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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5776 - 5800** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:327	syringomyelia	CD38 CNTN2 CYP2U1 ERLEC1 GNPTAB HPRT1 IL18RAP PTGS2 SMUG1 TMTC1	113612 23583 27248 3251 5743 6900 79158 83857 8807 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:5612	spinal cancer Aliases: Intraspinal tumor malignant tumor of the Spinal Cord spinal cord cancer spinal cord neoplasm tumor of the Spinal Cord	ACSS2 ARSA PLA2G15 SMUG1 TREH	11181 23583 23659 410 55902	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:672	spleen cancer Aliases: Splenic neoplasm malignant Splenic tumor malignant tumour of spleen spleen neoplasm	CEACAM5	1048	Homo sapiens (human)	DisGeNET
DOID:1123	spondyloarthropathy Aliases: spondarthropathy spondylarthrosis	ACAN ACE ALDOA CD14 CD74 CYP17A1 ENO1 ENPP1 FCGR3B KL KLRB1 KLRK1 MBL2 MICA PTGS2 SFTPA2 SMUG1 SOAT1 TNF VCAN	100507436 1462 1586 1636 176 2023 2215 226 22914 23583 3820 4153 5167 5743 6646 7124 729238 929 9365 972	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:6590	spondylitis	ACAN MICA SMUG1 VCAN	100507436 1462 176 23583	Homo sapiens (human)	DisGeNET
DOID:7147	ankylosing spondylitis Aliases: Bekhterev syndrome Bekhterev's disease Marie-Strumpell disease	ACE ADIPOQ ALPL ALPP ARSA ATRNL1 CAT CD14 CD38 CD74 CLEC16A CYP1A1 CYP1B1 CYP24A1 CYP2C9 CYP3A5 DAG1 DLAT DPEP1 ENPP1 FCGR3B FUT2 GAL3ST2 IL18R1 IL1R1 LGALS3 LSS MBL2 MICA NT5E PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGIS PTGS2 SCD5 SELP SFTPA2 SGSH SIGLEC7 SOAT1 ST8SIA4 SULT1E1 TLR4 UGT2B17 UST	100507436 10090 1543 1545 1559 1577 1591 1605 1636 1737 1800 2215 23274 249 250 2524 26033 27036 3554 3958 4047 410 4153 4907 5167 5290 5291 5293 5294 5728 5740 5743 6403 64090 6448 6646 6783 7099 729238 7367 7903 79966 847 8809 929 9370 952 972	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda	ACAN CD38 CHST3 GLB1 HSPG2	176 2720 3339 9469 952	Homo sapiens (human)	DisGeNET DisGeNET
DOID:10426	Klippel-Feil syndrome Aliases: Klippel-Feil and Turner syndrome Klippel-Feil deformity, deafness and facial asymmetry autosomal dominant Klippel-Feil syndrome congenital dystrophia brevicollis congenital synostosis of cervical vertebrae	ACSS2 AGA B3GLCT CD38 COLEC10 COLEC11 EBP IDUA INPP5E LFNG MAN2B1 MASP1 PLA2G15	10584 10682 145173 175 23659 3425 3955 4125 55902 5648 56623 78989 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:6682	spondylolisthesis	ACSS2 AGA B3GLCT CD38 COLEC10 COLEC11 EBP IDUA INPP5E LFNG MAN2B1 MASP1 PLA2G15	10584 10682 145173 175 23659 3425 3955 4125 55902 5648 56623 78989 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2300	spondylolysis	AGA SLC26A2	175 1836	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:2247	spondylosis Aliases: Lumbar spondylosis with myelopathy Spondylogenic compression of lumbar spinal cord Spondylogenic compression of thoracic spinal cord Thoracic or lumbar spondylosis with myelopathy lumbosacral spondylosis without myelopathy spondylosis with myelopathy	ACAN ACE ALDOA CD14 CD74 CYP17A1 ENO1 ENPP1 FCGR3B KL KLRB1 KLRK1 MBL2 MICA PTGS2 SFTPA2 SOAT1 VCAN	100507436 1462 1586 1636 176 2023 2215 226 22914 3820 4153 5167 5743 6646 729238 929 9365 972	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:6603	Kummell's disease Aliases: Kummell disease Kummell's spondylitis Traumatic spondylopathy	KL	9365	Homo sapiens (human)	DisGeNET
DOID:11103	rickettsialpox Aliases: Rickettsia akari spotted fever Vesicular rickettsiosis	CS	1431	Homo sapiens (human)	DisGeNET
DOID:11104	spotted fever Aliases: Spotted fever group rickettsial disease	CS	1431	Homo sapiens (human)	DisGeNET
DOID:10921	Siberian tick typhus Aliases: North Asian tick fever North Asian tick typhus Rickettsia sibirica spotted fever manchurian typhus	CS	1431	Homo sapiens (human)	DisGeNET
