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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 **3026 - 3050** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:10887	lepromatous leprosy Aliases: type L leprosy	C3 CD163 CFB HLA-DQA1 MBL2	3117 4153 629 718 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:10892	hypospadias Aliases: familial hypospadias	AR CYP1A1 FGF10 FGF8 FGFR2 FOS GLI3 HOXD13 HSD3B2 MAMLD1 SRD5A2	10046 1543 2253 2255 2263 2353 2737 3239 3284 367 6716	Homo sapiens (human)	Alliance of Genome Resources
DOID:10907	microcephaly Aliases: Microcephalus microencephaly	AARS1 AARS2 ASPM AUTS2 CARS1 CDK5RAP2 CHKA CHKB CIT COPB2 DHX37 EFTUD2 ETNK1 ETNK2 EXOC7 KATNB1 KIF20B MAPKBP1 MFSD2A NSD1 ODF2 PSMB1 PUS7 SLC25A19 TUBA1A TUBB WDR62	10300 11113 1119 1120 16 203068 23005 23265 259266 26053 284403 4957 54517 55224 55500 55755 5689 57505 57647 60386 64324 7846 833 84879 9276 9343 9585	Homo sapiens (human)	Alliance of Genome Resources
DOID:10908	hydrocephalus Aliases: hydrocephalus, X-linked hydrocephalus, nonsyndromic, autosomal recessive	ADD1 AQP1 AQP4 CCDC39 CCDC88C CELSR2 HMGB1 HSPD1 HYDIN ITGB1 KIF27 L1CAM MBOAT7 MPDZ NTF3 POMK PPARA SMARCC1 TMEM67	118 1952 3146 3329 339829 358 361 3688 3897 440193 4908 5465 54768 55582 6599 79143 84197 8777 91147	Homo sapiens (human)	Alliance of Genome Resources
DOID:10914	amnestic disorder Aliases: Amnestic syndrome Korsakoff's psychosis or syndrome amnesia	BCHE BDNF CREB1 DRD3 HRH3 HTR7 IRS1 IRS2 IRS4 MAPT	11255 1385 1814 3363 3667 4137 590 627 8471 8660	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:10930	borderline personality disorder	TPH1	7166	Homo sapiens (human)	Alliance of Genome Resources
DOID:10933	obsessive-compulsive disorder Aliases: Anancastic neurosis obsessive compulsive disorder	BDNF COMT CREB1 GDNF HRAS HTR2A SLC6A4	1312 1385 2668 3265 3356 627 6532	Homo sapiens (human)	Alliance of Genome Resources
DOID:10937	impulse control disorder	PRL	5617	Homo sapiens (human)	Alliance of Genome Resources
DOID:10939	antisocial personality disorder Aliases: Asocial personality Dissocial personality disorder Psychopath.personality Psychopathic personality Psychopathic personality disorder sociopathic personality	ABCB1 CACNG8 DRD4 HTR1B	1815 3351 5243 59283	Homo sapiens (human)	Alliance of Genome Resources
DOID:1094	attention deficit hyperactivity disorder Aliases: ADHD attention deficit disorder hyperkinetic disorder	ADGRE1 ADGRE5 ADGRL1 ADGRL2 ADGRL3 ADGRL4 ADRA2A AR BAIAP2 BDNF BRINP1 CALY CDH2 CHRNB2 COMT DBH DOCK3 DRD4 DRD5 FOXP2 GIT1 GRIN2B GRM8 HMGCR HTR1B LGALS3 MEF2A MEF2C MEF2D MMP9 NF1 NTRK2 PER1 PTCHD1 SLC6A2 SLC6A3 SLC6A4 SNAP25 TACR1 TPH1 UST VEGFA VPS4A	1000 10090 10458 1141 1312 139411 150 1620 1621 1795 1815 1816 2015 22859 23266 23284 27183 28964 2904 2918 3156 3351 367 3958 4205 4208 4209 4318 4763 4915 50632 5187 627 64123 6530 6531 6532 6616 6869 7166 7422 93986 976	Homo sapiens (human)	Alliance of Genome Resources
DOID:10941	intracranial aneurysm Aliases: brain aneurysm	AGER AOC3 ARHGEF17 CCL2 CCN1 COL1A2 COL22A1 CTSB CTSK CTSS EDN1 ENG IL6 KLF5 KMT2D MMP12 MMP14 MMP2 MMP9 NOS3 PKD1 PKD2 TIMP1 TNF VCAN VEGFA VWF	1278 1462 1508 1513 1520 169044 177 1906 2022 3491 3569 4313 4318 4321 4323 4846 5310 5311 6347 688 7076 7124 7422 7450 8085 8639 9828	Homo sapiens (human)	Alliance of Genome Resources
DOID:10952	nephritis	ACE AGTR1 CCL2 CXCR2 CYP2J2 EDN1 ICAM1 IFNG IL4 ITGA4 ITGAL ITGB2 NOS3 PARP1 PTK2 SERPINB7 SMAD6 SNRPD1	142 1573 1636 185 1906 3383 3458 3565 3579 3676 3683 3689 4091 4846 5747 6347 6632 8710	Homo sapiens (human)	Alliance of Genome Resources
