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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 **9826 - 9850** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:10587	Krabbe disease Aliases: Diffuse globoid body sclerosis GLOBOID CELL LEUKOENCEPHALOPATHY Galactosylceramide beta-galactosidase deficiency Krabbe's disease Krabbe's leukodystrophy beta galactocerebrosidase deficiency globoid cell leukodystrophy	C29E4.10	183002	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13276	Mycoplasma pneumoniae pneumonia Aliases: Mycoplasma pneumonia Mycoplasmal pneumonia Pneumonia due to Eaton's agent Pneumonia due to Mycoplasma pneumoniae Pneumonia due to Mycoplasma pneumoniae (disorder) cold agglutinin positive pneumonia	C29E4.10	183002	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11949	Creutzfeldt-Jakob disease Aliases: CJD Creutzfeldt Jacob syndrome Creutzfeldt Jakob disease Creutzfeldt-Jacob disease Jakob-Creutzfeldt disease Subacute spongiform encephalopathy Transmissible virus dementia	C29E4.10	183002	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060851	pemphigus vulgaris Aliases: familial pemphigus vulgaris	DSG3 HLA-DQB1	1830 3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:11111	hydronephrosis	AGT HAVCR1 LCN2 TBXAS1	183 26762 3934 6916	Homo sapiens (human)	Alliance of Genome Resources
DOID:1580	diffuse scleroderma Aliases: diffuse systemic sclerosis systemic sclerosis, diffuse	ADIPOQ AGT FCGR2A HLA-DQA1 IL10 IL13 IL6 IRAK1 KDR STAT4 TAP1 TLR2	183 2212 3117 3569 3586 3596 3654 3791 6775 6890 7097 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:1312	focal segmental glomerulosclerosis Aliases: FGS FSGS focal glomerular sclerosis focal glomerulosclerosis	ACTN4 AGT AGTR1 AGTR2 ANGPT2 CASP9 CD2AP CMAS HSPB1 LIPC LPL MMP2 MMP9 MYO9A PIAS1 PPP3CA SERPINE1 SHH SRGAP1 TMEM63C TRPC6 VLDLR VWF	183 185 186 23607 285 3315 3990 4023 4313 4318 4649 5054 5530 55907 57156 57522 6469 7225 7436 7450 81 842 8554	Homo sapiens (human)	Alliance of Genome Resources
DOID:3314	angiomyolipoma	Ogg1 Stat3	18294 20848	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070468	Yoon-Bellen neurodevelopmental syndrome Aliases: YOBELN	Ogdh	18293	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081326	oxoglutarate dehydrogenase deficiency Aliases: Oxoglutaric aciduria alpha-ketoglutarate dehydrogenase deficiency	Ogdh	18293	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110458	dilated cardiomyopathy 1BB Aliases: CMD1BB	DSG2	1829	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110081	arrhythmogenic right ventricular dysplasia 10 Aliases: ARVC10 ARVD10 arrhythmogenic right ventricular cardiomyopathy 10 familial arrhythmogenic right ventricular dysplasia 10	DSG2	1829	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081108	keratosis palmoplantaris striata 1	DSG1	1828	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13 Aliases: MDDGA13 Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13	bgnt-1.4 bgnt-1.5	182795 3565692	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8929	atrophic gastritis Aliases: gastric atrophy	nkb-1	182726	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0040090	autoimmune gastritis	nkb-1	182726	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110593	autosomal dominant nonsyndromic deafness 9 Aliases: DFNA9 autosomal dominant deafness 9	C16E9.1	182693	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C16D9.6	182687	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050667	alcohol-related neurodevelopmental disorder Aliases: ARND static encephalopathy	C15H9.4	182643	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111607	distal arthrogryposis type 3 Aliases: DA3 Gordon syndrome camptodactyly-cleft palate-clubfoot syndrome distal arthrogryposis multiplex congenita type IIA	pezo-1	182492	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111576	dehydrated hereditary stomatocytosis 1 Aliases: PSHK1 dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema pseudohyperkalemia edinburgh pseudohyperkalemia familial 1, due to red cell leak	pezo-1	182492	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111608	distal arthrogryposis type 5 Aliases: DA5 DAIIB arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome distal arthrogryposis type IIB distal arthrogryposis with ophthalmoplegia oculomelic amyoplasia	pezo-1	182492	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111795	congenital nystagmus 6 Aliases: NYS6 X-linked congenital nystagmus 6	Gpr143	18241	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050633	ocular albinism 1 Aliases: Albinism ocular 1 ocular albinism	Gpr143 Tyr	18241 22173	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110082	arrhythmogenic right ventricular dysplasia 11 Aliases: ARVC11 ARVD11 arrhythmogenic right ventricular cardiomyopathy 11 familial arrhythmogenic right ventricular dysplasia 11	DSC2	1824	Homo sapiens (human)	Alliance of Genome Resources

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