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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 **4751 - 4775** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:0080630	B-lymphoblastic leukemia/lymphoma Aliases: B lymphoblastic leukemia/lymphoma B-ALL precursor B lymphoblastic lymphoma/leukemia	AKR1C3 CYP3A5 TP53	1577 7157 8644	Homo sapiens (human)	Alliance of Genome Resources
DOID:3213	demyelinating disease Aliases: demyelinating disorder	ARSA CD1D FIG4 GALC GPC5 HPRT1 ICAM1 KL LGALS3 MAG PTGS2	2262 2581 3251 3383 3958 4099 410 5743 912 9365 9896	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:2557	chondromalacia	ACAN IL1R1	176 3554	Homo sapiens (human)	DisGeNET DisGeNET
DOID:1143	exotropia Aliases: Divergent Strabismus Divergent concomitant strabismus	ACADSB DPAGT1 HADHA NGLY1 PIGQ PRPS1 SLC17A5 SLC35A2	1798 26503 3030 36 55768 5631 7355 9091	Homo sapiens (human)	DisGeNET
DOID:3159	photosensitivity disease Aliases: Photodermatitis	DHCR7 EPM2A FDPS KDSR PTGS2	1717 2224 2531 5743 7957	Homo sapiens (human)	DisGeNET DisGeNET
DOID:731	urinary system benign neoplasm Aliases: neoplasm of urinary system tumor of the urinary system tumor of urinary tract urinary tract neoplasm	ACE ACSS2 CEACAM5 CEACAM7 COMT OGG1 PIK3CA PLA2G15	1048 1087 1312 1636 23659 4968 5290 55902	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11256	typhus Aliases: Endemic Typhus fever Exanthematic Typhus fever Flea typhus Louse-borne [epidemic] typhus Moscow typhus Murine [endemic] typhus Typhus fever endemic flea-borne typhus epidemic louse-borne typhus	ACHE ALPI ALPP APRT CS DHCR24 LSS MTAP PTGS2 SMUG1	1431 1718 23583 248 250 353 4047 43 4507 5743	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:2316	brain ischemia Aliases: Ischaemic encephalopathy Ischemic encephalopathy cerebral ischemia	ACE AKT1 ALOX15 ALOX5 APEX1 BAD CAT CSPG4 CYP19A1 ENO2 FCN1 G6PD GCDH GFRA1 GPNMB GPX1 ICAM1 IL6ST LGALS1 LGALS3 MBL2 MDH2 NAMPT PARP1 PCNA PGP PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PMM2 PRNP PTGIS PTGS1 PTGS2 SELE SLC33A1 TLR4	10135 10457 142 1464 1588 1636 2026 207 2219 240 246 2539 2639 2674 283871 2876 328 3383 3572 3956 3958 4153 4191 5111 5290 5291 5293 5294 5321 5373 5621 572 5740 5742 5743 6401 7099 847 9197	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:9682	yellow fever Aliases: Sylvatic yellow fever Yellow fever, sylvan jungle yellow fever urban yellow fever	ABO ACHE AGPAT1 AMACR ANXA5 APRT BST2 CAT CD14 CD209 CD33 CD38 CERS1 CHST10 CLEC5A CSPG5 DDOST FASN FCGR3B G6PD GAPDH GOLPH3 HPSE2 HPSE HSD17B6 ICAM1 IL1RL1 KLRC1 LGALS9 MBL2 MGAM MICA MOGS MRC1 NAAA PIK3CA PIK3CB PIK3CD PIK3CG PLCE1 PRKAA2 PRNP PTGS2 SCD SELE SI SIRT6 SLC17A5 SMUG1 SOAT1 SPHK1 SPHK2 STT3B TM7SF2 TPI1 VCAM1	100507436 10554 10675 10715 10855 1650 201595 2194 2215 23583 23600 23601 2539 2597 26503 27163 28 308 30835 3383 353 3821 3965 4153 43 4360 51196 51548 5290 5291 5293 5294 5563 5621 56848 5743 60495 6319 6401 64083 6476 6646 684 7108 7167 7412 7841 847 8630 8877 8972 9173 929 945 9486 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0111029	hemochromatosis type 1 Aliases: HFE1 symptomatic form of HFE-related hereditary hemochromatosis symptomatic form of classic hemochromatosis symptomatic form of hemochromatosis type 1	ACO1 AKR1B1 AKR1D1 ALDH2 CALR CD14 FADS2 FUT1 FUT2 GNPAT GPC1 GPC3 GPC5 HJV HPGDS ICAM1 LGALS3 PIK3CA PIK3CB PIK3CD PIK3CG PNPLA3 SELE SELL STS SULT1E1 TUSC3 UGT1A1 VCAM1	148738 217 2262 231 2523 2524 2719 27306 2817 3383 3958 412 48 5290 5291 5293 5294 54658 6401 6402 6718 6783 7412 7991 80339 811 8443 929 9415	Homo sapiens (human)	DisGeNET DisGeNET
DOID:9975	cocaine dependence	ABAT COMT EXTL3 FDFT1 GAD1 GAD2 HTR2A MANEA MDH2 NTNG1 PER2 PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 RECK SIRT2 SMUG1 UMOD	1312 18 2137 2222 22854 22933 23583 2571 2572 3356 4191 5290 5291 5293 5294 5563 7369 79694 8434 8864	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:5608	dental pulp calcification Aliases: pulp calcification pulp calcifications pulpal calcifications	GALNT3	2591	Homo sapiens (human)	DisGeNET
