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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 **8351 - 8375** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0081361	spastic quadriplegic cerebral palsy 3 Aliases: CPSQ3	Add1	24170	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11044	gastroschisis	Add1 Igf1r Lrp1	24170 25718 299858	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13809	familial combined hyperlipidemia Aliases: familial multiple lipoprotein-type hyperlipidemia hyperbetalipoproteinemia with prebetalipoproteinemia mixed hyperlipidaemia type IIb hyperlipoproteinemia	Add1 Alpl Apob Lpl Serpine1	24170 24539 24617 25586 54225	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10908	hydrocephalus Aliases: hydrocephalus, X-linked hydrocephalus, nonsyndromic, autosomal recessive	Add1 Aqp1 Aqp4 Hmgb1 Hspd1 Itgb1 L1cam Ntf3 Pomk Ppara	24170 24511 25240 25293 25459 25747 306549 50687 63868 81737	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3328	temporal lobe epilepsy Aliases: epilepsy, temporal lobe	Actb Add1 Agt Aqp4 Avp Cacna1a Cxcr4 Cyfip1 Gdnf Glud1 Grik5 Grin2b Grm1 Hcn1 Kcna1 Map2 Mmp9 Nos1 Ntrk2 Pgf Ptprz1 Reln Shh Slc6a1 Vdac2	24170 24179 24221 24399 24407 24410 24414 24520 24598 24718 25054 25293 25398 25453 25595 25613 29499 308666 60628 79212 81687 81822 83531 84390 94203	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency	Acadm	24158	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2320	obstructive lung disease Aliases: respiratory airway obstruction	A2m	24153	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10113	trypanosomiasis	A2m Il4	24153 287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13208	background diabetic retinopathy Aliases: Non proliferative diabetic retinopathy Non-Proliferative Diabetic Retinopathy	A2m Pdgfb	24153 24628	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10159	osteonecrosis Aliases: Avascular necrosis of bone aseptic necrosis bone necrosis	A2m Col2a1 Nos3 Plat Proc Tfpi	24153 24600 25268 25412 25692 29436	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050868	hepatocellular adenoma	A2m Hp	24153 24464	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8283	peritonitis Aliases: Retractile mesenteritis acute generalized peritonitis primary bacterial peritonitis sclerosing mesenteritis	A2m Esr1 Esr2 Gusb Plat Tnf	24153 24434 24835 24890 25149 25692	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3526	cerebral infarction Aliases: CVA - Cerebral infarction Cerebral infarct	A2m Ace Adora1 Apob Brinp3 F7 Folh1 Grin1 Hmgb1 Icam1 Ifnb1 Lipg Lta Map2 Pdx1 Pon1 Pon2 Rbp4 Serpine1 Serping1 Slc6a1 Tnf Tnfrsf11b Vim	24153 24310 24408 24481 24617 24835 25008 25341 25459 25464 25595 25703 260320 286901 291437 29290 29535 295703 296851 54225 79212 81818 84024 85309	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10123	pigmentation disease	Asip Kitlg Mmp9	24152 60427 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110411	retinitis pigmentosa 60 Aliases: RP60	PRPF6	24148	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112034	non-syndromic X-linked intellectual disability 9 Aliases: MRX44 MRX9 X-linked mental retardation 44 X-linked mental retardation 9	FTSJ1	24140	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112040	non-syndromic X-linked intellectual disability 100 Aliases: MRX100 X-linked mental retardation 100	KIF4A	24137	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060485	Mowat-Wilson syndrome Aliases: Hirschsprung disease mental retardation syndrome microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease	Zeb2	24136	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111625	ventriculomegaly - cystic kidney disease Aliases: VMCKD congenital nephrosis-cerebral ventriculomegaly syndrome cystic kidney disease with ventriculomegaly ventriculomegaly with cystic kidney disease	Crb2	241324	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111134	focal segmental glomerulosclerosis 9 Aliases: FSGS9	Crb2	241324	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110423	dilated cardiomyopathy 1C Aliases: CMDC1 dilated cardiomyopathy 1C with or without left ventricular noncompaction	Ldb3	24131	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080095	myofibrillar myopathy 4 Aliases: zaspopathy	Ldb3 Pdlim5 Pdlim7	24131 56376 67399	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081337	congenital myopathy	Hacd1 Ldb3	24131 30963	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080588	agammaglobulinemia 5	Lrrc8a	241296	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080212	polycystic kidney disease 4	Pkhd1	241035	Mus musculus (house mouse)	Alliance of Genome Resources

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