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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **401 - 425** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism
DOID:2747	glycogen storage disease Aliases: glycogenosis	gyg1a gyg1b gys2	373082 406831 415152	Danio rerio (zebrafish)
DOID:2747	glycogen storage disease Aliases: glycogenosis	gyg1.L gyg1.S	446485 779133	Xenopus laevis (African clawed frog)
DOID:0050579	glycogen storage disease XV Aliases: Glycogen storage disease 15 Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency glycogen storage disease type XV	gyg1.L gyg1.S	446485 779133	Xenopus laevis (African clawed frog)
DOID:2747	glycogen storage disease Aliases: glycogenosis	gyg1	394883	Xenopus tropicalis (tropical clawed frog)
DOID:0050579	glycogen storage disease XV Aliases: Glycogen storage disease 15 Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency glycogen storage disease type XV	gyg1	394883	Xenopus tropicalis (tropical clawed frog)
DOID:0050579	glycogen storage disease XV Aliases: Glycogen storage disease 15 Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency glycogen storage disease type XV	gyg-1 gyg-2	180119 180644	Caenorhabditis elegans
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	gsy-1	174924	Caenorhabditis elegans
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	gsy-1	174924	Caenorhabditis elegans
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	gspd-1	178046	Caenorhabditis elegans
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	gspd-1	178046	Caenorhabditis elegans
DOID:9279	hyperhomocysteinemia	gspd-1	178046	Caenorhabditis elegans
DOID:12365	malaria Aliases: induced malaria	gspd-1	178046	Caenorhabditis elegans
DOID:0050328	congenital hypothyroidism	gspd-1	178046	Caenorhabditis elegans
DOID:13628	favism	gspd-1	178046	Caenorhabditis elegans
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	gspd-1	178046	Caenorhabditis elegans
DOID:2383	neonatal jaundice Aliases: neonatal hyperbilirubinemia neonatal icterus	gspd-1	178046	Caenorhabditis elegans
DOID:2355	anemia Aliases: anaemia	gspd-1	178046	Caenorhabditis elegans
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	gspd-1	178046	Caenorhabditis elegans
DOID:1591	renovascular hypertension	gspd-1	178046	Caenorhabditis elegans
DOID:14067	Plasmodium falciparum malaria Aliases: Malaria fever, subtertian falciparum malaria malignant tertian fever	gspd-1	178046	Caenorhabditis elegans
DOID:13580	cholestasis Aliases: Obstruction of bile duct bile occlusion	gspd-1	178046	Caenorhabditis elegans
DOID:0080208	metabolic dysfunction-associated steatotic liver disease Aliases: MAFLD MASLD NAFLD metabolic dysfunction-associated fatty liver disease metabolic dysfunction-related steatotic liver disease metabolic-associated fatty liver disease non-alcoholic fatty liver disease nonalcoholic fatty liver disease	gspd-1	178046	Caenorhabditis elegans
DOID:557	kidney disease Aliases: impaired renal function disease nephropathy	gspd-1 sqv-6	178046 190099	Caenorhabditis elegans
DOID:583	hemolytic anemia Aliases: ANEMIA HEMOLYTIC	gspd-1 pgk-1	171965 178046	Caenorhabditis elegans
DOID:224	transient cerebral ischemia Aliases: TIA TIA - Transient ischaemic attack Transient cerebral ischaemia Transient ischemic attacks transient ischemic attack	gspd-1 parp-1	178046 266823	Caenorhabditis elegans

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