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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4376 - 4400** of **5716** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0050152	aspiration pneumonia	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:12549	hepatitis A Aliases: Viral hepatitis, type A	ACE XRCC1	1636 7515	Homo sapiens (human)	Alliance of Genome Resources
DOID:3500	gallbladder adenocarcinoma Aliases: adenocarcinoma of the gallbladder	ACE DDR2	1636 4921	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080599	Coronavirus infectious disease	ACE CD209 MBL2	1636 30835 4153	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050864	non-arteritic anterior ischemic optic neuropathy Aliases: non-arteritic anterior ischaemic optic neuropathy nonarteritic anterior ischaemic optic neuropathy nonarteritic anterior ischemic optic neuropathy	ACE F5 GP1BA ITGB3	1636 2153 2811 3690	Homo sapiens (human)	Alliance of Genome Resources
DOID:2355	anemia Aliases: anaemia	ACE ANK1 EPOR G6PD GPX1 HK1 PON1 SLC11A2 TF	1636 2057 2539 286 2876 3098 4891 5444 7018	Homo sapiens (human)	Alliance of Genome Resources
DOID:8432	polycythemia Aliases: Erythrocythemia	ACE EPAS1 EPOR HBB	1636 2034 2057 3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080600	COVID-19 Aliases: 2019 Novel Coronavirus (2019-nCoV) 2019-nCoV infection COVID19 SARS-CoV-2 infection Wuhan coronavirus infection Wuhan seafood market pneumonia virus infection	A2M ABO ACE2 ACE AGTR1 C3 C4BPA C4BPB CFH F3 HLA-B HLA-C IFNB1 IFNL1 KIR3DS1 PLG SERPINF2 SERPING1 TLR7	1636 185 2 2152 28 282618 3075 3106 3107 3456 3813 51284 5340 5345 59272 710 718 722 725	Homo sapiens (human)	Alliance of Genome Resources
DOID:11123	IgA vasculitis Aliases: Allergic purpura Autoimmune purpura HSP Henoch Schoenlein purpura Henoch Scholein purpura Henoch Schonlein purpura Henoch Schönlein purpura Henoch-Schoenlein purpura Henoch-Scholein purpura Henoch-Schonlein purpura Henoch-Schönlein purpura IgAV Purpura, autoimmune immunoglobulin A vasculitis	ACE AGT CCL2 CD86 HLA-DQA1 IL1RN MEFV PON1	1636 183 3117 3557 4210 5444 6347 942	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060224	atrial fibrillation Aliases: A-fib AFib	ACE AGT ANK2 KCNE1 KCNE2 KCNJ5 KCNQ1 MMP1 MMP3 VWF	1636 183 287 3753 3762 3784 4312 4314 7450 9992	Homo sapiens (human)	Alliance of Genome Resources
DOID:14499	Fabry disease Aliases: Alpha-galactosidase A deficiency Angiokeratoma Corporis Diffusum Fabry Disease, Cardiac Variant Fabry's disease alpha galactosidase deficiency deficiency of melibiase	ACE AGT GLA IL1A	1636 183 2717 3552	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:988	mitral valve prolapse Aliases: Barlow's syndrome floppy mitral valve	ACE AGT DCHS1 DZIP1 FBN1 FLNA HLA-B PLAU TSHR	1636 183 2200 22873 2316 3106 5328 7253 8642	Homo sapiens (human)	Alliance of Genome Resources
DOID:576	proteinuria	ACE AGER IL1RN MYH9 PLA2G7 SNRPD1 TLR9	1636 177 3557 4627 54106 6632 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060445	congenital stromal corneal dystrophy Aliases: CSCD congenital hereditary stromal dystrophy	DCN	1634	Homo sapiens (human)	Alliance of Genome Resources
DOID:8947	diabetic retinopathy Aliases: Retinal abnormality - diabetes-related	Insr	16337	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11717	neonatal diabetes mellitus Aliases: diabetes mellitus syndrome in newborn infant neonatal diabetes	Ins2	16334	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050524	maturity-onset diabetes of the young Aliases: MODY Mason-type diabetes	Ins2 Pdx1 Tgm2	16334 18609 21817	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060639	permanent neonatal diabetes mellitus Aliases: PDMI PNDM permanent diabetes mellitus of infancy	Ins2 Kcnj11	16334 16514	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080978	arthrogryposis multiplex congenita-1	LGI4	163175	Homo sapiens (human)	Alliance of Genome Resources
DOID:1825	childhood absence epilepsy Aliases: petit mal seizure pyknolepsy	CACNA1H GABRB3 GABRG2 GRIK1 LGI4 SLC2A1	163175 2562 2566 2897 6513 8912	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111153	congenital mirror movement disorder Aliases: familial congenital controlateral synkinesia familial congenital mirror movements hereditary congenital controlateral synkinesia hereditary congenital mirror movements isolated congenital controlateral synkinesia isolated congenital mirror movements	DCC NTN1	1630 9423	Homo sapiens (human)	Alliance of Genome Resources
DOID:9269	maple syrup urine disease Aliases: Ketoacidaemia branched chain ketoaciduria	BCKDHA BCKDHB DBT DLD	1629 1738 593 594	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090145	dopamine beta-hydroxylase deficiency Aliases: congenital dopamine beta-hydroxylase deficiency noradrenaline deficiency norepinephrine deficiency	DBH HSPA5	1621 3309	Homo sapiens (human)	Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	ATP1A2 CACNA1A DBH DRD2	1621 1813 477 773	Homo sapiens (human)	Alliance of Genome Resources
DOID:10534	stomach cancer Aliases: gastric cancer gastric neoplasm	Il6st	16195	Mus musculus (house mouse)	Alliance of Genome Resources

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