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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 **4351 - 4375** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:11123	Henoch-Schoenlein purpura Aliases: Allergic purpura Autoimmune purpura Henoch-Sch?nlein purpura Henoch-Sch@nlein purpura Henoch-Scholein purpura Henoch-Schonlein Purpura Purpura, autoimmune	ACE AGT CCL2 CD86 HLA-DQA1 IL1RN IL5 KNG1 MEFV PLAT PON1	1636 183 3117 3557 3567 3827 4210 5327 5444 6347 942	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050152	aspiration pneumonia	ACE EDN1 IL1A TNF	1636 1906 3552 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:8432	polycythemia Aliases: Erythrocythemia	ACE EPAS1 EPOR HBB SERPINE1	1636 2034 2057 3043 5054	Homo sapiens (human)	Alliance of Genome Resources
DOID:2355	anemia Aliases: anaemia	ACE ANK1 APC BMP6 EPO EPOR G6PD GDF15 GPX1 HBB HK1 IL10 IREB2 PON1 SLC11A2 SLC4A10 SLC4A11 SLC4A1 SLC4A2 SLC4A4 SLC4A5 SLC4A7 SLC4A8 SLC4A9 TF TNF TNFRSF1A VCAM1	1636 2056 2057 2539 286 2876 3043 3098 324 3586 3658 4891 5444 57282 57835 6521 6522 654 7018 7124 7132 7412 83697 83959 8671 9497 9498 9518	Homo sapiens (human)	Alliance of Genome Resources
DOID:4481	allergic rhinitis Aliases: Non-seasonal allergic rhinitis Perenial allergic rhinitis atopic rhinitis hay fever pollenosis seasonal allergic rhinitis	ABCB1 ACE CCL11 CD40 CD40LG F2 FCGR3A HLA-G IFNG IL10 IL13 IL13RA2 IL17A IL2 IL4 IL5 ITGB2 MUC1 MUC5AC NOD2 PON1 PRKG1 TACR1 TGFB1 TLR2 TLR4 TLR9	1636 2147 2214 3135 3458 3558 3565 3567 3586 3596 3598 3605 3689 4582 4586 5243 54106 5444 5592 6356 64127 6869 7040 7097 7099 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050864	non-arteritic anterior ischemic optic neuropathy Aliases: non-arteritic anterior ischaemic optic neuropathy nonarteritic anterior ischaemic optic neuropathy nonarteritic anterior ischemic optic neuropathy	ACE F5 GP1BA ITGB3	1636 2153 2811 3690	Homo sapiens (human)	Alliance of Genome Resources
DOID:11400	pyelonephritis	ACE AMBP B2M BMP7 CALCA CFB CXCR1 IL1RN IL3 PGF TLR1	1636 259 3557 3562 3577 5228 567 629 655 7096 796	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060071	pre-malignant neoplasm	ACE ATM BAX CASP9 FAS GLI1 GLI3 INSR MAPK9 MUC2 PPM1D SFTPD SHH SMAD4 SMO STAT3 TP53	1636 2735 2737 355 3643 4089 4583 472 5601 581 6441 6469 6608 6774 7157 842 8493	Homo sapiens (human)	Alliance of Genome Resources
DOID:8970	subacute sclerosing panencephalitis Aliases: Immunosuppressive measles encephalitis Van Bogaert's sclerosing leukoencephalitis subacute sclerosing leukoencephalopathy	ACE IFNL1	1636 282618	Homo sapiens (human)	Alliance of Genome Resources
DOID:9775	diastolic heart failure	ACE LEPR	1636 3953	Homo sapiens (human)	Alliance of Genome Resources
DOID:3500	gallbladder adenocarcinoma Aliases: adenocarcinoma of the gallbladder	ACE DDR2	1636 4921	Homo sapiens (human)	Alliance of Genome Resources
DOID:12986	leukostasis	ACE SERPINF1	1636 5176	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111128	focal segmental glomerulosclerosis 1 Aliases: FSGS1	ACE ACTN1 ACTN2 ACTN4	1636 81 87 88	Homo sapiens (human)	Alliance of Genome Resources
DOID:61	mitral valve disease Aliases: Mitral RH valve dis. Rheumatic mitral insufficiency Rheumatic mitral valve changes Rheumatic mitral valve regurgitation chronic rheumatic mitral valve disease of mitral valve rheumatic disease of mitral valve rheumatic mitral valve incompetence	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:790	ocular hypotension Aliases: Hypotony of eye	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070279	primary autosomal recessive microcephaly 14 Aliases: MCPH14	SASS6	163786	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050632	oculocutaneous albinism	DCT OCA2 SLC45A2 TYR TYRP1	1638 4948 51151 7299 7306	Homo sapiens (human)	Alliance of Genome Resources
DOID:231	motor neuron disease	DCTN1 KIF5B NOS1 SOD1 TARDBP VAPA VAPB VWA1	1639 23435 3799 4842 64856 6647 9217 9218	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060193	amyotrophic lateral sclerosis type 1 Aliases: ALS1 amyotrophic lateral sclerosis 1	DCTN1 NEFH PRPH SNCG SOD1 SOD2 VEGFA	1639 4744 5630 6623 6647 6648 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111202	autosomal dominant distal hereditary motor neuronopathy 14 Aliases: DHMN7B HMN VIIB HMN7B Harper-Young myopathy distal hereditary motor neuronopathy type 7B distal hereditary motor neuropathy type VIIB distal spinal muscular atrophy with vocal cord paralysis type 7B	DCTN1	1639	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	DCTN1	1639	Homo sapiens (human)	Alliance of Genome Resources
DOID:2219	Glanzmann's thrombasthenia Aliases: BDPLT2 Glanzmann thrombasthenia Glycoprotein IIb/IIIa defect Thrombocytasthenia deficiency of GP IIb-IIIa complex deficiency of glycoprotein complex IIb-IIIa deficiency of platelet fibrinogen receptor platelet glycoprotein IIb-IIIa deficiency platelet-type bleeding disorder 2 thrombasthenia of Glanzmann and Naegeli	Itga2 Itga2b Itgb3	16398 16399 16416	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060573	von Willebrand's disease 1 Aliases: VWD type 1 VWD1 von Willebrand disease type 1 von Willebrand disease type I	Itga2 Itga2b Plat Vwf	16398 16399 18791 22371	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060691	platelet-type bleeding disorder 16 Aliases: autosomal dominant Glanzmann thrombasthenia autosomal dominant thrombasthenia of Glanzmann and Naegeli	Itga2b Itgb3	16399 16416	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060737	junctional epidermolysis bullosa Herlitz type Aliases: Herlitz type epidermolysis bullosa junctionalis Herlitz-Pearson-type epidermolysis bullosa JEB-H JEB-Herlitz type epidermolysis bullosa letalis junctional epidermolysis bullosa generalisata gravis junctional epidermolysis bullosa, Herlitz-Pearson type	Itga6 Lamb3 Lamc2	16403 16780 16782	Mus musculus (house mouse)	Alliance of Genome Resources

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