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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 **15726 - 15750** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0070517	retinal macular dystrophy 2 Aliases: MCDR2	PROM1	8842	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050169	cutaneous lupus erythematosus	Cd40lg	84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050120	hemophagocytic lymphohistiocytosis Aliases: haemophagocytic syndrome	Cd163 Elp1	230233 93671	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080219	dystransthyretinemic hyperthyroxinemia	Ttr	24856	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080046	Stickler syndrome	Col11a1 Col11a2 Col2a1	12814 12815 12824	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110939	autosomal recessive osteopetrosis 5 Aliases: OPTB5 infantile malignant osteopetrosis 3	Ostm1	14628	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3153	lipomatosis Aliases: multiple lipomatosis	Cel	12613	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070355	overactive bladder syndrome Aliases: OAB overactive bladder urge syndrome urgency-frequency syndrome	ngfb	58133	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:3755	antithrombin III deficiency Aliases: AT III deficiency hereditary thrombophilia due to congenital antithrombin deficiency	Serpinc1	11905	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U Aliases: LGMD2U MDDGC7 autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency muscular dystrophy limb-girdle type 2U muscular dystrophy-dystroglycanopathy (limb-girdle) type C7	CRPPA	729920	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080301	atypical hemolytic-uremic syndrome	Adamts13 C3 Cd46 Cfb Cfh Cfhr1 Cfhr2 Cfhr4 Cfi Thbd	12266 12628 12630 14962 17221 214403 21824 279028 50702 545366	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11713	diabetic angiopathy Aliases: Diabetic vascular disorder diabetic peripheral angiopathy	pon2	448598	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0080799	sinonasal undifferentiated carcinoma	SNF5	852592	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13884	sick sinus syndrome Aliases: sinus node infection	Agt Hcn1 Hcn4 Scn5a	24179 25665 59266 84390	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9975	cocaine dependence	acr-2 acr-3 dop-2 gbb-1 glr-1 glr-2 lev-1 ten-1 unc-38 unc-63	172105 172150 175953 175999 176204 178269 179347 180936 180937 189837	Caenorhabditis elegans	Alliance of Genome Resources
DOID:801	hemarthrosis Aliases: Haemarthrosis of shoulder joint Haemarthrosis of the ankle and foot Haemarthrosis of the pelvic region and thigh Hemarthrosis involving ankle and foot Hemarthrosis involving forearm Hemarthrosis involving hand Hemarthrosis involving lower leg Hemarthrosis involving pelvic region and thigh Hemarthrosis involving shoulder region Hemarthrosis involving upper arm Hemarthrosis of ankle and/or foot Hemarthrosis of forearm Hemarthrosis of hand Hemarthrosis of lower leg Hemarthrosis of shoulder Hemarthrosis of shoulder region Hemarthrosis of the ankle and foot Hemarthrosis of the ankle and/or foot Hemarthrosis of the forearm Hemarthrosis of the hand Hemarthrosis of the lower leg Hemarthrosis of the pelvic region and thigh Hemarthrosis of the shoulder region Hemarthrosis of the upper arm Hemarthrosis of upper arm	F8	2157	Homo sapiens (human)	Alliance of Genome Resources
DOID:8692	myeloid leukemia Aliases: Non-Lymphocytic Leukemia leukaemia myelogenous leukemia myelogenous myeloid granulocytic leukaemia myeloid granulocytic leukemia myeloid leukaemia	Ugt301D1 Ugt302K1 Ugt303A1 Ugt304A1 Ugt316A1 Ugt35A1 Ugt35C1 Ugt35E2 Ugt36D1 Ugt36E1 Ugt36F1 Ugt37A3 Ugt37C1 Ugt37D1 Ugt37E1 Ugt49B2 htl tor	35105 35137 35138 35139 35717 40079 41334 41574 42160 42538 53501 53502 53503 53506 53507 53511 53512 53583	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:437	myasthenia gravis	Ache Chrm1 Cxcr3 Esr2 Fas Il2rb Musk	246097 25149 25229 25746 81725 83817 84475	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050462	Antley-Bixler syndrome with disordered steroidogenesis Aliases: trapezoidocephaly-synostosis syndrome	Por	18984	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:118	pericardial effusion	IL10	3586	Homo sapiens (human)	Alliance of Genome Resources
DOID:4989	pancreatitis	ECM14	856533	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2436	glomangioma Aliases: Glomuvenous Malformation	GLMN	11146	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112348	hereditary spastic paraplegia 78 Aliases: SPG78 spastic paraplegia 78 autosomal recessive	Atp13a2	74772	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:0060244	specific language impairment	Cntnap2	66797	Mus musculus (house mouse)	Alliance of Genome Resources

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