GlyCosmos Portal

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

Displaying entries **3351 - 3375** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:13812	adhesions of uterus Aliases: Band of uterus Intrauterine adhesions Intrauterine synechiae	KDR VEGFA	3791 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:13832	patent ductus arteriosus Aliases: Patent ductus Botalli	ACTA1 ACTA2 ACTB ACTBL2 ACTC1 ACTG1 MYH11 PTGIS TFAP2B	345651 4629 5740 58 59 60 70 7021 71	Homo sapiens (human)	Alliance of Genome Resources
DOID:1387	hypolipoproteinemia Aliases: Hypolipoproteinaemia	ABCA1 APOA1	19 335	Homo sapiens (human)	Alliance of Genome Resources
DOID:1388	Tangier disease Aliases: familial alpha-lipoprotein deficiency familial high density lipoprotein deficiency	ABCA1	19	Homo sapiens (human)	Alliance of Genome Resources
DOID:13884	sick sinus syndrome Aliases: sinus node infection	AGT ANK2 HCN1 HCN4 SCN5A	10021 183 287 348980 6331	Homo sapiens (human)	Alliance of Genome Resources
DOID:1389	polyneuropathy	APOA4 FCGR3A HLA-DRB1 IL6 SERPINE1 SOD2 SOD3	2214 3123 337 3569 5054 6648 6649	Homo sapiens (human)	Alliance of Genome Resources
DOID:13891	bird fancier's lung Aliases: Avian hypersensitivity Pneumonitis Bird-fancier's lung Bird-fanciers' lung bird breeder's lung bird fancier lung pigeon breeder's lung poultry worker's lung	MUC1	4582	Homo sapiens (human)	Alliance of Genome Resources
DOID:1390	hypobetalipoproteinemia Aliases: Hypo-beta-lipoproteinemia	APOB APOC2 PCSK9	255738 338 344	Homo sapiens (human)	Alliance of Genome Resources
DOID:13909	red-green color blindness Aliases: Deutan defect Deuteranopia Reduced red-green discrimination	OPN1MW	2652	Homo sapiens (human)	Alliance of Genome Resources
DOID:1391	Norum disease Aliases: LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY lecithin acyltransferase deficiency	LCAT	3931	Homo sapiens (human)	Alliance of Genome Resources
DOID:13910	red color blindness Aliases: Protan defect Protanopia	OPN1LW	5956	Homo sapiens (human)	Alliance of Genome Resources
DOID:13922	eosinophilic esophagitis	CD40LG CYP2C19 PECAM1 TGFB1	1557 5175 7040 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:13929	lacrimal duct obstruction Aliases: Blocked lacrimal canaliculus Obstruction of lacrimal canaliculus Obstruction of lacrimal ducts	IGSF3	3321	Homo sapiens (human)	Alliance of Genome Resources
DOID:13934	facial paralysis Aliases: Facial Palsy	TUBB1 TUBB2A TUBB2B TUBB3 TUBB4A TUBB4B TUBB6 TUBB	10381 10382 10383 203068 347733 7280 81027 84617	Homo sapiens (human)	Alliance of Genome Resources
DOID:13938	amenorrhea Aliases: absence of menstruation amenia	FSHB	2488	Homo sapiens (human)	Alliance of Genome Resources
DOID:1394	urinary schistosomiasis Aliases: Schistosoma Hematobium Infection Schistosoma haematobium Schistosoma hematobium infectious disease Schistosomiasis due to schistosoma haematobium Schistosomiasis of bladder Vesical schistosomiasis bladder Schistosomiasis cystitis with bilharziasis	CD1D CTLA4 IL5 STAT6	1493 3567 6778 912	Homo sapiens (human)	Alliance of Genome Resources
DOID:13948	bladder neck obstruction Aliases: Obstruction of bladder neck or vesicourethral orifice	ADRA1A COL1A1 COL3A1 CYP19A1 ELN HIF1A HTR2A NGF NOS3 OPTN SOD2	10133 1277 1281 148 1588 2006 3091 3356 4803 4846 6648	Homo sapiens (human)	Alliance of Genome Resources
DOID:13949	interstitial cystitis Aliases: ulcerative cystitis	ADRB2 CSF1 CSF2 ERBB2 ERBB4 HIF1A MAPK14 MKI67 MTOR NGF NOS2 NRG1 VCAM1 VEGFA	1432 1435 1437 154 2064 2066 2475 3084 3091 4288 4803 4843 7412 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:1395	schistosomiasis	HLA-DRB1	3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:13963	nuclear senile cataract Aliases: Senile nuclear cataract Senile nuclear sclerosis	FTO	79068	Homo sapiens (human)	Alliance of Genome Resources
DOID:13976	peptic esophagitis Aliases: Peptic reflux disease Reflux oesophagitis reflux esophagitis	BMP4 CCL5 EGFR F11R IL13 IL5 PTGES TJP1 TNF	1956 3567 3596 50848 6352 652 7082 7124 9536	Homo sapiens (human)	Alliance of Genome Resources
DOID:13994	cleidocranial dysplasia Aliases: Marie-Sainton Disease cleidocranial dysostosis	RUNX2	860	Homo sapiens (human)	Alliance of Genome Resources
DOID:14004	thoracic aortic aneurysm	ACTA1 ACTA2 ACTB ACTBL2 ACTC1 ACTG1 ADAM10 ADAM17 COL1A1 COL6A3 CXCR3 FLNA LOX MFAP5 MMP12 MMP14 MMP1 MMP2 MMP8 MMP9 MYH11 MYLK PRKG1 SERPINE1 THSD4 TIMP1 TIMP3	102 1277 1293 2316 2833 345651 4015 4312 4313 4317 4318 4321 4323 4629 4638 5054 5592 58 59 60 6868 70 7076 7078 71 79875 8076	Homo sapiens (human)	Alliance of Genome Resources
DOID:14018	alcoholic liver cirrhosis Aliases: Alcoholic Cirrhosis Alcoholic cirrhosis of liver Laennec's cirrhosis Laennec's cirrhosis, alcoholic Portal cirrhosis	ALDH2 CYP2E1 DDR1 DDR2 GABRG2 IL18BP LEP MMP13 NR1D1 PLAU SERPINE1 SERPINF1 SOD2 TG TLR9	10068 1571 217 2566 3952 4322 4921 5054 5176 5328 54106 6648 7038 780 9572	Homo sapiens (human)	Alliance of Genome Resources
DOID:14021	Tietze's syndrome Aliases: Costalchondritis Costochondral junction syndrome Costochondritis Slipping rib syndrome Tietze's disease	MITF	4286	Homo sapiens (human)	Alliance of Genome Resources

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