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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 **1476 - 1500** of **4649** in total

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Disease ID	Disease Name ▲	Gene Symbol	Gene ID	Organism	Source
DOID:3689	brachial plexus neuritis Aliases: Brachial neuritis Parsonage-Aldren-Turner syndrome	SEPTIN9	10801	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070415	brachycephaly, trichomegaly, and developmental delay Aliases: BTDD MCINS Macinnes syndrome	RPS23	6228	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110964	brachydactyly type A1 Aliases: BDA1 Farabee type brachydactyly	GDF5 IHH	3549 8200	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110977	brachydactyly type A1C Aliases: BDA1C	GDF5	8200	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110978	brachydactyly type A1D Aliases: BDA1D	BMPR1B	658	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110965	brachydactyly type A2 Aliases: BDA2 Mohr-Wriedt type brachydactyly brachymesophalangy II	BMP2 BMPR1B CDK7 GDF5	1022 650 658 8200	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110967	brachydactyly type A4 Aliases: BDA4 Temtamy type brachydactyly brachymesophalangy II and V	HOXD13	3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110969	brachydactyly type B1 Aliases: BDB1	ROR2	4920	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110975	brachydactyly type B2 Aliases: BDB2	NOG	9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110970	brachydactyly type C Aliases: BDC	GDF5	8200	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110971	brachydactyly type D Aliases: BDD	HOXD13	3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110972	brachydactyly type E1 Aliases: BDE1	HOXD13	3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110976	brachydactyly type E2 Aliases: BDE2	PTHLH	5744	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050581	brachydactyly	HOXD13 SLC26A2	1836 3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050689	brachydactyly-syndactyly syndrome	HOXD13	3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome Aliases: DASS STHAG6 dental anomalies and short stature platyspondyly with amelogenesis imperfecta selective tooth agenesis 5	LTBP3	4054	Homo sapiens (human)	Alliance of Genome Resources
DOID:1319	brain cancer Aliases: BT - Brain tumour adult brain tumor adult malignant brain neoplasm brain neoplasm brain neoplasm, adult malignant brain tumour malignant primary brain neoplasm malignant primary brain tumor malignant tumor of Brain malignant tumor of adult brain neoplasm of brain primary brain neoplasm primary brain tumor primary malignant neoplasm of brain tumor of the Brain	AURKB HES1 L3MBTL1 L3MBTL4 LLGL1 LLGL2 MYC NOTCH1 NOTCH2 NOTCH3 NUMBL TERT VPS26A	26013 3280 3993 3996 4609 4851 4853 4854 7015 91133 9212 9253 9559	Homo sapiens (human)	Alliance of Genome Resources
DOID:11457	brain compression	CFL1	1072	Homo sapiens (human)	Alliance of Genome Resources
DOID:936	brain disease Aliases: encephalopathy	CD163 CPT2 DBR1 ENO2 MFF MYCBP2 NUP214 PTEN RANBP2 SLC6A4 STIM2 TJP1 UNC93B1	1376 2026 23077 51163 56947 5728 57620 5903 6532 7082 8021 81622 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:4724	brain edema Aliases: intracranial swelling wet brain	ABCC8 AQP1 AQP3 AQP4 AVPR1A C5 CACNA1B CP DMD F2 F2R GFAP ICAM1 KCNN4 MMP9 PLAT PLAU SCN3B SERPINE2 SERPINF1 SOD2 VEGFA	1356 1756 2147 2149 2670 3383 358 360 361 3783 4318 5176 5270 5327 5328 552 55800 6648 6833 727 7422 774	Homo sapiens (human)	Alliance of Genome Resources
DOID:3073	brain glioblastoma multiforme Aliases: Glioblastoma multiforme of brain brain Glioblastoma	EEF2 NCAM1	1938 4684	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060108	brain glioma Aliases: lower grade glioma	BAX FADD FAS FASLG FOXA1 GAPDH KDR PTPRB VEGFA XRCC1	2597 3169 355 356 3791 5787 581 7422 7515 8772	Homo sapiens (human)	Alliance of Genome Resources
DOID:3454	brain infarction	ADIPOQ ADM ADNP ALDH2 CACNA2D1 CALCRL CD8A CFH CTSB CYP11B1 CYP11B2 CYP2R1 GPNMB GZMB HGF HIF1A HLA-DQA1 HMGB1 HTR2B ICAM1 IGF2 IL15 IL2 KCNK6 MDK MMP14 MMP8 MMP9 MSI1 NES PARG PDGFB PRCP SCN7A TBXAS1 TNF TPCN2	10203 10457 10763 120227 133 1508 1584 1585 217 219931 23394 3002 3075 3082 3091 3117 3146 3357 3383 3481 3558 3600 4192 4317 4318 4323 4440 5155 5547 6332 6916 7124 781 8505 925 9370 9424	Homo sapiens (human)	Alliance of Genome Resources
DOID:2316	brain ischemia Aliases: Ischaemic encephalopathy Ischemic encephalopathy cerebral ischemia	ABCB1 ADAMTS1 AGER AKAP12 AKAP1 AKT1 ALOX15 ALOX5 ANGPT1 ANGPT2 ANXA1 APEX1 AQP3 AQP4 AQP5 AQP8 BAD BMP6 BTG2 C3 CASP6 CAST CAT CCL2 CCR5 CDK5 CLU CP CREB1 CSF2RB CSF3 CSPG4 CTSB CTSC CTSL CTSV DBH DPYSL2 DRD2 EDN1 EPOR F2R FAS FASLG FGA GAL GC GFRA1 GLUD1 GLUD2 HIF1A HSPA1B HSPA8 HSPA9 IL17A IL6ST IRAK1 IRAK4 ITGAM KCNK10 KCNK2 KDR LGALS3 LIF LONP1 MAP2 MAPT MDH2 MDK MMP13 MMP14 MMP2 MMP9 MSI1 NES NOS1 NOS3 NPPA NPTXR NR3C1 OPRM1 PAK1 PCNA PGF PLA2G4A PLAT PPP1R15A PRKACB PRKCA PROZ PTGIS PTGS1 PTGS2 RET SCN5A SELE SERPINE1 SLC11A2 SLC29A1 SLC6A1 SLC8A1 SLC8A2 SLC8A3 SOS1 SRC TEK TGFB1 TJP1 TLR4 TNFRSF1A TTR	1020 1075 10763 1191 1234 1356 1385 1439 1440 1464 1508 1514 1515 1621 177 1808 1813 1906 2030 2057 207 2149 2243 23467 23645 240 246 2638 2674 2746 2747 284 285 2908 301 3091 328 3304 3312 3313 343 355 356 3572 360 3605 361 362 3654 3684 3776 3791 3958 3976 4133 4137 4191 4192 4313 4318 4322 4323 4440 4842 4846 4878 4891 4988 5054 5058 51083 5111 51135 5228 5243 5321 5327 54207 5567 5578 572 5740 5742 5743 5979 6331 6347 6401 6529 654 6543 6546 6547 6654 6714 7010 7040 7082 7099 7132 718 7276 7832 8165 831 839 847 8858 9361 9510 9590	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090125	brain small vessel disease 1 Aliases: BSVD1 COL4A1-related brain small vessel disease with hemorrhage COL4A1-related familial vascular leukoencephalopathy COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy brain small vessel disease with Axenfeld-Riegar anomaly brain small vessel disease with hemorrhage brain small vessel disease with or without ocular anomalies infantile hemiparesis leukoencephalopathy with Axenfeld-Riegar anomaly	COL4A1	1282	Homo sapiens (human)	Alliance of Genome Resources

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