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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 **5501 - 5525** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:916	liver benign neoplasm Aliases: epithelial hepatic and intrahepatic bile duct neoplasm	aldo-1	176788	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9869	hereditary fructose intolerance syndrome Aliases: Fructosaemia Fructose-1,6-bisphosphate aldolase B deficiency Fructosemia	aldo-1	176788	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050816	urofacial syndrome Aliases: Ochoa syndrome hydronephrosis with peculiar facial expression	sma-10	176849	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1386	abetalipoproteinemia Aliases: familial hypobetalipoproteinemia microsomal triglyceride transfer protein deficiency disease	dsc-4	176852	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080412	familial adenomatous polyposis 4	Msh3	17686	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080557	congenital disorder of glycosylation Ie Aliases: congenital disorder of glycosylation 1e	dpm-1	176874	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070272	hereditary nonpolyposis colorectal cancer type 5 Aliases: HNPCC5	Msh6	17688	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1934	dysostosis	apx-1 efn-4	176882 178759	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060668	anencephaly	efn-4	176882	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14737	craniofrontonasal syndrome Aliases: CFND CFNS craniofrontonasal dysostosis craniofrontonasal dysplasia	efn-4	176882	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112164	spermatogenic failure 46 Aliases: SPGF46	DNAH8	1769	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111535	progressive osseous heteroplasia Aliases: POH ectopic ossification familial type familial ectopic ossification osteoma cutis	dbl-1 ost-1	176931 179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110338	osteogenesis imperfecta type 17 Aliases: OI17 osteogenesis imperfecta type XVII	ost-1	176931	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2152	ovary epithelial cancer Aliases: Ovarian Surface epithelial-Stromal tumor	ost-1	176931	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112001	immunodeficiency 50 Aliases: CID due to Moesin deficiency IMD50 MSN-related combined immunodeficiency X-linked Moesin-associated immunodeficiency combined immunodeficiency due to Moesin deficiency immunodeficiency 50 X linked recessive	Msn	17698	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9719	neovascular inflammatory vitreoretinopathy Aliases: ADNIV Retinitis proliferans autosomal dominant neovascular inflammatory vitreoretinopathy proliferative vitreoretinopathy	AGER APOA4 BDNF CAT EDN1 HGF ICAM1 IGFBP6 IL6 KNG1 LRP5 LTA SERPINF1	177 1906 3082 337 3383 3489 3569 3827 4041 4049 5176 627 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:1891	optic nerve disease Aliases: disorder of the second nerve optic nerve disorder optic neuropathy	ACO2 AGER EDN1	177 1906 50	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050850	diabetic encephalopathy	AGER APP GSK3B NGFR PPARG	177 2932 351 4804 5468	Homo sapiens (human)	Alliance of Genome Resources
DOID:2508	Takayasu's arteritis Aliases: Aortic arch arteritis Idiopathic aortitis Takayasu arteritis Takayasu's disease aortic arch syndrome	AGER HLA-A HLA-B HLA-DRB1 IL2 MMP3 MMP9	177 3105 3106 3123 3558 4314 4318	Homo sapiens (human)	Alliance of Genome Resources
DOID:77	gastrointestinal system disease Aliases: GIT disease Gastroenteropathy alimentary system disease digestive system disorder gastrointestinal disease gastrointestinal disorder	AGER IGF2 MECP2 TF VCAM1	177 3481 4204 7018 7412	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050697	chorioamnionitis	AGER FAS IL6 LTA MBL2 MMP9 TGFB1 TNF TREM1	177 355 3569 4049 4153 4318 54210 7040 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:520	aortic disease Aliases: aortic disorder disorder of the aorta	AGER SMAD4 VCAM1	177 4089 7412	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080832	mild cognitive impairment	AGER NEFL SLC6A3	177 4747 6531	Homo sapiens (human)	Alliance of Genome Resources
DOID:8515	Cor pulmonale Aliases: cardiopulmonary disease pulmonary heart disease	AGER CX3CL1 TNF	177 6376 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:9540	vascular skin disease	AGER	177	Homo sapiens (human)	Alliance of Genome Resources

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