GlyCosmos Portal

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Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **301 - 325** of **4621** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:0060851	pemphigus vulgaris Aliases: familial pemphigus vulgaris	ACE CYP21A2 FCN2 MBL2 MRC1	1589 1636 2220 4153 4360	Homo sapiens (human)
DOID:0111230	congenital muscular dystrophy-dystroglycanopathy type A11 Aliases: MDDGA11 Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11	B3GALNT2	148789	Homo sapiens (human)
DOID:0060640	ethylmalonic encephalopathy	ALDH3A2 ANXA5	224 308	Homo sapiens (human)
DOID:5855	anteroseptal myocardial infarction	ACE CAT LGALS3 SLC2A4	1636 3958 6517 847	Homo sapiens (human)
DOID:0050495	exanthema subitum Aliases: Roseola Infantum Sixth Disease	ABO CANX CDS1 CYB5R3 FCN2 HPGDS IL18R1 MRC1	1040 1727 2220 27306 28 4360 821 8809	Homo sapiens (human)
DOID:2101	vulva squamous cell carcinoma Aliases: Vulvar Epidermoid carcinoma vulvar squamous cell carcinoma	CD44 PIK3CA	5290 960	Homo sapiens (human)
DOID:4916	pituitary carcinoma Aliases: carcinoma of the Pituitary gland	CD44 CDH13 HSD11B2 IDH1 IDH2 LDHA PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 PTEN PTGS2 SCP2 SMUG1 STS TBXAS1	1012 23583 3291 3417 3418 3939 412 5290 5291 5293 5294 5563 5728 5743 6342 6916 960	Homo sapiens (human)
DOID:0080507	Cornelia de Lange syndrome 3 Aliases: CDLS3 Cornelia De Lange syndrome 3 with or without midline brain defects	SMC3	9126	Homo sapiens (human)
DOID:0070034	autosomal dominant intellectual developmental disorder 4 Aliases: MRD4 autosomal dominant mental retardation 4 autosomal dominant non-syndromic intellectual disability 4	ST3GAL4	6484	Homo sapiens (human)
DOID:204	enthesopathy	ACLY ADH1B CALR CD14 CD22 CD44 ENPP1 FMOD FOLR2 HSPG2 KL KLRC1 KLRD1 LGALS8 NT5E PTGS2 SELL VCAM1	125 2331 2350 3339 3821 3824 3964 47 4907 5167 5743 6402 7412 811 929 933 9365 960	Homo sapiens (human)
DOID:11830	myopia Aliases: near vision near-sightedness short-sightedness	ACOX1 ACSL4 AGK ALDH3A2 ATP6V0A2 B3GALNT2 B3GALT6 B3GLCT CHST14 COL9A2 DAG1 DCN ENPP1 FKRP FKTN FMOD GLUL GMPPB GNPTG GPAA1 GPD2 HADHA HAS2 HS6ST2 HSPG2 LARGE1 LPIN2 NTM NYX PCYT1A PIK3CA PIK3CG PLOD3 PMM2 POMGNT1 POMK POMT1 POMT2 PSMD10 PTEN PXYLP1 RPE SDHC SDHD SLC2A10 SMC3 TMTC3 VCAN XYLT1 XYLT2	10585 113189 126792 1298 145173 1462 148789 160418 1605 1634 2182 2218 224 2331 23545 2752 2820 29925 29954 3030 3037 3339 50863 51 5130 5167 5290 5294 5373 55624 55750 5716 5728 60506 6120 6391 6392 64131 64132 79147 81031 84197 84572 8733 8985 90161 9126 9215 92370 9663	Homo sapiens (human)
DOID:10939	antisocial personality disorder Aliases: Asocial personality Dissocial personality disorder Psychopath.personality Psychopathic personality Psychopathic personality disorder sociopathic personality	ACE ADH1B ALDH2 CAT COMT CYP2E1 EXT1 GAD1 IMPA1	125 1312 1571 1636 2131 217 2571 3612 847	Homo sapiens (human)
DOID:437	myasthenia gravis	ACHE APRT B3GAT1 CD55 CDIPT CDS1 CLC CNTFR CYP21A2 CYP3A5 IL18R1 LGALS1 LGALS8 NCAM1	1040 10423 1178 1271 1577 1589 1604 27087 353 3956 3964 43 4684 8809	Homo sapiens (human)
DOID:0110558	autosomal dominant nonsyndromic deafness 2A Aliases: DFNA2A autosomal dominant deafness 2A	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:9487	Meckel's diverticulum Aliases: Meckel Diverticulum Persistent vitelline duct	ACSL4 ALG13 GPC3 IL1RAPL1	11141 2182 2719 79868	Homo sapiens (human)
DOID:9766	xanthogranulomatous cholecystitis	CEACAM5	1048	Homo sapiens (human)
DOID:0050463	campomelic dysplasia Aliases: Acampomelic Campomelic Dysplasia	ACE ALPL B4GALNT2 CD177 CHKB DAG1 FKRP FKTN IGF2R LGALS4 MPI POMT1 POMT2 ST3GAL4	10585 1120 124872 1605 1636 2218 249 29954 3482 3960 4351 57126 6484 79147	Homo sapiens (human)
DOID:600	animal phobia Aliases: Fear of animals Zoophobia	CAT DDOST	1650 847	Homo sapiens (human)
DOID:0050854	Muckle-Wells syndrome Aliases: MWS neutrophilic urticaria	IL18R1 NT5E PLCG2	4907 5336 8809	Homo sapiens (human)
DOID:0110133	Bardet-Biedl syndrome 11 Aliases: BBS11	INPP5E PIGX	54965 56623	Homo sapiens (human)
DOID:2773	contact dermatitis Aliases: Contact dermatitis/eczema Contact eczema Dermatitis, venenata dermatitis venenata	AKR1B10 AKR1C2 CD44 CYP1A1 CYP1B1 G6PD GLB1 UGT1A1 UGT1A6	1543 1545 1646 2539 2720 54578 54658 57016 960	Homo sapiens (human)
DOID:0110629	Wolfram syndrome 1 Aliases: DIDMOAD WFS1 diabetes mellitus AND insipidus with optic atrophy AND deafness	COMT	1312	Homo sapiens (human)
DOID:10824	malignant hypertension	ACE CYP17A1 CYP1A1 SLC33A1	1543 1586 1636 9197	Homo sapiens (human)
DOID:1508	candidiasis Aliases: Disseminated candidiasis systemic candidiasis	ADH1A AKR1A1 CLEC6A CLEC7A CYP51A1 ENO1 FUT2 FUT3 FUT4 FUT5 FUT6 FUT7 FUT9 INPP5D LGALS3 LYZ MBL2 PLB1 PLCG1 PLCG2 PLD1 PSAP SRGN TMEM199	10327 10690 124 147007 151056 1595 2023 2524 2525 2526 2527 2528 2529 3635 3958 4069 4153 5335 5336 5337 5552 5660 64581 93978	Homo sapiens (human)
DOID:13141	uveitis	ACAN ACE AKR1B1 CD14 CYP24A1 CYP27B1 EXTL3 ICAM1 IL1RAP MICA OVGP1 PIK3CA PIK3CB PIK3CG PLA2G15 RPE RTN4R SMUG1 TLR4 TM7SF2 TNF VCAN VTCN1	100507436 1462 1591 1594 1636 176 2137 231 23583 23659 3383 3556 5016 5290 5291 5294 6120 65078 7099 7108 7124 79679 929	Homo sapiens (human)

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