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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 **12476 - 12500** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0111611	autosomal recessive spinocerebellar ataxia 4 Aliases: SCA24 SCAR4 SCASI autosomal recessive cerebellar ataxia-saccadic intrusion syndrome spinocerebellar ataxia 24 spinocerebellar ataxia with saccadic intrusions	Vps13a Vps13c	271564 320528	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111590	Cohen syndrome Aliases: COH1 Hypotonia, obesity, and prominent incisors Pepper syndrome	Vps13a Vps13c	271564 320528	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050766	choreaacanthocytosis Aliases: Levine-Critchley syndrome choreo-acanthocytosis	Vps13a Vps13c	271564 320528	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110805	hereditary spastic paraplegia 53 Aliases: SPG53 autosomal recessive spastic paraplegia 53 autosomal recessive spastic paraplegia type 53	Vps37a	52348	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112332	pontocerebellar hypoplasia type 13 Aliases: PCH13	Vps51	68505	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081426	autosomal recessive distal hereditary motor neuronopathy 7	Vwa1	246228	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081426	autosomal recessive distal hereditary motor neuronopathy 7	Vwa1	298683	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111054	von Willebrand's disease 3 Aliases: VWD type 3 VWD3 von Willebrand disease type 3 von Willebrand disease type III	Vwf	22371	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	W01C8.5 W01F3.2 Y43C5A.2 abt-2 ace-1 ace-2 ace-3 acn-1 cht-1 cpd-2 cpi-1 cubn-1 egl-21 gldi-2 gpx-3 gpx-5 klo-1 lev-9 lron-5 nep-11 nep-1 poml-1 poml-2 ptp-3 srp-3 zmp-2 zmp-3 zmp-4	171782 171905 171999 173685 174116 174685 174787 175076 175383 177372 177557 177911 177940 178672 178748 179729 179991 180351 180628 180780 180836 181178 181684 181706 182513 184307 187297 188252	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10223	dermatomyositis Aliases: Polymyositis with skin involvement dermatopolymyositis	W01C8.5 W01F3.2 scav-2 scav-3 zmp-4	176673 176787 179991 180351 180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11394	adult respiratory distress syndrome Aliases: ARDS Non-cardiogenic pulmonary edema Shock lung acute respiratory distress syndrome adult RDS	W01C8.5 W01F3.2 srp-3 srp-6 srp-7 zmp-4	178672 179125 179195 179991 180351 180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9744	type 1 diabetes mellitus Aliases: IDDM insulin-dependent diabetes mellitus type I diabetes mellitus	W01C8.5 W03G11.3 ace-1 ace-2 ace-3 acn-1 cat-1 cht-1 cri-2 glp-1 gpx-3 gpx-5 gspd-1 ida-1 let-23 lev-9 lin-12 ncam-1 pek-1 poml-1 poml-2 smf-1 smf-2 smf-3 sqv-6 timp-1 ugt-22 ugt-26 ugt-62	171905 171999 172085 174462 175076 175591 175807 176282 176286 177044 178046 178330 179197 179199 180418 180628 180780 180836 180837 180939 181178 181334 181706 182513 187297 188252 189173 190099 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3526	cerebral infarction Aliases: CVA - Cerebral infarction Cerebral infarct	W01C8.5 acn-1 gcp-2.1 gpx-3 gpx-5 myrf-1 myrf-2 poml-1 poml-2 snf-11	171999 174614 180386 180780 180836 181178 181229 182513 187297 191770	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2987	familial mediterranean fever Aliases: FMF benign paroxysmal peritonitis	W01C8.5 acn-1 pgp-1 pgp-3 srp-3	178215 178672 180780 180836 181326	Caenorhabditis elegans	Alliance of Genome Resources
DOID:7147	ankylosing spondylitis Aliases: Bekhterev syndrome Bekhterev's disease Marie-Strumpell disease	W01C8.5 acn-1	180780 180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080301	atypical hemolytic-uremic syndrome	W01C8.5 cfh-1	180836 185381	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050156	idiopathic pulmonary fibrosis Aliases: FIBROCYSTIC PULMONARY DYSPLASIA IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL cryptogenic fibrosing alveolitis	W01C8.5 ddr-2 parp-1 zmp-3	178748 180622 180836 266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1875	impotence Aliases: Sexual impotence erectile dysfunction	W01C8.5 hda-4 ver-1 ver-4	175182 180836 181723 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:676	juvenile rheumatoid arthritis Aliases: Pauciarticular onset juvenile chronic arthritis Still's disease acute juvenile rheumatoid arthritis juvenile chronic polyarthritis juvenile idiopathic arthritis monarticular juvenile rheumatoid arthritis pauciarticular juvenile arthritis systemic juvenile rheumatoid arthritis	W01C8.5 lev-9 smf-1 smf-2 smf-3	177044 180836 180939 188252 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112313	brain small vessel disease	W01C8.5 lev-9	180836 188252	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12132	granulomatosis with polyangiitis Aliases: Necrotizing respiratory granulomatosis Wegener granulomatosis, formerly	W01C8.5 scav-2 scav-3	176673 176787 180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11247	disseminated intravascular coagulation Aliases: DIC Defibrination syndrome Diffuse or disseminated intravascular coagulation	W01C8.5 srp-1 srp-3 srp-6 srp-7	178585 178672 179125 179195 180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13809	familial combined hyperlipidemia Aliases: familial multiple lipoprotein-type hyperlipidemia hyperbetalipoproteinemia with prebetalipoproteinemia mixed hyperlipidaemia type IIb hyperlipoproteinemia	W01C8.5 srp-3	178672 180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	W01C8.5	180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111908	thrombophilia due to thrombomodulin defect Aliases: THBD-related bleeding disorder THBD-related coagulopathy THPH12 thrombomodulin-related bleeding disorder thrombomodulin-related coagulopathy	W01C8.5	180836	Caenorhabditis elegans	Alliance of Genome Resources

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