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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 **7576 - 7600** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:8564	lip cancer Aliases: malignant neoplasm of commissure of lip malignant neoplasm of external Lip, not specified as upper or lower malignant neoplasm of labial commissure of lip malignant neoplasm of lip malignant neoplasm of lip, external malignant neoplasm of lip, inner aspect malignant neoplasm of lip, vermilion border malignant neoplasm of lower lip, buccal aspect malignant neoplasm of lower lip, inner aspect malignant neoplasm of lower lip, mucosa malignant neoplasm of lower lip, oral aspect malignant neoplasm of oral aspect of lip, not specified whether upper or lower malignant neoplasm of other sites of lip malignant neoplasm of vermilion border of lip malignant tumor of commissure of lip malignant tumor of labial mucosa malignant tumor of lip malignant tumor of lower labial mucosa malignant tumor of the Lip malignant tumour of labial commissure malignant tumour of lip	IL10	3586	Homo sapiens (human)	Alliance of Genome Resources
DOID:118	pericardial effusion	IL10	3586	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110899	inflammatory bowel disease 28 Aliases: IBD28 early onset autosomal recessive inflammatory bowel disease 28	IL10RA	3587	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110909	inflammatory bowel disease 25 Aliases: IBD25 early onset autosomal recessive inflammatory bowel disease 25	IL10RB	3588	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060859	salmonellosis Aliases: Salmonella infection	IL12B	3593	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111950	immunodeficiency 29 Aliases: IL12B deficiency IMD29 MSMD due to complete IL12B deficiency MSMD due to complete interleukin 12B deficiency Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency immunodeficiency 29, mycobacteriosis	IL12B	3593	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111990	immunodeficiency 30 Aliases: IMD30 MSMD due to complete IL12RB1 deficiency MSMD due to complete interleukin 12 receptor beta 1 deficiency Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency	IL12RB1	3594	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:350	mastocytosis Aliases: mast cell hyperplasia	IL13 IL5RA KIT	3568 3596 3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:4376	milk allergy Aliases: milk allergic reaction	IL13	3596	Homo sapiens (human)	Alliance of Genome Resources
DOID:3326	purpura Aliases: Purpuric disorder	IL13	3596	Homo sapiens (human)	Alliance of Genome Resources
DOID:4378	peanut allergy Aliases: allergy to peanuts peanut allergic reaction	IL13	3596	Homo sapiens (human)	Alliance of Genome Resources
DOID:11573	listeriosis Aliases: Infection by Listeria monocytogenes Listeria infection	IL15 IL1RN	3557 3600	Homo sapiens (human)	Alliance of Genome Resources
DOID:11162	respiratory failure Aliases: acute and chronic respiratory failure acute respiratory Failure acute-on-chronic respiratory failure chronic respiratory failure respiratory insufficiency/failure	IL15 MBL2 NUP188 SFTPB	23511 3600 4153 6439	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060189	ileitis Aliases: Crohn's ileitis	IL17A SERPINA1 TLR2 TLR4	3605 5265 7097 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111996	immunodeficiency 51 Aliases: CANDF5 IMD51 familial candidiasis 5	IL17RA	23765	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090076	hypogonadotropic hypogonadism 18 with or without anosmia	IL17RD	54756	Homo sapiens (human)	Alliance of Genome Resources
DOID:4371	Schnitzler syndrome	IL1A IL1RN	3552 3557	Homo sapiens (human)	Alliance of Genome Resources
DOID:11030	corneal edema Aliases: Corneal oedema	IL1A	3552	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060645	chronic recurrent multifocal osteomyelitis Aliases: CRMO chronic multifocal osteomyelitis	IL1R1 IL1RN LPIN2 PSTPIP2	3554 3557 9050 9663	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050686	organ system cancer	IL1R2	7850	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112022	non-syndromic X-linked intellectual disability 21 Aliases: MRX21 MRX34 X-linked mental retardation 21 X-linked mental retardation 21/34 X-linked mental retardation 34	IL1RAPL1	11141	Homo sapiens (human)	Alliance of Genome Resources
DOID:9938	dacryocystitis	IL1RN	3557	Homo sapiens (human)	Alliance of Genome Resources
DOID:8927	learning disability Aliases: Academic skill disorder learning disorder	IL1RN	3557	Homo sapiens (human)	Alliance of Genome Resources
DOID:1532	pleural disease Aliases: disorder of pleura non-neoplastic pleural disease	IL1RN	3557	Homo sapiens (human)	Alliance of Genome Resources

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