GlyCosmos Portal

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

Displaying entries **851 - 875** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:687	hepatoblastoma	APOA1 CDH1 CLDN1 CTNNB1 DPEP1 FAS GPC3 MKI67 SALL1 SALL4 SMO SPOP ZFHX3	1499 1800 2719 335 355 4288 463 57167 6299 6608 8405 9076 999	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:0080958	primary hypoalphalipoproteinemia 2 Aliases: Apolipoprotein A-I deficiency	APOA1	335	Homo sapiens (human)	Alliance of Genome Resources
DOID:12842	Guillain-Barre syndrome Aliases: Infectious neuronitis Post-infectious polyneuritis Postinfectious polyneuritis acute infective polyneuritis acute inflammatory demyelinating polyradiculopathy acute postinfectious polyneuropathy	APOA4 CCL2 CD86 CTSB GDNF PMP22	1508 2668 337 5376 6347 942	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:705	Leber hereditary optic neuropathy Aliases: Leber's hereditary optic neuropathy Leber's optic atrophy	APOA4 ND3 ND5 SOD2 TP53	337 4537 4540 6648 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:1172	hyperlipoproteinemia type IV Aliases: Endogenous hyperlipidaemia Fredrickson type IV Lipidemia Fredrickson type IV hyperlipoproteinemia Fredrickson type IV lipidaemia VLDL hyperlipoproteinemia familial hypertriglyceridemia	APOA5 APOC2	116519 344	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:0111421	familial apolipoprotein A5 deficiency Aliases: familial APOA5 deficiency familial apolipoprotein A-V deficiency	APOA5	116519	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: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:4606	bile duct cancer Aliases: Ca extrahepatic bile ducts bile duct tumor malignant neoplasm of the extrahepatic bile duct	APOB APOE TJP1	338 348 7082	Homo sapiens (human)	Alliance of Genome Resources
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia	APOB BCL11A C3 CD36 CD40LG CFB CYP2C19 F2 F3 GPX1 HBB HK1 HLA-DQB1 NOS3 NPPB PECAM1 PGF PON1 SPTA1 TGFB1 TNF	1557 2147 2152 2876 3043 3098 3119 338 4846 4879 5175 5228 53335 5444 629 6708 7040 7124 718 948 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:4607	biliary tract cancer Aliases: malignant tumour of biliary tract	APOB CYP1A1 PPARD	1543 338 5467	Homo sapiens (human)	Alliance of Genome Resources
DOID:4608	common bile duct neoplasm Aliases: neoplasm of common bile duct	APOB FSCN1 MSLN MTAP MUC1 MUC4 MUC5AC TYMP	10232 1890 338 4507 4582 4585 4586 6624	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111062	familial hypobetalipoproteinemia 1 Aliases: FHBL1	APOB	338	Homo sapiens (human)	Alliance of Genome Resources
DOID:3146	lipid metabolism disorder Aliases: dyslipidemia fatty acid metabolism disorder	APOC2 CPT1A CPT2 DHCR24 FADS2 HADHA HADHB HSD17B4 LEP LPIN1 LPIN2 LPIN3 MAT2A MVK NPY5R PPARA	1374 1376 1718 23175 3030 3032 3295 344 3952 4144 4598 4889 5465 64900 9415 9663	Homo sapiens (human)	Alliance of Genome Resources
DOID:14118	familial lipoprotein lipase deficiency Aliases: Fredrickson type I hyperlipoproteinemia Fredrickson type I lipaemia familial LPL deficiency familial hyperlipoproteinemia type I hypercholesterinaemic xanthomatosis hyperchylomicronemia mixed hyperglyceridemia	APOC2 LPL	344 4023	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111418	familial apolipoprotein C-II deficiency Aliases: C-II anapolipoproteinemia familial APOC2 deficiency familial apoC-II deficiency hyperlipoproteinemia, type 1b hyperlipoproteinemia, type Ib	APOC2	344	Homo sapiens (human)	Alliance of Genome Resources
DOID:3145	hyperlipoproteinemia type III Aliases: Remnant hyperlipidemia carbohydrate induced hyperlipemia familial hypercholesterolaemia with hyperlipaemia familial type 3 hyperlipoproteinemia	APOC3 APOE	345 348	Homo sapiens (human)	Alliance of Genome Resources
DOID:1561	cognitive disorder Aliases: cognitive disease	APOC3 APP BDNF CHRFAM7A CHRNA7 COMT CSF3 DBN1 DMD EPHB2 GRIN1 GRIN2A GRIN2B HTR7 IL4 IRAK1 LAMP2 MAPT MMP3 MMP9 PPARG	1139 1312 1440 1627 1756 2048 2902 2903 2904 3363 345 351 3565 3654 3920 4137 4314 4318 5468 627 89832	Homo sapiens (human)	Alliance of Genome Resources
DOID:10603	glucose intolerance Aliases: Glucose malabsorption Malabsorption of glucose	APOC3 CCL5 COQ2 HLA-DQA1 HNF1A HSPD1 LEP LEPR PON1 WFS1	27235 3117 3329 345 3952 3953 5444 6352 6927 7466	Homo sapiens (human)	Alliance of Genome Resources
DOID:2972	renal artery obstruction	APOC3 CD40 SOD1	345 6647 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111370	apolipoprotein C-III deficiency Aliases: HALP2 hyperalphalipoproteinemia 2	APOC3	345	Homo sapiens (human)	Alliance of Genome Resources
DOID:332	amyotrophic lateral sclerosis Aliases: ALS Lou Gehrig's disease motor neuron disease, bulbar	APOE AQP4 ATP13A2 ATP13A3 ATP13A5 BPTF C3 C5AR1 C9orf72 CASP9 CCR2 CHMP2B DCTN1 DPP6 EIF2AK2 EPG5 EPO EWSR1 FUS GDNF GOT1 GRN GSK3A GSK3B HDAC4 HMGB1 IGF1R IGF2R ITIH4 ITPR2 KDR KEAP1 KIF1B LCN2 LRRK2 MAP4 MAPT MMP1 MMP2 MMP9 MSTN NEFH NEFL NEFM NFE2L2 NRG1 OPTN PGF PON2 PON3 PPARGC1A PSMC4 PSMC5 PTGS2 PTPRZ1 SARM1 SERPINF1 SLC11A2 SLC1A2 SOD1 SOD3 SQSTM1 TARDBP TFAM UBQLN1 UBQLN2 UBQLN3 UBQLN4 UNC13A VAPA VAPB VEGFA ZNF106	10133 10891 120892 1639 1804 203228 2056 2130 2186 23025 23095 23098 23400 23435 2521 25978 2660 2668 2805 2896 2931 2932 29978 29979 3084 3146 344905 348 3480 3482 361 3700 3709 3791 3934 4134 4137 4312 4313 4318 4741 4744 4747 4780 4891 50613 5176 5228 5445 5446 5610 56893 5704 5705 5743 57724 5803 64397 6506 6647 6649 7019 718 728 729230 7422 79572 842 8878 9217 9218 9759 9817	Homo sapiens (human)	Alliance of Genome Resources

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