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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	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4876 - 4900** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:8725	vascular dementia Aliases: Multi Infarct Dementia multifocal dementia	Gsk3b Tnf Tp53	24835 24842 84027	Rattus norvegicus (Norway rat)
DOID:0050861	colorectal adenocarcinoma	Gsk3b Tp53	24842 84027	Rattus norvegicus (Norway rat)
DOID:90	degenerative disc disease Aliases: cervical disc degenerative disease intervertebral disc degeneration lumbar disc degeneration vertebral disc disease	Gsk3b	84027	Rattus norvegicus (Norway rat)
DOID:303	substance-related disorder	Gsk3b	84027	Rattus norvegicus (Norway rat)
DOID:0050850	diabetic encephalopathy	Gsk3b	84027	Rattus norvegicus (Norway rat)
DOID:12798	mucopolysaccharidosis	Gusb Hyal1	110006 15586	Mus musculus (house mouse)
DOID:12803	Sly syndrome Aliases: MPS VII - Sly syndrome beta-glucuronidase deficiency deficiency of beta-glucuronidase mucopolysaccharidosis VII	Gusb	110006	Mus musculus (house mouse)
DOID:12798	mucopolysaccharidosis	Gusb Hyal1	24434 367166	Rattus norvegicus (Norway rat)
DOID:8283	peritonitis Aliases: Retractile mesenteritis acute generalized peritonitis primary bacterial peritonitis sclerosing mesenteritis	Gusb Tnf	24434 24835	Rattus norvegicus (Norway rat)
DOID:12803	Sly syndrome Aliases: MPS VII - Sly syndrome beta-glucuronidase deficiency deficiency of beta-glucuronidase mucopolysaccharidosis VII	Gusb	24434	Rattus norvegicus (Norway rat)
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	37419	Drosophila melanogaster (fruit fly)
DOID:2747	glycogen storage disease Aliases: glycogenosis	Gyg1 Gys2 Pfkl Pfkm Pfkp Phka1 Phka2 Phkg2 Prkag2 Pygl	108099 110094 110095 18641 18642 18679 232493 27357 56421 68961	Mus musculus (house mouse)
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	27357	Mus musculus (house mouse)
DOID:2747	glycogen storage disease Aliases: glycogenosis	Gyg1 Gys2 Pfkl Pfkm Pfkp Phkg2 Pygl	140671 25623 25741 60416 64035 65152 81675	Rattus norvegicus (Norway rat)
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	81675	Rattus norvegicus (Norway rat)
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	H12D21.10	179990	Caenorhabditis elegans
DOID:0090141	cortisone reductase deficiency 1 Aliases: CORTRD1	H6PD	9563	Homo sapiens (human)
DOID:0090139	cortisone reductase deficiency Aliases: CORTRD	H6pd	100198	Mus musculus (house mouse)
DOID:0090141	cortisone reductase deficiency 1 Aliases: CORTRD1	H6pd	100198	Mus musculus (house mouse)
DOID:0040084	Streptococcus pneumonia	HACD1 MASP2 MBL2 PKD1 PTGS1 PTGS2 STS	10747 412 4153 5310 5742 5743 9200	Homo sapiens (human)
DOID:401	multidrug-resistant tuberculosis	HACD1 NCAM1 PTGS2 RENBP SMUG1	23583 4684 5743 5973 9200	Homo sapiens (human)
DOID:0081337	congenital myopathy	HACD1	9200	Homo sapiens (human)
DOID:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	HACD1	9200	Homo sapiens (human)
DOID:0070215	familial hyperinsulinemic hypoglycemia 4 Aliases: HHF4 hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency hyperinsulinism due to SCHAD deficiency hyperinsulinism due to glutamodehydrogenase deficiency hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency	HADH	3033	Homo sapiens (human)
DOID:13789	staphyloma posticum	HADHA	3030	Homo sapiens (human)

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