GlyCosmos Portal

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

Displaying entries **3101 - 3125** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	IFNG TLR2 TLR4	3458 7097 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:11512	Budd-Chiari syndrome Aliases: hepatic vein thrombosis	APOA1 F5	2153 335	Homo sapiens (human)	Alliance of Genome Resources
DOID:11516	hypertensive heart disease	NPPB	4879	Homo sapiens (human)	Alliance of Genome Resources
DOID:11520	benign hypertensive renal disease Aliases: hypertensive renal disease, benign hypertensive renal disease, benign, without mention of renal failure	MAP3K7	6885	Homo sapiens (human)	Alliance of Genome Resources
DOID:11555	Fuchs' endothelial dystrophy Aliases: FCED Fuchs' corneal dystrophy Fuchs' endothelial corneal dystrophy	AGBL1 C3 CLU COL8A2 LOXHD1 SLC4A11 TCF4 ZEB1	1191 123624 125336 1296 6925 6935 718 83959	Homo sapiens (human)	Alliance of Genome Resources
DOID:11563	retinal vasculitis	HLA-B	3106	Homo sapiens (human)	Alliance of Genome Resources
DOID:11569	neurocirculatory asthenia Aliases: Cardiovascular malfunction arising from mental factors Cardiovascular neurosis Da Costa's syndrome Krishaber's disease	SLC6A2	6530	Homo sapiens (human)	Alliance of Genome Resources
DOID:11573	listeriosis Aliases: Infection by Listeria monocytogenes Listeria infection	IL15 IL1RN	3557 3600	Homo sapiens (human)	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	ADIPOQ ADRA1A ADRA1B ADRA1D ADRB2 ADRB3 AKR1C3 AKT2 AMH AR ATP5F1B CAPN10 CD36 COMT CYP17A1 CYP19A1 CYP1A1 FST GPX3 HSD17B7 HSD3B1 HSD3B2 MMP2 NCOA2 NCOA4 NCOR1 NGFR NR3C1 NR3C2 PECAM1 PGR RARRES2 SERPINE1 VEGFA	10468 10499 11132 1312 146 147 148 154 1543 155 1586 1588 208 268 2878 2908 3283 3284 367 4306 4313 4804 5054 506 51478 5175 5241 5919 7422 8031 8644 9370 948 9611	Homo sapiens (human)	Alliance of Genome Resources
DOID:11613	hyperandrogenism Aliases: hyperandrogenization syndrome	IL6ST POMC PPARG	3572 5443 5468	Homo sapiens (human)	Alliance of Genome Resources
DOID:11624	penile benign neoplasm Aliases: Penile tumor neoplasm of penis	PTGES TOP2A	7153 9536	Homo sapiens (human)	Alliance of Genome Resources
DOID:11633	thyroid hormone resistance syndrome Aliases: Generalized thyroid hormone resistance Refetoff syndrome Thyroid hormone responsiveness defect thyroid hormone resistance	NCOA1 THRA	7067 8648	Homo sapiens (human)	Alliance of Genome Resources
DOID:11650	bronchopulmonary dysplasia Aliases: Bronchopulmonary dysplasia of newborn Chronic lung disease of prematurity Neonatal chronic lung disease Perinatal bronchopulmonary dysplasia Respiratory insufficiency neonatal chronic respiratory disease	BAX CASP9 CAT CD209 CHI3L1 DAG1 EDN1 EPAS1 FLT1 HIF1A IL1RN MBL2 MIF MUC1 SERPINE1 SFTPA1 SFTPB SFTPD TNF TP53	1116 1605 1906 2034 2321 30835 3091 3557 4153 4282 4582 5054 581 6439 6441 653509 7124 7157 842 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:11656	cicatricial pemphigoid Aliases: Cicatricial pemphigoid with ocular involvement Ocular pemphigoid benign mucous membrane pemphigoid benign mucous membrane pemphigoid with ocular involvement ocular pemphigus	CLU HLA-DQB1 HLA-DRB1 IL1RN TNF	1191 3119 3123 3557 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:11664	nephrosclerosis Aliases: renal sclerosis	ADRB1 PTGDS	153 5730	Homo sapiens (human)	Alliance of Genome Resources
