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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 **9376 - 9400** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:643	progressive multifocal leukoencephalopathy	Nefl	83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110149	Charcot-Marie-Tooth disease type 1F Aliases: CMT1F Charcot-Marie-Tooth neuropathy type 1F	Nefl	83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080294	Charcot-Marie-Tooth disease dominant intermediate G	Nefl	83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110165	Charcot-Marie-Tooth disease type 2E Aliases: CMT2E Charcot-Marie-Tooth neuropathy type 2E autosomal dominant Charcot-Marie-Tooth disease type 2E	Nefl	83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10976	membranous glomerulonephritis Aliases: membranous nephropathy	Nep1 Nep4 Tsf2	31547 39435 42449	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:13250	diarrhea	Nep1 Nep4	31547 42449	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111745	cerebellar ataxia type 43 Aliases: SCA43	Nep1 Nep4	31547 42449	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9246	cerebral amyloid angiopathy Aliases: Cerebral Hemorrhage, Hereditary, with Amyloidosis Hereditary Cerebral Hemorrhage with Amyloidosis	Nep1 Nep4	31547 42449	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T Aliases: AR-CMT2T CMT2T Charcot-Marie-Tooth neuropathy type 2T autosomal recessive axonal Charcot-Marie-Tooth disease type 2T	Nep1 Nep4	31547 42449	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050646	distal arthrogryposis Aliases: Arthrogryposis Multiplex Congenita	Nep2 goe	32660 40588	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111594	distal arthrogryposis type 5D Aliases: DA5D distal arthrogryposis type 5 without ophthalmoparesis distal arthrogryposis type 5 without ophthalmoplegia	Nep2 goe	32660 40588	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:10825	essential hypertension Aliases: idiopathic hypertension primary hypertension	Nep3 btl htl nrv1 nrv2	33005 33952 33953 39564 42160	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:6406	double outlet right ventricle Aliases: Dextrotransposition of aorta Double outlet right ventricle with subpulmonary ventricular septal defect Taussig-Bing syndrome or defect	Nep3	33005	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111153	congenital mirror movement disorder Aliases: familial congenital controlateral synkinesia familial congenital mirror movements hereditary congenital controlateral synkinesia hereditary congenital mirror movements isolated congenital controlateral synkinesia isolated congenital mirror movements	NetA NetB	32398 32400	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111253	neurofibromatosis 1 Aliases: NF1 Peripheral Neurofibromatosis Recklinghausen's neurofibromatosis neurofibromatosis type I von Recklinghausen Disease	Nf1 Vegfa	18015 22339	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4992	optic nerve glioma Aliases: glioma of the optic nerve	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070483	Watson syndrome	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8712	neurofibromatosis	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070482	spinal neurofibromatosis Aliases: FNSF SNF familial spinal neurofibromatosis	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111683	neurofibromatosis-Noonan syndrome Aliases: NFNS Noonan neurofibromatosis syndrome neurofibromatosis type 1-Noonan syndrome neurofibromatosis with Noonan phenotype	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5151	plexiform neurofibroma	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13619	extrahepatic cholestasis Aliases: extrahepatic biliary Stasis extrahepatic obstructive biliary disease	Nfe2l2 Oprm1 Pdgfrb Slc22a1 Slc22a2	24629 24904 25601 29503 83619	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060409	NFIA-related disorder Aliases: 1p31p32 microdeletion syndrome Chromosome 1, Monosomy 1p32 brain malformations with or without urinary tract defects chromosome 1p32-p31 deletion syndrome	Nfia	18027	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13300	Scheuermann's disease Aliases: Juvenile osteochondritis of the spine Juvenile osteochondrosis of Scheurermann Juvenile osteochondrosis of spine Scheuermann's kyphosis Sherman's Disease	Nfix	18032	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050858	Marshall-Smith syndrome	Nfix	18032	Mus musculus (house mouse)	Alliance of Genome Resources

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