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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 **4476 - 4500** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:384	Wolff-Parkinson-White syndrome Aliases: Anomalous A-V excitation Wolff-Parkinson-White pattern anomalous atrioventricular excitation	APRT ARSD B3GAT1 CNTN2 FCGR3B PRKAA2 PRKAG2 PRKAG3	2215 27087 353 414 51422 53632 5563 6900	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:13087	Lown-Ganong-Levine syndrome Aliases: atrial tachyarrhythmia with short PR interval syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias	APRT ARSD B3GAT1 CNTN2 FCGR3B PRKAA2	2215 27087 353 414 5563 6900	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:1035	aggressive NK-cell leukemia Aliases: aggressive NK-cell leukaemia large granular Lymphocyte Leukemia, NK-cell type natural killer cell leukaemia natural killer cell leukemia	B3GAT1 FCGR3B IL18R1 KLRB1 NCAM1 SOAT1 TP53 UGCG	2215 27087 3820 4684 6646 7157 7357 8809	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:7465	chronic NK-cell lymphocytosis Aliases: NK-cell large granular Lymphocyte Lymphocytosis	B3GAT1 FCGR3B KLRD1 NCAM1	2215 27087 3824 4684	Homo sapiens (human)	DisGeNET
DOID:13777	epidermodysplasia verruciformis	FCGR3B PTEN PTGS2 SCD SDCBP2 STS STT3A TM7SF2	2215 27111 3703 412 5728 5743 6319 7108	Homo sapiens (human)	DisGeNET
DOID:0060831	Griscelli syndrome Aliases: Chediak-Higashi-like syndrome Griscelli-Prunieras syndrome partial albinism-immunodeficiency syndrome	FCGR3B IDS	2215 3423	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0060218	CREST syndrome	CD22 FCGR3B MRC1	2215 4360 933	Homo sapiens (human)	DisGeNET
DOID:0090029	CINCA Syndrome Aliases: IOMID syndrome NOMID syndrome Prieur-Griscelli syndrome chronic infantile neurological cutaneous articular syndrome chronic neurologic cutaneous and articular syndrome cryopyrin-associated periodic syndrome 3 infantile-onset multisystem inflammatory disease neonatal-onset multisystem inflammatory disease	FCGR3B PLCG2 RPE	2215 5336 6120	Homo sapiens (human)	DisGeNET
DOID:9123	eczema herpeticum Aliases: Herpes simplex dermatitis of eyelid Herpes simplex eyelid dermatitis Herpes simplex virus dermatitis herpes simplex dermatitis herpes simplex virus eyelid dermatitis	CD14 FCGR3B	2215 929	Homo sapiens (human)	DisGeNET
DOID:624	transient hypogammaglobulinemia of infancy	FCGR3B	2215	Homo sapiens (human)	DisGeNET
DOID:0060771	obsolete dextro-looped transposition of the great arteries 1	CFC1 FKTN GPC3 HSPG2 PIGL	2218 2719 3339 55997 9487	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0060770	dextro-looped transposition of the great arteries Aliases: D-TGA DTGA1 congenitally uncorrected transposition of the great arteries congenitally uncorrected transposition of the great vessels isolated ventriculoarterial discordance ventriculoarterial discordance with atrioventricular concordance	CFC1 FKTN GPC3 HSPG2 PIGL	2218 2719 3339 55997 9487	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0112379	muscular dystrophy-dystroglycanopathy type B4 Aliases: MDDGB4 congenital muscular dystrophy FKTN-related	FKTN	2218	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080146	childhood B-cell acute lymphoblastic leukemia	CD22 CD38 FCN2 FUT4 LIPA MBL2 PIK3CA PIK3CB PIK3CG SLC2A5	2220 2526 3988 4153 5290 5291 5294 6518 933 952	Homo sapiens (human)	DisGeNET
DOID:0060592	B-cell adult acute lymphocytic leukemia Aliases: B-cell adult acute lymphocytic leukaemia adult B acute lymphoblastic leukaemia adult B acute lymphoblastic leukemia adult B-lymphoblastic leukaemia adult B-lymphoblastic leukemia adult b-cell acute lymphoblastic leukaemia adult b-cell acute lymphoblastic leukemia adult b-cell lymphocytic leukaemia adult b-cell lymphocytic leukemia	CD22 FCN2 FUT4 MBL2 PIK3CA PIK3CB PIK3CD PIK3CG PTEN	2220 2526 4153 5290 5291 5293 5294 5728 933	Homo sapiens (human)	DisGeNET
DOID:10456	tonsillitis Aliases: Throat infection - tonsillitis chronic tonsillitis	FCN2 GALNS GPX1 MBL2 NT5E	2220 2588 2876 4153 4907	Homo sapiens (human)	DisGeNET DisGeNET
DOID:8781	rubella Aliases: german measles	ABO CANX FCN2 HPGDS IL18R1 MRC1	2220 27306 28 4360 821 8809	Homo sapiens (human)	DisGeNET
DOID:1455	geographic tongue Aliases: Glossitis areata exfoliativa Pityriasis linguae benign migratory glossitis	FCN2 HPGDS PIK3CA PTEN SDHB SDHC SDHD	2220 27306 5290 5728 6390 6391 6392	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2755	Mycobacterium avium complex disease Aliases: Infection due to Mycobacterium intracellulare MAC disease Mycobacterium Avium Infection Mycobacterium avium Complex	ADIPOQ FCN2 ICAM1 NTM RGMA STS TNF	2220 3383 412 50863 56963 7124 9370	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:5078	ganglioglioma Aliases: CNS ganglioglioma adult ganglioglioma childhood ganglioglioma	FCN2 IDH1 IDH2 PIK3CA PIK3CD PIK3CG PTEN	2220 3417 3418 5290 5293 5294 5728	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0050145	adenoiditis Aliases: chronic adenoiditis	FCN2	2220	Homo sapiens (human)	DisGeNET
DOID:5691	visual cortex disease Aliases: visual cortex dysfunction	FDFT1 PIGP	2222 51227	Homo sapiens (human)	DisGeNET
DOID:5062	phencyclidine abuse Aliases: PCP abuse	FDFT1	2222	Homo sapiens (human)	DisGeNET
DOID:100	intestinal infectious disease Aliases: bacterial enteritis	APRT FDPS ICAM1 IL18R1 LCT LYZ PLA2G4A ST8SIA2	2224 3383 353 3938 4069 5321 8128 8809	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:3805	porokeratosis Aliases: disseminated superficial actinic porokeratosis	FDPS	2224	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources

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