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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 **5751 - 5775** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:18	urinary system disease Aliases: Non-neoplastic urinary tract disease urinary tract disease	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:668	myositis ossificans Aliases: Myisitis ossificans Ossification - muscle	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110122	Axenfeld-Rieger syndrome type 3 Aliases: Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss RIEG3 Rieger syndrome type 3 anterior chamber cleavage syndrome anterior segment mesenchymal dysgenesis	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060306	Meier-Gorlin syndrome Aliases: ear-patella-short stature syndrome	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:540	strabismus	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
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	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080313	cleft palate-lateral synechia syndrome Aliases: CPLS syndrome syngnathia	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11963	esophagitis Aliases: acute esophagitis	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5394	prolactinoma Aliases: PITUITARY ADENOMA, PROLACTIN-SECRETING Prolactinoma of Pituitary gland familial prolactinoma	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080205	CAKUT Aliases: Congenital anomalies of the kidney and urinary tract Renal or urinary tract malformation	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111805	syndromic microphthalmia 6 Aliases: Bakrania-Ragge syndrome MCOPS6 anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia microphthalmia and pituitary anomalies microphthalmia with brain and digit anomalies syndromic microphthalmia type 6	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1882	atrial heart septal defect Aliases: atrial septal defect atrioseptal defect auricular septal defect congenital atrial septal defect interatrial septal defect interauricular septal defect	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080288	spinocerebellar ataxia 46	F09G2.8	179105	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13141	uveitis	acn-1 srp-6 srp-7	179125 179195 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110536	autosomal recessive nonsyndromic deafness 91 Aliases: DFNB91 autosomal recessive deafness 91	srp-6 srp-7	179125 179195	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060832	Griscelli syndrome type 1 Aliases: GS1 Griscelli syndrome with neurological impairment Griscelli syndrome, cutaneous and neurological type Griscelli-Prunieras syndrome type 1 hypopigmentation-neurologic impairment syndrome	Myo5a	17918	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080559	congenital disorder of glycosylation Ig Aliases: ALG12-congenital disorder of glycosylation congenital disorder of glycosylation 1g	algn-12	179185	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	cri-2 timp-1 ver-4	179197 179199 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2006	preretinal fibrosis Aliases: Macular puckering of retina Macular retinal puckering cellophane maculopathy	cri-2 timp-1	179197 179199	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13099	Moyamoya disease Aliases: progressive intracranial arterial occlusion	cri-2 timp-1	179197 179199	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14250	Down syndrome Aliases: Complete trisomy 21 syndrome Down's syndrome Down's syndrome - trisomy 21 Downs syndrome G Trisomy trisomy 21 syndrome	W01F3.2 cri-2 pad-2 zmp-4	179197 179991 180351 259529	Caenorhabditis elegans	Alliance of Genome Resources
DOID:178	vascular disease Aliases: vascular tissue disease	cri-2	179197	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090114	Sorsby's fundus dystrophy Aliases: SFD hemorrhagic macular dystrophy pseudoinflammatory fundus dystrophy of Sorsby	cri-2	179197	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110552	autosomal dominant nonsyndromic deafness 22 Aliases: DFNA22 autosomal dominant deafness 22	Myo6	17920	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110495	autosomal recessive nonsyndromic deafness 37 Aliases: DFNB37 autosomal recessive deafness 37	Myo6	17920	Mus musculus (house mouse)	Alliance of Genome Resources

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