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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:540	strabismus	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:0080015	physical disorder Aliases: congenital disorder	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080404	orofacial cleft 11 Aliases: nonsyndromic cleft lip with or without cleft palate 11	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:0060306	Meier-Gorlin syndrome Aliases: ear-patella-short stature syndrome	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: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:18	urinary system disease Aliases: Non-neoplastic urinary tract disease urinary tract disease	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: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: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
DOID:0060651	MYH-9 related disease	Myh9	17886	Mus musculus (house mouse)	Alliance of Genome Resources

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