 26033 2645 283871 3037 3339 4023 4360 4534 51548 5226 5563 5621 6401 6403 6476 6517 7368 7903 847 8776 8972 9993	Homo sapiens (human)
DOID:0110227	cataract 32 multiple types Aliases: CTRCT32	ACE AGK ALDH7A1 CHI3L1 CRYL1 CYP1A1 CYP27A1 FCGR3B FCN2 GALK1 GCNT2 GPC5 INPP5K LSS MBL2 OCRL PTEN SDC4 SFTPA1 SFTPA2 SFTPD SLC17A5 SLC2A10 SLC33A1 SMC3 SMPD1 SORD	1116 1543 1593 1636 2215 2220 2262 2584 26503 2651 4047 4153 4952 501 51084 51763 55750 5728 6385 6441 653509 6609 6652 729238 81031 9126 9197	Homo sapiens (human)
DOID:6132	bronchitis Aliases: CI - Chest infection Chest infection acute Bronchitis chest cold chronic bronchitis recurrent wheezy bronchitis	CHI3L1 CHID1 CYP1A1 CYP2B6 HPGDS ICAM1 MBL2 PLA2G6 PTGDS SFTPD	1116 1543 1555 27306 3383 4153 5730 6441 66005 8398	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:9368	keratoconjunctivitis	ALOX12B ARSA CAT CD38 CERS3 CHI3L1 CLEC4E CLEC7A OLR1 PLA2G1B PLA2G2A PLA2G6 PLB1 PLD3 SIRT6 TLR2	1116 151056 204219 23646 242 26253 410 4973 51548 5319 5320 64581 7097 8398 847 952	Homo sapiens (human)
DOID:4677	keratitis	ALOX12B ARSA CAT CD38 CERS3 CHI3L1 CLEC4E CLEC7A OLR1 PLA2G1B PLA2G2A PLA2G6 PLB1 PLD3 SIRT6 TLR2 TLR4	1116 151056 204219 23646 242 26253 410 4973 51548 5319 5320 64581 7097 7099 8398 847 952	Homo sapiens (human)
DOID:1584	acute chest syndrome Aliases: acute chest syndrome in sickle cell disease	ABO ACACA ACACB ACE ACSL5 ACSL6 ACSS2 ALDH2 ALOX5 ARSA CD14 CD44 CHI3L1 CYP1A1 CYP2C19 CYP3A4 CYP3A5 ELOVL2 EPHX2 FADS1 FASN FCGR3B G6PD GALNT4 GCK HYAL2 ICAM1 L1CAM LCAT LGALS3 LIPA LIPG LPL OGG1 OLR1 PCYT1A PLA2G15 PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLB1 PLCB4 PTGS1 PTGS2 SELE SELL SELP SLC39A8 SMUG1 VCAM1	1116 151056 1543 1557 1576 1577 1636 2053 217 2194 2215 23305 23583 23659 240 2539 2645 28 31 32 3383 3897 3931 3958 3988 3992 4023 410 4968 4973 5130 51703 5320 5321 5332 54898 55902 5742 5743 6401 6402 6403 64116 7412 7941 8398 8692 8693 929 9388 960	Homo sapiens (human)
DOID:2378	relapsing-remitting multiple sclerosis Aliases: RRMS Relapsing-remitting MS	CD14 CHI3L1 CSPG4 CYP24A1 DHCR24 HPRT1 ICAM1 KL PLD1 RTN4R SDC1 VCAM1	1116 1464 1591 1718 3251 3383 5337 6382 65078 7412 929 9365	Homo sapiens (human)
DOID:2799	bronchiolitis obliterans Aliases: Bronchiolitis exudativa Bronchiolitis fibrosa obliterans Obliterative bronchiolitis	ACE CHI3L1 ICAM1 KLRK1 MBL2 PIK3CD SELE SFTPA1 SFTPD VCAN	1116 1462 1636 22914 3383 4153 5293 6401 6441 653509	Homo sapiens (human)
DOID:2800	acute interstitial pneumonia Aliases: AIP Hamman-Rich disease Hamman-Rich syndrome Idiopathic pulmonary fibrosis, acute fatal form accelerated interstitial pneumonia acute interstitial pneumonitis	AMY2A ARSA CHI3L1 DCN DEGS1 ENO1 MBL2 PKD1 PTEN PTGS2 RECK SDC4 SFTPA1 SFTPA2 SFTPC SFTPD SMUG1 VCAN	1116 1462 1634 2023 23583 279 410 4153 5310 5728 5743 6385 6440 6441 653509 729238 8434 8560	Homo sapiens (human)
DOID:3669	intermittent claudication Aliases: Charcot's syndrome	ABO ACE AGXT ALDH7A1 BAD CALR CD14 CHI3L1 CYP1A1 CYP1A2 CYP2C19 DLD ENPP1 GPX1 ICAM1 KLRB1 LIPC PCYT1A SIRT2 SLC2A10 SRD5A1 VCAM1 VCAN XYLT1 XYLT2	1116 1462 1543 1544 1557 1636 1738 189 22933 28 2876 3383 3820 3990 501 5130 5167 572 64131 64132 6715 7412 81031 811 929	Homo sapiens (human)

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