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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

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

Displaying entries **4376 - 4400** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:0050644	arterial calcification of infancy Aliases: generalized arterial calcification of infancy idiopathic infantile arterial calcification infantile arteriosclerosis	Enpp1	18605	Mus musculus (house mouse)
DOID:0060887	ossification of the posterior longitudinal ligament of spine Aliases: OPLL	Enpp1	18605	Mus musculus (house mouse)
DOID:0080333	aortic valve disease 1	Enpp1	18605	Mus musculus (house mouse)
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	Enpp1 Gys1 Ppargc1a	690987 83516 85496	Rattus norvegicus (Norway rat)
DOID:10754	otitis media	Enpp1 Tlr4 Tnf	24835 29260 85496	Rattus norvegicus (Norway rat)
DOID:1214	tympanosclerosis	Enpp1 Tlr4	29260 85496	Rattus norvegicus (Norway rat)
DOID:1123	spondyloarthropathy Aliases: spondarthropathy spondylarthrosis	Enpp1 Tnf	24835 85496	Rattus norvegicus (Norway rat)
DOID:2738	pseudoxanthoma elasticum Aliases: Gronblad-Strandberg syndrome	Enpp1 Xylt1 Xylt2	64133 64134 85496	Rattus norvegicus (Norway rat)
DOID:0050644	arterial calcification of infancy Aliases: generalized arterial calcification of infancy idiopathic infantile arterial calcification infantile arteriosclerosis	Enpp1	85496	Rattus norvegicus (Norway rat)
DOID:0060887	ossification of the posterior longitudinal ligament of spine Aliases: OPLL	Enpp1	85496	Rattus norvegicus (Norway rat)
DOID:0080333	aortic valve disease 1	Enpp1	85496	Rattus norvegicus (Norway rat)
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	Eogt	101351	Mus musculus (house mouse)
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	Eogt N	31293 33424	Drosophila melanogaster (fruit fly)
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	Eogt	494219	Rattus norvegicus (Norway rat)
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	Epm2a Gys1 Gys2 Nhlrc1	114005 25623 364682 690987	Rattus norvegicus (Norway rat)
DOID:891	progressive myoclonus epilepsy Aliases: PME progressive myoclonic epilepsy	Epm2a	114005	Rattus norvegicus (Norway rat)
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	Epm2a Gys1 Gys2 Nhlrc1	105193 13853 14936 232493	Mus musculus (house mouse)
DOID:891	progressive myoclonus epilepsy Aliases: PME progressive myoclonic epilepsy	Epm2a	13853	Mus musculus (house mouse)
DOID:206	hereditary multiple exostoses Aliases: Multiple congenital exostosis Multiple exostosis syndromes Osteochondromatosis syndrome hereditary multiple exostoses 1 hereditary multiple exostoses 2 hereditary multiple exostoses 3 multiple ostechondromas	Ext1 Ext2 Extl1 Extl3	14042 14043 54616 56219	Mus musculus (house mouse)
DOID:206	hereditary multiple exostoses Aliases: Multiple congenital exostosis Multiple exostosis syndromes Osteochondromatosis syndrome hereditary multiple exostoses 1 hereditary multiple exostoses 2 hereditary multiple exostoses 3 multiple ostechondromas	Ext1 Ext2 Extl1 Extl3	299907 311215 313610 56819	Rattus norvegicus (Norway rat)
DOID:0050565	autosomal recessive nonsyndromic deafness	F38B6.6	185454	Caenorhabditis elegans
DOID:0050570	congenital disorder of glycosylation type I	F52B11.2 ZK632.4 algn-12 algn-1 algn-5 algn-6 algn-8 algn-9 dpm-1	174542 174633 175920 176388 176874 178364 178822 179185 182392	Caenorhabditis elegans
DOID:5212	congenital disorder of glycosylation Aliases: carbohydrate-deficient glycoprotein syndrome	F52B11.2 algn-1 algn-3 bre-4	175065 175920 178364 190668	Caenorhabditis elegans
DOID:0080552	congenital disorder of glycosylation Ia Aliases: PMM2-congenital disorder of glycosylation congenital disorder of glycosylation 1a	F52B11.2	178364	Caenorhabditis elegans
DOID:5804	discrete subaortic stenosis	FADS2	9415	Homo sapiens (human)

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