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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 **8551 - 8575** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:3179	inverted papilloma Aliases: Inverted papilloma, squamous cell	Hgf Kdr Vegfa	15234 16542 22339	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080745	polymyositis	Hgf Ifng Il4 Mmp9 Robo1 Slit2 Tnfrsf1a Tnfrsf1b	15234 15978 16189 17395 19876 20563 21937 21938	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8472	localized scleroderma Aliases: Morphea Scleroderma, circumscribed or localised Scleroderma, circumscribed or localized circumscribed scleroderma localised morphea localised morphoea localised scleroderma localized morphea	Hgf Icam1 Il13 Mmp1a Tgfb1	15234 15894 16163 21803 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8997	polycythemia vera Aliases: Osler-Vaquez syndrome Polycythaemia rubra vera Proliferative polycythaemia chronic erythremia	Hfe	29199	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4971	myelofibrosis Aliases: Agnogenic myeloid metaplasia Aleukemic myelosis Megakaryocytic myelosclerosis bone Marrow Fibrosis myelosclerosis primary myelofibrosis	Hfe Tgfb1 Tp53	24842 29199 59086	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	Hfe Tfr2 Tnf	24835 288562 29199	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080177	hepatic veno-occlusive disease Aliases: veno-occlusive disease	Hfe Mmp9	29199 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8437	intestinal obstruction	Hfe Il10 Ptgs2	25325 29199 29527	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9663	aphthous stomatitis Aliases: Aphtha Aphthous ulceration Canker sore Oral aphthae oral ulcer	Hfe Hspd1 Il10 Tgfb1	25325 29199 59086 63868	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:853	polymyalgia rheumatica	Hfe Mbl2 Pecam1	15216 17195 18613	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8437	intestinal obstruction	Hfe Il10 Ptgs2	15216 16153 19225	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9663	aphthous stomatitis Aliases: Aphtha Aphthous ulceration Canker sore Oral aphthae oral ulcer	Hfe Hspd1 Il10 Tgfb1	15216 15510 16153 21803	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	Hfe Hjv Tfr2 Tnf	15216 21926 50765 69585	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3323	Sandhoff disease Aliases: Sandhoff Jatzkewitz disease	Hexo1 Hexo2 fdl	250735 31808 38528	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3320	Tay-Sachs disease Aliases: GM2 gangliosidosis, type 1 hexosaminidase A deficiency	Hexo1 Hexo2 fdl	250735 31808 38528	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:12377	spinal muscular atrophy	Hexo1 Hexo2 fdl	250735 31808 38528	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3323	Sandhoff disease Aliases: Sandhoff Jatzkewitz disease	Hexb	294673	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3323	Sandhoff disease Aliases: Sandhoff Jatzkewitz disease	Hexb	15212	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3320	Tay-Sachs disease Aliases: GM2 gangliosidosis, type 1 hexosaminidase A deficiency	Hexa	300757	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3320	Tay-Sachs disease Aliases: GM2 gangliosidosis, type 1 hexosaminidase A deficiency	Hexa	15211	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	Hex-t2	43191	Drosophila melanogaster (fruit fly)	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	Hex-t2 Snmp2	38868 43191	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	Hex-t2 Pgi PyK Zw	32974 35886 42620 43191	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9952	acute lymphoblastic leukemia Aliases: ALL acute lymphoblastic leukaemia acute lymphocytic leukaemia precursor lymphoblastic lymphoma/leukemia	Hex-t2 Mdr49 Mdr65 N Nup214 Pgi trx	31293 35886 36428 38726 41737 43191 46091	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:11717	neonatal diabetes Aliases: diabetes mellitus syndrome in newborn infant neonatal diabetes mellitus	Hex-t1	117364	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources

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