DOID:11678	onchocerciasis Aliases: Infection by Onchocerca volvulus Onchocerca volvulus infection volvulosis	HLA-DPA1 HLA-DQA1 IL13	3113 3117 3596	Homo sapiens (human)	Alliance of Genome Resources
DOID:1168	familial hyperlipidemia Aliases: familial hyperlipoproteinemia hyperlipemia	ABCA1 ABCB1 ABCG8 ADIPOQ ALB APOB APOC2 APOE BCHE CCL2 CD40LG CYP2E1 F3 F7 GFPT1 HSD11B1 HSPA1B ITGAM KL LCAT LDLR LEP LIPC LPL MMP9 NOS3 RGN SDC1 SERPINC1 SERPINF2 SHC1 SMARCD1 TFPI TGFB1 VCAM1	1571 19 213 2152 2155 2673 3290 3304 338 344 348 3684 3931 3949 3952 3990 4023 4318 462 4846 5243 5345 590 6347 6382 64241 6464 6602 7035 7040 7412 9104 9365 9370 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:11695	portal vein thrombosis	F2 IGF1R SERPINE1	2147 3480 5054	Homo sapiens (human)	Alliance of Genome Resources
DOID:11702	dysgammaglobulinemia	CD40LG UNG	7374 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:1171	hyperlipoproteinemia type V Aliases: Fredrickson type V lipaemia familial hyperlipoproteinemia type V familial type 5 hyperlipoproteinemia	APOA5	116519	Homo sapiens (human)	Alliance of Genome Resources
DOID:11712	lipoatrophic diabetes mellitus Aliases: lipoatrophic diabetes	LMNA	4000	Homo sapiens (human)	Alliance of Genome Resources
DOID:11713	diabetic angiopathy Aliases: Diabetic vascular disorder diabetic peripheral angiopathy	BDKRB1 CCL2 CD28 CD40LG EPO F3 FAS FASLG FN1 GP1BA GPX1 HLA-DRB1 ICAM1 IL1RN ITGAM MMP14 NOS2 NOS3 PLAT PON1 RBP4 SERPINE1 SOD1 SOD2 SPARC TNF VEGFA	2056 2152 2335 2811 2876 3123 3383 355 3557 356 3684 4323 4843 4846 5054 5327 5444 5950 623 6347 6647 6648 6678 7124 7422 940 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:11714	gestational diabetes Aliases: GDM Gestational diabetes mellitus Maternal gestational diabetes mellitus	ADIPOQ AHSG ANGPTL6 APOD ATP2B4 CALB1 CCL2 CDKAL1 CYP24A1 CYP27B1 CYP2R1 DCN DNAH8 GAD2 GCK GGT1 GPX1 HNF1A ICAM1 IGF1R IL10 IL6 INHBA INS INSR ITPR1 ITPR2 ITPR3 LEP MET OGG1 PLAT RBP4 RYR1 RYR2 RYR3 SRRM1 TRPV5 TRPV6	10250 120227 1591 1594 1634 1769 197 2572 2645 2678 2876 3383 347 3480 3569 3586 3624 3630 3643 3708 3709 3710 3952 4233 493 4968 5327 54901 55503 56302 5950 6261 6262 6263 6347 6927 793 83854 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:11716	prediabetes syndrome Aliases: Prediabetes impaired glucose tolerance prediabetic state	AGT CALCA CCR2 GCG HLA-DRA IL6 KCNJ11 PPARGC1A PTPRN2 RELB SIRT3 SLC4A2 SLC4A8 UCP3	10891 183 23410 2641 3122 3569 3767 5799 5971 6522 729230 7352 796 9498	Homo sapiens (human)	Alliance of Genome Resources
DOID:11717	neonatal diabetes Aliases: diabetes mellitus syndrome in newborn infant neonatal diabetes mellitus	GCK HK2 HK3 HKDC1 INS	2645 3099 3101 3630 80201	Homo sapiens (human)	Alliance of Genome Resources

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