DOID:10964	cholesteatoma of middle ear Aliases: Cholesteatoma of middle ear and mastoid Cholesteatoma of middle ear and/or mastoid Cholesteatoma of the middle ear Epidermosis of ear Epidermosis of middle ear middle ear cholesteatoma	HIF1A ICAM1 IL1A IL1R1 IL2 IL6 MMP1 MMP2 MMP9 RELA TLR2 TLR4 TNF TP53 VEGFA	3091 3383 3552 3554 3558 3569 4312 4313 4318 5970 7097 7099 7124 7157 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:10966	lipoid nephrosis Aliases: Minimal Change Glomerulonephritis Minimal change disease Nephrotic syndrome with lesion of minimal change glomerulonephritis Nephrotic syndrome with lesion of minimal change nephrotic syndrome	IL13 IL17A LGALS1 NR3C1 STAT6	2908 3596 3605 3956 6778	Homo sapiens (human)	Alliance of Genome Resources
DOID:10976	membranous glomerulonephritis Aliases: membranous nephropathy	A2M ABCA1 APOE C3 C7 CD40 CDKN1B CFB CFH HLA-DQA1 LRP2 LRPAP1 MME MMP9 NPHS1 NPHS2 NPNT PTGER3 PTPRU RHOA SHH SPARC TBXAS1 TF	10076 1027 19 2 255743 3075 3117 348 387 4036 4043 4311 4318 4868 5733 629 6469 6678 6916 7018 718 730 7827 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:1098	fetal erythroblastosis Aliases: EF - Erythroblastosis foetalis Haemolytic disease due to rhesus isoimmunisation erythroblastosis fetalis rhesus isoimmunisation of the newborn	FCGR2A	2212	Homo sapiens (human)	Alliance of Genome Resources
DOID:10983	Alport syndrome Aliases: Hereditary Nephritis	COL4A3 COL4A4 COL4A5 HLA-DRB1 MMP3	1285 1286 1287 3123 4314	Homo sapiens (human)	Alliance of Genome Resources
DOID:1099	alpha thalassemia Aliases: Alpha thalassaemia alpha-Thalassemia	GPX1 HBA1 HBA2 HBB HP	2876 3039 3040 3043 3240	Homo sapiens (human)	Alliance of Genome Resources
DOID:110	lens disease	ADAMTSL4	54507	Homo sapiens (human)	Alliance of Genome Resources
DOID:11030	corneal edema Aliases: Corneal oedema	IL1A	3552	Homo sapiens (human)	Alliance of Genome Resources
DOID:11044	gastroschisis	ADD1 IGF1R KIT LRP1 NOS2	118 3480 3815 4035 4843	Homo sapiens (human)	Alliance of Genome Resources
DOID:11049	meconium aspiration syndrome Aliases: Neonatal aspiration of meconium meconium aspiration	AGT AGTR2 ATF2	1386 183 186	Homo sapiens (human)	Alliance of Genome Resources
DOID:11054	urinary bladder cancer Aliases: bladder cancer tumor of the bladder	AKT1 ALOX12 AMACR APEX1 AREG BAX BRCA1 CA9 CASP9 CD44 CD82 CD9 CDC25A CDC25B CDH13 CDH1 CDKN1B CHEK2 COL6A3 COMT CTNNA1 CTNNB1 CTSB CXCR2 CYP1A1 CYP1B1 CYP2C9 DNMT1 E2F1 EEF1E1 EGFR ENO2 ERBB2 ERBB3 ERBB4 EZH2 F2 FAS FASLG FGFR2 FGFR3 FN1 HK1 HRAS HSPA1A ICAM1 IFNG IGFBP3 IL1RN IL2 JUP KDM5B KDR KIT KRAS KRT5 MAP2K4 MDM2 MGMT MKI67 MLH1 MMP13 MMP1 MMP2 MMP9 MRE11 MSH2 MSH6 MTR MUC1 MUC5B MYC NCSTN NME1 NME2 NOS3 PHB1 PLAU PLK1 PPARG PRKCA PTEN PTGS2 RB1 RELA RHOA RUNX3 SERPINE1 SFN SLC11A1 SMAD4 SOD2 SPARC SPP1 TERT TFF1 TGFBR1 THBS1 TIMP3 TLR2 TMEFF2 TNFRSF10A TOP2A TP53 TYMP TYMS VEGFA VEGFC VEGFD WIF1 WNT7B XRCC1	1012 1027 10765 11197 11200 1293 1312 1495 1499 1508 1543 1545 1559 1786 1869 1890 1956 2026 2064 2065 2066 207 2146 2147 2261 2263 2277 2335 23385 23600 23671 239 2810 2956 3098 3265 328 3303 3383 3458 3486 355 3557 3558 356 3579 3728 3732 374 3791 3815 3845 3852 387 4089 4193 4255 4288 4292 4312 4313 4318 4322 4361 4436 4548 4582 4609 4830 4831 4846 5054 5245 5328 5347 5468 5578 5728 5743 581 5925 5970 6416 6556 6648 6678 6696 672 7015 7031 7046 7057 7078 7097 7153 7157 727897 7298 7422 7424 7477 7515 768 842 864 8797 928 9521 960 993 994 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:1107	esophageal carcinoma Aliases: cancer of esophagus cancer of oesophagus carcinoma of esophagus carcinoma of oesophagus	GRB7 SLC7A5 STAT3	2886 6774 8140	Homo sapiens (human)	Alliance of Genome Resources

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