DOID:7428	pineal region germinoma	CALR	811	Homo sapiens (human)	DisGeNET
DOID:14256	adult-onset Still's disease Aliases: adult onset Still's disease adult-onset Still disease	CLEC7A GCK ICAM1 SELL SMUG1	23583 2645 3383 6402 64581	Homo sapiens (human)	DisGeNET
DOID:9477	pulmonary embolism Aliases: pulmonary artery embolism pulmonary embolus	ABO ACE CAT CD55 CHGA DPEP1 EXTL3 PCYT1A PIGA PTEN QTRT1 SELE SELP SIRT2 TBXAS1 VCAM1	1113 1604 1636 1800 2137 22933 28 5130 5277 5728 6401 6403 6916 7412 81890 847	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:5884	benign intermediate mesothelioma Aliases: Well-differentiated Papillary tumor of Mesothelium	L1CAM	3897	Homo sapiens (human)	DisGeNET
DOID:11328	schizophreniform disorder	ACADS ACHE ACOT7 ACSL6 ADH1B AGA ALDH2 ALDH5A1 ALG9 ARSA ARSB B3GAT1 CALR CHI3L1 CHPT1 COMT CYP27B1 CYP2B6 DHDDS EPM2A G6PD GAD1 GAD2 GLUL HPGDS LGALS3 ME2 MGAT1 NPL PAFAH1B1 PIK3C2A PLA2G1B PLA2G4A PLCB4 PPT1 PRNP RPN2 RTN4R SLC27A5 SMUG1 SPTLC1 ST3GAL1 UXS1 VCAM1	10558 10998 1116 11332 125 1312 1555 1594 175 217 23305 23583 2539 2571 2572 27087 27306 2752 35 3958 410 411 4200 4245 43 5048 5286 5319 5321 5332 5538 5621 56994 6185 6482 65078 7412 7915 7957 79796 79947 80146 80896 811	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:12351	alcoholic hepatitis Aliases: acute alcoholic hepatitis acute alcoholic liver disease	ACE ADH1A ADH1B ADH1C ADH4 AGA AKR1A1 AKR1B1 ALDH1B1 ALDH2 CD14 CD74 CEACAM5 CERS6 CHST3 CPT1A CYP1A1 CYP2E1 CYP7A1 FUT1 GAPDH HK2 HPGDS HSPG2 ICAM1 IL18R1 IL1R1 MBOAT7 MRC1 NAMPT NCAN PIK3CA PIK3CB PIK3CD PIK3CG PNPLA3 PPARA PRNP SIRT6 SLC17A5 SMPD1 SPHK2 ST6GAL1 ST8SIA4 STS SULT1E1 TBXAS1 TNF	10135 10327 1048 124 125 126 127 1374 1463 1543 1571 1581 1636 175 217 219 231 2523 253782 2597 26503 27306 3099 3339 3383 3554 412 4360 51548 5290 5291 5293 5294 5465 5621 56848 6480 6609 6783 6916 7124 7903 79143 80339 8809 929 9469 972	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2510	Kluver-Bucy syndrome Aliases: Klver-Bucy syndrome	NAGLU SGSH	4669 6448	Homo sapiens (human)	DisGeNET
DOID:0111060	Ambras type hypertrichosis universalis congenita Aliases: Ambras syndrome HTC1	EFNA5	1946	Homo sapiens (human)	DisGeNET
DOID:1116	pertussis Aliases: WC - Whooping cough bordetella infection whooping cough	ACOT7 PIK3CG UMOD	11332 5294 7369	Homo sapiens (human)	DisGeNET
DOID:2018	hyperinsulinism Aliases: hyperinsulinemia	ACACA ACE ACLY ADIPOQ AGPAT2 AKR1C3 ALDH2 AMY1A AMY1B AMY1C CA4 CANX CD14 CPT1A CRYL1 CS CYP17A1 CYP19A1 CYP1A2 DHDDS EHHADH ELOVL6 ENPP1 FASN FCGR3B FCN2 G6PC1 G6PC2 GCK GFPT1 GLA GLB1 GPX1 H6PD HADH HGSNAT HK2 HPGDS HSD11B1 IDH3A IDH3B INS KCNJ11 KL LEP LEPR LIPC LPIN1 LPL MELTF MGAT5 MPI NEIL1 OGT PDHX PFKFB1 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PMM2 PNPLA2 PNPLA3 POMGNT1 PRKAA2 PTEN PTGDS RBP4 RENBP SCD SFTPA1 SFTPA2 SFTPC SIGLEC7 SIRT4 SLC2A3 SLC2A4 ST3GAL4 TM7SF2 UGDH UGT1A1 VCAM1	10555 1374 138050 1431 1544 1586 1588 1636 1962 217 2194 2215 2220 23175 23409 2538 2645 2673 27036 2717 2720 27306 276 277 278 2876 3033 3099 31 3290 3419 3420 3630 3767 3952 3953 3990 4023 4241 4249 4351 47 51084 5167 5207 5290 5291 5293 5294 5310 5373 54658 55624 5563 57104 5728 5730 57818 5950 5973 6319 6440 6484 6515 6517 653509 7108 729238 7358 7412 762 79071 79661 79947 80339 8050 821 8473 8644 929 9365 9370 9563	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0111910	spermatogenic failure Aliases: SPGF	PDHA2	5161	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060409	NFIA-related disorder Aliases: 1p31p32 microdeletion syndrome Chromosome 1, Monosomy 1p32 brain malformations with or without urinary tract defects chromosome 1p32-p31 deletion syndrome	CYP11A1 FREM1 PAFAH1B1 PRNP	1583 158326 5048 5621	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0050462	Antley-Bixler syndrome with disordered steroidogenesis Aliases: trapezoidocephaly-synostosis syndrome	CYP1A2 CYP2B6 CYP51A1	1544 1555 1595	Homo sapiens (human)	DisGeNET DisGeNET

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