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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 **3176 - 3200** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:12176	goiter Aliases: goitre	TEK TG	7010 7038	Homo sapiens (human)	Alliance of Genome Resources
DOID:12177	common variable immunodeficiency Aliases: CVID acquired agammaglobulinemia acquired hypogammaglobulinemia common variable agammaglobulinemia sporadic hypogammaglobulinemia	DCLRE1C FCGR2A HLA-DQB1 ICOS IL21R MBL2 NFKB2 PECAM1	2212 29851 3119 4153 4791 50615 5175 64421	Homo sapiens (human)	Alliance of Genome Resources
DOID:12185	otosclerosis	AGT BMP2 BMP4 COL1A1 HLA-B	1277 183 3106 650 652	Homo sapiens (human)	Alliance of Genome Resources
DOID:12205	dengue disease Aliases: Dengue Fever breakbone fever classic dengue	CD209 F2 FCGR2A GC IFNL1	2147 2212 2638 282618 30835	Homo sapiens (human)	Alliance of Genome Resources
DOID:12206	dengue hemorrhagic fever Aliases: DHF	CD1D CD209 FCGR2A IFNL1 IL21 KIR3DS1 SLC6A4	2212 282618 30835 3813 59067 6532 912	Homo sapiens (human)	Alliance of Genome Resources
DOID:12215	oligohydramnios Aliases: Oligohydramnios - delivered antepartum oligohydramnios delivered oligohydramnios	PDGFA PDGFB PDGFRA PDGFRB PDPN	10630 5154 5155 5156 5159	Homo sapiens (human)	Alliance of Genome Resources
DOID:12217	Lewy body dementia Aliases: Dementia with Lewy bodies Diffuse Lewy body disease Lewy body disease Senile dementia of the Lewy body type	ANXA5 APOE CCR1 CHRNA4 CHRNA7 ELK1 GBA1 GPR37 IGF1R IGF2 KLK6 MAP2 NEFL NGFR NOS2 PCNA SNCA SNCB SNCG TARDBP	1137 1139 1230 2002 23435 2629 2861 308 348 3480 3481 4133 4747 4804 4843 5111 5653 6620 6622 6623	Homo sapiens (human)	Alliance of Genome Resources
DOID:1222	cartilage disease Aliases: Cartilage disorder Chondropathy	BMP4 MMP3	4314 652	Homo sapiens (human)	Alliance of Genome Resources
DOID:12236	primary biliary cholangitis Aliases: biliary liver cirrhosis cholestatic cirrhosis chronic nonsuppurative destructive cholangitis primary biliary cirrhosis	ABCA1 ABCB4 ABCC2 ACE2 ACE AGT AQP4 CCL5 CCN2 CD14 CD68 COL1A1 CPEB1 CPEB4 CTLA4 DAG1 DNASE1 ENTPD2 FAS HHIP HLA-DQA1 IFNG IL10 IL12A IL12RB1 IL4 IL6 KRT18 LBR LEP LEPR MAS1 MMP13 MMP2 MMP3 MMP9 MUC2 NOS2 NOS3 NR3C1 NUP62 PDE5A PPARGC1A RELA REN RPS6KB1 SLCO1A2 SLCO1C1 SOD2 STAT4 TLR9 TNF UTP4 VEGFA	10891 1244 1277 1490 1493 1605 1636 1773 183 19 23636 2908 3117 3458 355 3565 3569 3586 3592 3594 361 3875 3930 3952 3953 4142 4313 4314 4318 4322 4583 4843 4846 5244 53919 54106 59272 5970 5972 6198 6352 64399 64506 6579 6648 6775 7124 7422 80315 84916 8654 929 954 968	Homo sapiens (human)	Alliance of Genome Resources
DOID:12241	beta thalassemia	APOB APOE BCL11A CFB COL1A1 HBB HBS1L HFE HLA-DQB1 HP IGFBP3 IL1A IL6 PON1 TERT TNF	10767 1277 3043 3077 3119 3240 338 348 3486 3552 3569 53335 5444 629 7015 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:12253	testicular lymphoma Aliases: lymphoma of the testis malignant lymphoma of testis	MYD88	4615	Homo sapiens (human)	Alliance of Genome Resources
DOID:12259	hemophilia B Aliases: Congenital factor IX deficiency Congenital factor IX disorder deficiency, functional factor IX factor IX deficiency	F2 F9	2147 2158	Homo sapiens (human)	Alliance of Genome Resources
