GlyCosmos Portal

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

Displaying entries **4526 - 4550** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:557	kidney disease Aliases: impaired renal function disease nephropathy	G6pd Kl Tnf Xylt1	24377 24835 64133 83504	Rattus norvegicus (Norway rat)
DOID:12365	malaria Aliases: induced malaria	G6pd Pklr Tnf	24377 24651 24835	Rattus norvegicus (Norway rat)
DOID:0050328	congenital hypothyroidism	G6pd Ppargc1a	24377 83516	Rattus norvegicus (Norway rat)
DOID:13580	cholestasis Aliases: Obstruction of bile duct bile occlusion	G6pd Prkaa1	24377 65248	Rattus norvegicus (Norway rat)
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:2383	neonatal jaundice Aliases: neonatal hyperbilirubinemia neonatal icterus	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:13628	favism	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:224	transient cerebral ischemia Aliases: TIA TIA - Transient ischaemic attack Transient cerebral ischaemia Transient ischemic attacks transient ischemic attack	G6pd2 G6pdx Got1 Nampt Ogg1 Pcna Sirt6 Tnf Ucp2	14380 14381 14718 18294 18538 21926 22228 50721 59027	Mus musculus (house mouse)
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	G6pd2 G6pdx Gpi1 Hk1	14380 14381 14751 15275	Mus musculus (house mouse)
DOID:2355	anemia Aliases: anaemia	G6pd2 G6pdx Hk1 Tnf	14380 14381 15275 21926	Mus musculus (house mouse)
DOID:557	kidney disease Aliases: impaired renal function disease nephropathy	G6pd2 G6pdx Kat2a Kat2b Kl Klb Lctl Tnf Xylt1	14380 14381 14534 16591 18519 21926 233781 235435 83379	Mus musculus (house mouse)
DOID:0050328	congenital hypothyroidism	G6pd2 G6pdx Ppargc1a	14380 14381 19017	Mus musculus (house mouse)
DOID:13580	cholestasis Aliases: Obstruction of bile duct bile occlusion	G6pd2 G6pdx Prkaa1 Pygm	105787 14380 14381 19309	Mus musculus (house mouse)
DOID:12365	malaria Aliases: induced malaria	G6pd2 G6pdx Tnf	14380 14381 21926	Mus musculus (house mouse)
DOID:2383	neonatal jaundice Aliases: neonatal hyperbilirubinemia neonatal icterus	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)
DOID:13628	favism	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)
DOID:1574	alcohol use disorder Aliases: Ethanol abuse alcohol abuse	GAC1 GIP2 PIG1	850979 854350 856781	Saccharomyces cerevisiae S288C
DOID:13366	Stiff-Person syndrome Aliases: Stiff-man syndrome stiff man syndrome	GAD1 GAD2 GLUL HSD17B4 ISYNA1 PLA2G1B PLA2G2A PLA2G6	2571 2572 2752 3295 51477 5319 5320 8398	Homo sapiens (human)
DOID:0050669	spastic cerebral palsy	GAD1 GAD2	2571 2572	Homo sapiens (human)
DOID:9274	hyperlysinemia	GAD1 GCDH HMGCL PC	2571 2639 3155 5091	Homo sapiens (human)

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