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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3776 - 3800** of **4621** in total

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Disease ID ▼	Disease Name	Gene Symbol	Gene ID	Organism
DOID:0080176	meningococcal meningitis	MBL2 TLR2 TLR4	4153 7097 7099	Homo sapiens (human)
DOID:0080171	esophageal atresia/tracheoesophageal fistula Aliases: esophageal atresia and/or tracheoesophageal fistula tracheoesophageal fistula with or without esohageal atresia	CEACAM5 CEACAM7	1048 1087	Homo sapiens (human)
DOID:0080169	tricuspid atresia	COMT PLD1	1312 5337	Homo sapiens (human)
DOID:0080162	lupus nephritis	ACE AGA ALG1 CALR CD38 CD44 CD74 CLEC7A CYP2B6 CYP2C19 CYP3A5 ENO1 EPHX2 EXT1 EXT2 FCGR3B FCN1 FCN2 FCN3 HPSE HSPG2 ICAM1 LGALS3 LGALS9 MBL2 OGG1 PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2R1 PTEN PTGDS PTGS1 PTGS2 SDC2 TNF VCAM1 VTCN1	10855 1555 1557 1577 1636 175 2023 2053 2131 2132 2215 2219 2220 22925 3339 3383 3958 3965 4153 4968 5236 5290 5291 5293 5294 56052 5728 5730 5742 5743 6383 64581 7124 7412 79679 811 8547 952 960 972	Homo sapiens (human)
DOID:0080161	cutaneous candidiasis	PSAP	5660	Homo sapiens (human)
DOID:0080160	Cytomegalovirus retinitis Aliases: CMV retinitis	PTGS2	5743	Homo sapiens (human)
DOID:0080159	Cryptococcal meningitis	CYP51A1 MBL2	1595 4153	Homo sapiens (human)
DOID:0080158	herpes simplex virus keratitis Aliases: dendritic keratitis	PIK3CA PIK3CB PIK3CD PIK3CG SFTPD TLR4	5290 5291 5293 5294 6441 7099	Homo sapiens (human)
DOID:0080156	X-linked adrenal hypoplasia congenita Aliases: congenital adrenal hypoplasia	AKR1B1 ALDH3A2 CHAT CYP11A1 CYP11B1 GK ICAM1 IL1RAP IL1RAPL1	1103 11141 1583 1584 224 231 2710 3383 3556	Homo sapiens (human)
DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency Aliases: VLCAD deficiency	ACADL ACADVL CHPT1 CPT1A CPT1B CPT2 LPIN1	1374 1375 1376 23175 33 37 56994	Homo sapiens (human)
DOID:0080154	short chain acyl-CoA dehydrogenase deficiency	ACADS ACADSB DLD	1738 35 36	Homo sapiens (human)
DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency	ACADM ACADS ARSA CPT1A CPT2 SLC17A5	1374 1376 26503 34 35 410	Homo sapiens (human)
DOID:0080149	adult acute monocytic leukemia	PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PRKAA2 VCAM1	5290 5291 5293 5294 5321 5563 7412	Homo sapiens (human)
DOID:0080148	T-cell childhood lymphoblastic lymphoma Aliases: Childhood T lymphoblastic lymphoma	CD33 ICAM1	3383 945	Homo sapiens (human)
DOID:0080147	lymphoblastic lymphoma	B3GAT1 CD14 CD1D CD22 CD33 CD38 CD44 CDH13 CEACAM5 CEACAM6 CEACAM7 CHST9 CLEC12A COLEC10 CSPG4 CYP1A1 CYP1A2 CYP1B1 CYP2C8 CYP2E1 CYP3A5 EBP EFNA5 ENO2 FUT4 GML HMMR HPGDS HPRT1 HS3ST4 IDH1 IDH2 IDUA IL18R1 INPP5D ISYNA1 KLRK1 LGALS1 LGALS3 LPL MBL2 MOGS MTAP NCAM1 NT5E PIGL PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PNP PNPLA3 PRKAA2 PTEN SACM1L SFTPD SMUG1 SPHK2 ST8SIA6 UGT1A1	1012 1048 10584 10682 1087 1464 1543 1544 1545 1558 1571 1577 160364 1946 2026 22908 22914 23583 2526 27087 27306 2765 3161 3251 338596 3417 3418 3425 3635 3956 3958 4023 4153 4507 4680 4684 4860 4907 51477 5290 5291 5293 5294 5305 54658 5563 56848 5728 6441 7841 80339 83539 8809 912 929 933 945 9487 952 960 9951	Homo sapiens (human)
