GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4326 - 4350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:9790	toxocariasis Aliases: Infection by Toxascaris Toxocara infection visceral larva migrans	Il4	16189	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9733	renal tuberculosis Aliases: Tuberculosis of kidney	Il4ra	16190	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9362	status asthmaticus Aliases: Asthma with status asthmaticus Severe asthma attack	Il5 Mpo	16191 17523	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4031	eosinophilic gastroenteritis	Il5	16191	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3044	food allergy Aliases: food hypersensitivity	Il5	16191	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080545	hyper IgE syndrome Aliases: hyper immunoglobulin E syndrome	Il6ra	16194	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11613	hyperandrogenism Aliases: hyperandrogenization syndrome	Il6st Pomc Pparg Prl3c1	16195 18976 19016 27372	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080596	hyper IgE recurrent infection syndrome 4	Il6st	16195	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13777	epidermodysplasia verruciformis	Il7 Tmc6 Tmc8	16196 217353 217356	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	ATP1A2 CACNA1A DBH DRD2	1621 1813 477 773	Homo sapiens (human)	Alliance of Genome Resources
DOID:10762	portal hypertension	ALOX5 ANGPT2 AVP AVPR1A BDKRB2 CCL2 CPEB1 CPEB4 CX3CL1 DBH EDN1 EDNRA EDNRB F5 FGFR2 HSP90AA1 MTOR NGFR NOS1 NOS3 NR1D1 PRL PTEN PTGS2 REN SERPINF1 TMEM67 TNF VASH1 VEGFA	1621 1906 1909 1910 2153 2263 22846 240 2475 285 3320 4804 4842 4846 5176 551 552 5617 5728 5743 5972 624 6347 6376 64506 7124 7422 80315 91147 9572	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090145	dopamine beta-hydroxylase deficiency Aliases: congenital dopamine beta-hydroxylase deficiency noradrenaline deficiency norepinephrine deficiency	DBH HSPA5 SLC6A2 SLC6A3	1621 3309 6530 6531	Homo sapiens (human)	Alliance of Genome Resources
DOID:9269	maple syrup urine disease Aliases: Ketoacidaemia branched chain ketoaciduria	BCKDHA BCKDHB DBT DLD	1629 1738 593 594	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111153	congenital mirror movement disorder Aliases: familial congenital controlateral synkinesia familial congenital mirror movements hereditary congenital controlateral synkinesia hereditary congenital mirror movements isolated congenital controlateral synkinesia isolated congenital mirror movements	DCC NTN1	1630 9423	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080978	arthrogryposis multiplex congenita-1	LGI4	163175	Homo sapiens (human)	Alliance of Genome Resources
DOID:2997	Sertoli-Leydig cell tumor	Inha	16322	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111108	maturity-onset diabetes of the young type 10 Aliases: MODY10	Ins1 Ins2	16333 16334	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10605	short bowel syndrome Aliases: acquired short bowel syndrome short gut syndrome	Clmp Insr Lep Lepr	16337 16846 16847 71566	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050470	Donohue syndrome Aliases: Leprechaunism	Insr	16337	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070220	familial hyperinsulinemic hypoglycemia 5 Aliases: HHF5 hyperinsulinemic hypoglycemia due to INSR deficiency hyperinsulinemic hypoglycemia due to insulin receptor deficiency hyperinsulinism due to INSR deficiency	Insr	16337	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060445	congenital stromal corneal dystrophy Aliases: CSCD congenital hereditary stromal dystrophy	DCN	1634	Homo sapiens (human)	Alliance of Genome Resources
DOID:988	mitral valve prolapse Aliases: Barlow's syndrome floppy mitral valve	ACE AGT DCHS1 DES DZIP1 FBN1 FLNA HLA-B PLAU TSHR	1636 1674 183 2200 22873 2316 3106 5328 7253 8642	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060224	atrial fibrillation Aliases: A-fib AFib	ACE AGER AGT AGTR1 ANK2 CAND2 CD36 CD40 EDN1 FLT1 GP6 HGF HIF1A IL2 ITGAM KCNE1 KCNE2 KCNJ5 KCNQ1 MMP1 MMP2 MMP3 MMP9 RBM20 REN ROBO1 SLC8A1 SLIT2 SOD1 TFPI TGFB1 TLR2 TNF TTN VEGFA VWF	1636 177 183 185 1906 23066 2321 282996 287 3082 3091 3558 3684 3753 3762 3784 4312 4313 4314 4318 51206 5972 6091 6546 6647 7035 7040 7097 7124 7273 7422 7450 9353 948 958 9992	Homo sapiens (human)	Alliance of Genome Resources
DOID:8805	intermediate coronary syndrome Aliases: Angina at rest Anginal chest pain at rest Impending infarction Preinfarction angina Unstable angina Worsening angina	ACE AGT AGTR1 AKT1 APOA4 BDNF EDN1 F7 HMGCR ITGA2 ITGAM ITIH4 MMP1 PTEN SELP SERPINC1 SOD3	1636 183 185 1906 207 2155 3156 337 3673 3684 3700 4312 462 5728 627 6403 6649	Homo sapiens (human)	Alliance of Genome Resources
DOID:14499	Fabry disease Aliases: Alpha-galactosidase A deficiency Angiokeratoma Corporis Diffusum Fabry Disease, Cardiac Variant Fabry's disease alpha galactosidase deficiency deficiency of melibiase	ACE AGT GLA IL1A NAGA	1636 183 2717 3552 4668	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources

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