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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	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **2626 - 2650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:3179	inverted papilloma Aliases: Inverted papilloma, squamous cell	HGF KDR VEGFA	3082 3791 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111169	subcortical band heterotopia Aliases: HeCo band heterotopia double cortex syndrome heterotopic cortex subcortical laminar heterotopia	Eml1	68519	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4480	achondroplasia Aliases: Achondroplastic physique Chondrodystrophia osteosclerosis congenita	Acan Npr2	116564 58968	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13252	mesenteric vascular occlusion	ICAM1 TREM1	3383 54210	Homo sapiens (human)	Alliance of Genome Resources
DOID:9206	Barrett's esophagus Aliases: Barrett esophagus Barrett's esophagus with esophagitis Barrett's oesophagus Barrett's ulcer of esophagus Barretts syndrome ulcerative esophagitis	B3gat2 Cthrc1 Fas Igfbp3 Mmp12 Ptgs2 Smo	117033 24484 246097 25273 282836 29527 64544	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9146	visceral leishmaniasis Aliases: Infection by visceral leishmaniasis Kala-Azar	skn-1 smf-1 smf-2 smf-3	177044 177343 180939 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1884	viral hepatitis Aliases: Viral hepatitis with hepatic coma animal viral hepatitis human viral hepatitis	Ifng Il2	116562 25712	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060903	thrombosis	W01F3.2 Y43C5A.2 acn-1 srp-1 srp-3 srp-7 zmp-3 zmp-4	177911 178585 178672 178748 179195 179991 180351 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070367	leukoencephalopathy with vanishing white matter 5 Aliases: Cree leukoencephalopathy	Eif2b5	224045	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080631	Elsahy-Waters syndrome Aliases: branchioskeletogenital syndrome	Cdh11	84407	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3907	lung squamous cell carcinoma Aliases: Epidermoid cell carcinoma of the lung	fgf9.S	378562	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:1003	pelvic inflammatory disease Aliases: PID	Il4 Ptx3	16189 19288	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:898	autosomal dominant polycystic kidney disease Aliases: ADPKD Congenital biliary ectasias POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1	ANGPT2 BICC1 C9 CD14 CFB EDN1 FLNC FOS GFER GPBAR1 IL1RN ITGA8 LATS1 LCN2 LRP2 LRP5 MMP1 MMP9 MTOR MYC NPHP3 PITX2 PKD1 PKD2 PKD2L1 PKD2L2 RPS6KB1 SERPING1 SLC34A1 SPP1 STAT6	151306 1906 2318 2353 2475 2671 27031 27039 285 3557 3934 4036 4041 4312 4318 4609 5308 5310 5311 6198 629 6569 6696 6778 710 735 80114 8516 9033 9113 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110339	osteogenesis imperfecta type 3 Aliases: OI3 osteogenesis imperfecta type III progressively deforming osteogenesis imperfecta with normal sclera	Col1a1 Col1a2	12842 12843	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9784	trichinosis Aliases: Trichinella spiralis infection	YCT1	850671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060419	chromosome 3q29 microdeletion syndrome Aliases: 3q subtelomere deletion syndrome 3q29 microdeletion syndrome 3q29 recurrent deletion 3qter deletion	Bdh1 Dlg1 Dlg2 Dlg4 Hsd17b2 Hsd17b6 Inhca Ltf Meltf Slc51a Trf	106407 13383 13385 15486 17002 22041 23859 27400 30060 71775 71911	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2859	hemoglobin C disease Aliases: Hb-C disease	HBB	3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:1184	nephrotic syndrome	acn-1 asic-1 cdh-4 cpl-1 deg-1 gldi-2 gpx-3 gpx-5 mec-10 mec-4 nep-11 nep-1 srp-1 srp-7 syg-1 syg-2 unc-105 unc-8	173685 174116 174306 174787 175590 177494 178585 179195 180111 180555 180780 181035 181101 181178 181561 181728 182513 191422	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3744	cervical squamous cell carcinoma Aliases: squamous cell carcinoma of cervix squamous cell carcinoma of the Cervix Uteri	ADAR BAX BIRC2 CCR4 CD82 CSF1R FGF7 FGFR3 FOS PDPN TMBIM6 TNFRSF4 TNFSF4 TP53 TYMP	103 10630 1233 1436 1890 2252 2261 2353 329 3732 581 7009 7157 7292 7293	Homo sapiens (human)	Alliance of Genome Resources
DOID:13812	adhesions of uterus Aliases: Band of uterus Intrauterine adhesions Intrauterine synechiae	Kdr Vegfa	25589 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080289	orofaciodigital syndrome XVII	INTU	27152	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080429	developmental and epileptic encephalopathy 24 Aliases: DEE24 early infantile epileptic encephalopathy 24	Hcn1	15165	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090031	D-bifunctional protein deficiency	HSD17B4	3295	Homo sapiens (human)	Alliance of Genome Resources
DOID:4676	uremia Aliases: UREMIA OF renal ORIGIN	C49C8.5 Y43C5A.2 daf-7	175237 177668 177911	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4372	intracranial embolism Aliases: Cerebral embolism with cerebral infarction cerebral embolism	Kl	83504	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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