DOID:1227	neutropenia	AP3B1 C5 C5AR1 CSF2 CSF3 CSF3R FCGR2A ITGAM MKI67 PTAFR SRP54 STAT2 STAT3 TNF	1437 1440 1441 2212 3684 4288 5724 6729 6773 6774 7124 727 728 8546	Homo sapiens (human)	Alliance of Genome Resources
DOID:12270	coloboma Aliases: coloboma of eye coloboma of macula congenital ocular coloboma	DZIP1 FZD5 LAMB1 PTCH2 SALL2 TMEM67 YAP1	10413 22873 3912 6297 7855 8643 91147	Homo sapiens (human)	Alliance of Genome Resources
DOID:12271	aniridia Aliases: Aplasia of iris isolated aniridia	ELP4	26610	Homo sapiens (human)	Alliance of Genome Resources
DOID:1229	paranoid schizophrenia Aliases: Paranoid type schizophrenia Paraphrenia - late Paraphrenic schizophrenia chronic paranoid schizophrenia paranoid type schizophrenia subchronic state	HSPA1A KCNN3	3303 3782	Homo sapiens (human)	Alliance of Genome Resources
DOID:12297	Vogt-Koyanagi-Harada disease Aliases: Harada's disease Vogt-Koyanagi syndrome uveomeningoencephalitic syndrome	HLA-DQA1 HLA-DQB1 HLA-DRB1 IFNG ITGB2 STAT4 TNF	3117 3119 3123 3458 3689 6775 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:12305	Bloch-Sulzberger syndrome Aliases: Incontinentia pigmenti Incontinentia pigmenti syndrome	NSDHL	50814	Homo sapiens (human)	Alliance of Genome Resources
DOID:12306	vitiligo	C4A CAT COMT CTLA4 ESR1 HGF HLA-DQA1 HLA-DQB1 HLA-DRB1 HSPA1A IFNG IL13 IL17A IL1A IL2 IL4 MBL2 NCSTN SOD2 TGFB1 TLR2 TLR4 TNF TYR	1312 1493 2099 23385 3082 3117 3119 3123 3303 3458 3552 3558 3565 3596 3605 4153 6648 7040 7097 7099 7124 720 7299 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:12308	Dubin-Johnson syndrome Aliases: Dubin Johnson syndrome chronic idiopathic jaundice	ABCC2 ABCC3 RDX SLCO1A2	1244 5962 6579 8714	Homo sapiens (human)	Alliance of Genome Resources
DOID:12336	male infertility	ADAMTS16 ARMC2 BSCL2 CABYR CAPZA3 CFAP47 CSNK2A2 CYLC1 FAS GPX3 KIT PMFBP1	1459 1538 170690 26256 26580 286464 2878 355 3815 83449 84071 93661	Homo sapiens (human)	Alliance of Genome Resources
DOID:12337	varicocele Aliases: Scrotal varices	CASP9 FAS HIF1A HSPD1 IL1A	3091 3329 355 3552 842	Homo sapiens (human)	Alliance of Genome Resources
DOID:12347	osteogenesis imperfecta Aliases: Lobstein's syndrome Osteopsathyrosis Vrolik's disease brittle bone disease	BMP1 CCDC134 COL1A1 COL1A2 PHLDB1 SMAD4 SMPD3	1277 1278 23187 4089 55512 649 79879	Homo sapiens (human)	Alliance of Genome Resources
DOID:12351	alcoholic hepatitis Aliases: acute alcoholic hepatitis acute alcoholic liver disease	ABCB11 AGT AHR ALB CCL2 CCL5 COL1A1 CPT1A CYP7A1 DDR1 FAS ICAM1 IL13 NFKB1 PPARA SLC10A1 SREBF1 TNF	1277 1374 1581 183 196 213 3383 355 3596 4790 5465 6347 6352 6554 6720 7124 780 8647	Homo sapiens (human)	Alliance of Genome Resources
DOID:12361	Graves' disease Aliases: Grave's disease Graves disease exophthalmic goiter	ADIPOQ ADRB2 BTNL2 C4A C4B CAT CD40 CD40LG CTLA4 CYP1A1 DNMT1 FAS GC HLA-B HLA-DQA1 HLA-DQB1 HLA-DRB1 HLA-DRB3 ICAM1 IFNG IGF1R IL10 IL13 IL17A IL23R IL2 IL3 IL6 IL6R ITGB3 LTA OGG1 SERPINE1 SLC25A16 TG TNF TP53 TSHR VEGFA	149233 1493 154 1543 1786 2638 3106 3117 3119 3123 3125 3383 3458 3480 355 3558 3562 3569 3570 3586 3596 3605 3690 4049 4968 5054 56244 7038 7124 7157 720 721 7253 7422 8034 847 9370 958 959	Homo sapiens (human)	Alliance of Genome Resources

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