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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 **10201 - 10225** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:5394	prolactinoma Aliases: PITUITARY ADENOMA, PROLACTIN-SECRETING Prolactinoma of Pituitary gland familial prolactinoma	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:0080313	cleft palate-lateral synechia syndrome Aliases: CPLS syndrome syngnathia	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:668	myositis ossificans Aliases: Myisitis ossificans Ossification - muscle	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:18	urinary system disease Aliases: Non-neoplastic urinary tract disease urinary tract disease	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:540	strabismus	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12185	otosclerosis	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:12556	acute kidney tubular necrosis Aliases: ATN - acute tubular necrosis acute renal Failure with tubular necrosis acute renal failure with lesion of tubular necrosis acute tubular necrosis acute tubule necrosis	dbl-1 svh-2	179068 180929	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11400	pyelonephritis	acn-1 dbl-1	179068 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13515	tuberous sclerosis Aliases: Bourneville's disease Epiloia Tuberose sclerosis Tuberous sclerosis syndrome cerebral sclerosis	W01F3.2 dbl-1 zmp-4	179068 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060887	ossification of the posterior longitudinal ligament of spine Aliases: OPLL	C27A7.3 dbl-1 enpp-1	179068 179663 179665	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9296	cleft lip Aliases: Labium leporinum cheiloschisis cleft lip, unilateral, complete complete unilateral cleft lip hare lip	dbl-1 folt-1 sdn-1	179068 179544 181259	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080207	CAKUT2 Aliases: Congenital anomalies of the kidney and urinary tract 2	W01F3.2 cri-2 dbl-1 zmp-4	179068 179197 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:885	fascioliasis Aliases: Fasciola hepatica infection Infection by Fasciola Liver flukes Sheep liver fluke infection	cpr-3 cpr-4 cpr-6	179053 180033 180931	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081346	congenital myopathy 14	Myl1	17901	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2748	glycogen storage disease III Aliases: Glycogen storage disease 3 Glycogen storage disease, type III amylo 1,6 glucosidase deficiency deficiency of debranching enzyme deficiency of dextrin	AGL	178	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110314	hypertrophic cardiomyopathy 8 Aliases: cardiomyopathy hypertrophic mid-left ventricular chamber type 1 cardiomyopathy, familial hypertrophic, 8	Myl3	17897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080201	Peters plus syndrome Aliases: Krause-Kivlin syndrome Peters anomaly-short limb dwarfism syndrome Peters-plus syndrome	ZC250.2	178968	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110108	atrial heart septal defect 3 Aliases: ASD3 atrial septal defect 3	Myh6	17888	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110453	dilated cardiomyopathy 1EE Aliases: CMD1EE	Myh6	17888	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110320	hypertrophic cardiomyopathy 14 Aliases: CMH14 cardiomyopathy familial hypertrophic 14	Myh6	17888	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090116	spondylocarpotarsal synostosis syndrome Aliases: SCT congenital scoliosis with unilateral unsegmented bar congenital synspondylism spondylocarpotarsal syndrome spondylocarpotarsal synostosis vertebral fusion with carpal coalition	Flnb Myh6	17888 286940	Mus musculus (house mouse)	Alliance of Genome Resources

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