DOID:96	staphyloenterotoxemia Aliases: Staphylococcal food poisoning Staphylococcal toxaemia due to food staphyloenterotoxicosis	SFTPA1	653509	Homo sapiens (human)	DisGeNET
DOID:9063	Ritter's disease Aliases: Dermatitis exfoliativa neonatorum Pemphigus neonatorum Ritter disease Scalded skin syndrome Staphylococcal scalded skin syndrome Toxic epidermal necrolysis, subcorneal type	EXT1	2131	Homo sapiens (human)	DisGeNET
DOID:9362	status asthmaticus Aliases: Asthma with status asthmaticus Severe asthma attack	CD14	929	Homo sapiens (human)	DisGeNET
DOID:1824	status epilepticus Aliases: Grand mal status	ABAT ACAN ACHE ALDH5A1 ALDH7A1 AMACR APEX1 APOD ATP6V0A2 ATP6V1A CAT CD33 CD44 COG8 CPT2 CYP11A1 CYP19A1 DHCR24 DHDDS EPM2A FH FIG4 FUT2 GALC GAPDH GPAA1 GSK3B HSD11B1 IDH1 IDH2 IL6ST KCNJ11 MGLL NT5E OGDH OGG1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLAUR PTEN PTGES PTGS2 ST3GAL5 SYNJ1 TMED9 TNF UGCG UGT1A1 UGT1A6 UGT1A7	11343 1376 142 1583 1588 1718 176 18 2271 23545 23600 2524 2581 2597 2932 328 3290 3417 3418 347 3572 3767 43 4907 4967 4968 501 523 5290 5291 5293 5294 5321 5329 54577 54578 54658 54732 5728 5743 7124 7357 7915 7957 79947 84342 847 8733 8867 8869 945 9536 960 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:10602	obsolete steatorrhea	ACOX2 BAAT CYP7B1 HSD3B7 LIPA PNLIP	3988 5406 570 80270 8309 9420	Homo sapiens (human)	DisGeNET
DOID:2303	stereotypic movement disorder Aliases: Stereotyped repetitive movements Stereotypy habit disorder	B3GALNT2 CHAT EXT2 GAD1 HGSNAT LMAN2L MAN1B1 MBOAT7 MGAT2 NDST1 OCRL PGAP1 PIGC ST3GAL3 ST3GAL5 TECR TKT TUSC3	1103 11253 138050 148789 2132 2571 3340 4247 4952 5279 6487 7086 79143 7991 80055 81562 8869 9524	Homo sapiens (human)	DisGeNET
DOID:4072	duodenum disease Aliases: duodenal disease duodenum disorder	CAT CEACAM5 CEACAM7 CYP2C9 DHRS11 HSD17B7 OGG1 PTEN PTGS2	1048 1087 1559 4968 51478 5728 5743 79154 847	Homo sapiens (human)	DisGeNET
DOID:10808	gastric ulcer Aliases: acute gastric ulcer with haemorrhage and perforation acute gastric ulcer with hemorrhage AND with perforation but without obstruction acute gastric ulcer with hemorrhage and obstruction acute gastric ulcer with hemorrhage and perforation acute gastric ulcer with hemorrhage and perforation, with obstruction acute gastric ulcer with hemorrhage and perforation, without mention of obstruction acute gastric ulcer with hemorrhage, with obstruction acute gastric ulcer with hemorrhage, with perforation AND with obstruction acute gastric ulcer with perforation acute gastric ulcer with perforation AND obstruction acute gastric ulcer with perforation, with obstruction acute gastric ulcer without hemorrhage and without perforation acute gastric ulcer without hemorrhage, without perforation AND without obstruction acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction bleeding acute gastric ulcer chronic gastric ulcer without hemorrhage AND without perforation chronic gastric ulcer without hemorrhage AND without perforation but with obstruction chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction	ACE BAD CAT CYP2C19 CYP2C9 EFNA5 FUT4 GPX1 IDUA LGALS1 MGLL PLA2G4A PTGS1 PTGS2 TFF1	11343 1557 1559 1636 1946 2526 2876 3425 3956 5321 572 5742 5743 7031 847	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:9637	stomatitis	CAT CYP2B6 FCGR3B MICA PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PPT1 PSAP PTGS2 UGT1A1 UNG	100507436 142 1555 2215 5290 5291 5293 5294 54658 5538 5660 5743 7374 847	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9673	ulcerative stomatitis	CAT FCGR3B MICA PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PPT1 PSAP UGT1A1 UNG	100507436 142 2215 5290 5291 5293 5294 54658 5538 5660 7374 847	Homo sapiens (human)	DisGeNET DisGeNET

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