DOID:0080146	childhood B-cell acute lymphoblastic leukemia	CD22 CD38 FCN2 FUT4 LIPA MBL2 PIK3CA PIK3CB PIK3CG SLC2A5	2220 2526 3988 4153 5290 5291 5294 6518 933 952	Homo sapiens (human)
DOID:0080145	childhood T-cell acute lymphoblastic leukemia Aliases: T-cell childhood acute lymphocytic leukemia childhood precursor T-lymphoblastic lymphoma/leukemia	ARSA CD33 FCER2 MTAP NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG POGLUT1 SULT1E1 TALDO1	2208 410 4507 4684 5290 5291 5293 5294 56983 6783 6888 945	Homo sapiens (human)
DOID:0080144	childhood acute lymphocytic leukemia Aliases: Childhood Acute Lymphoblastic Leukemia	ABO ACACA ACSS2 AKR1B1 AKR1C3 ALPI ALPP ANXA5 APRT B3GAT1 CALR CAT CD14 CD22 CD33 CD38 CD44 CD48 CD55 CD72 CEACAM6 CEL CERS6 CHI3L1 CNTFR CYP1A1 CYP1A2 CYP1B1 CYP2B6 CYP2C8 CYP2E1 CYP3A4 CYP3A5 CYP4F3 ENO2 EXT1 FADS1 FH FUT4 G6PD GAD1 GCNT2 GGT1 HK1 HPGDS HPRT1 HSD11B2 ICAM1 IDH1 IDH2 IGF2R IL18R1 IL1RL1 LIPA LSS MAN2A1 MTAP MUTYH NAAA NAMPT NCAM1 NT5E OGG1 PARP1 PARP9 PFKFB2 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PLA2G15 PNP PRKAA2 PRPS1 PTEN PTGES3 PTGS2 SELE SFTPD SHMT1 SLC27A5 SOAT1 SPHK2 SRD5A2 UGT1A6 UMOD UNG	10135 1056 10728 10998 1116 1271 142 1543 1544 1545 1555 1558 1571 1576 1577 1604 2026 2131 2271 231 23659 248 250 2526 253782 2539 2571 2651 2678 27087 27163 27306 28 308 3098 31 3251 3291 3383 3417 3418 3482 353 3988 3992 4047 4051 4124 4507 4595 4680 4684 4860 4907 4968 5208 5290 5291 5293 5294 5305 54578 5563 55902 5631 56848 5728 5743 6401 6441 6470 6646 6716 7369 7374 811 83666 847 8644 8809 9173 929 933 945 952 960 962 971	Homo sapiens (human)
DOID:0080141	mosaic variegated aneuploidy syndrome 1	CNTN3	5067	Homo sapiens (human)
DOID:0080140	multiple congenital anomalies-hypotonia-seizures syndrome 3 Aliases: M syndrome light fixation seizure syndrome	PIGT	51604	Homo sapiens (human)
DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2 Aliases: developmental and epileptic encephalopathy 20 early infantile epileptic encephalopathy 20 glycosylphosphatidylinositol biosynthesis defect 4	PIGA	5277	Homo sapiens (human)
DOID:0080138	multiple congenital anomalies-hypotonia-seizures syndrome 1	PIGN	23556	Homo sapiens (human)
DOID:0080132	Sengers syndrome Aliases: mitochondrial DNA depletion syndrome 10 mitochondrial DNA depletion syndrome 10 (cardiomyopathic type)	AGK CS	1431 55750	Homo sapiens (human)
DOID:0080128	mitochondrial DNA depletion syndrome 9 Aliases: fatal infantile lactic acidosis	SUCLA2 SUCLG1	8802 8803	Homo sapiens (human)
DOID:0080127	mitochondrial DNA depletion syndrome 8a Aliases: RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy	TYMP	1890	Homo sapiens (human)

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