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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 **3251 - 3275** of **4649** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:11870	Pick's disease Aliases: Dementia in Pick's disease LOBAR ATROPHY OF BRAIN PICK DISEASE OF BRAIN Pick disease	ATF2 CREB1 FOS MAP2K6 MAPT SNCA SNCB TARDBP	1385 1386 23435 2353 4137 5608 6620 6622	Homo sapiens (human)	Alliance of Genome Resources
DOID:1188	mononeuropathy	GAL	51083	Homo sapiens (human)	Alliance of Genome Resources
DOID:1192	peripheral nervous system neoplasm Aliases: neoplasm of peripheral nerve nerve sheath neoplasm tumor of PNS	PTEN	5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:11934	head and neck cancer Aliases: head and neck neoplasm head and neck tumours head/neck neoplasm tumor of head and neck	CYP1A1 KDM4C	1543 23081	Homo sapiens (human)	Alliance of Genome Resources
DOID:11949	Creutzfeldt-Jakob disease Aliases: CJD Creutzfeldt Jacob syndrome Creutzfeldt Jakob disease Creutzfeldt-Jacob disease Jakob-Creutzfeldt disease Subacute spongiform encephalopathy Transmissible virus dementia	GALC HLA-DQB1 MAPT NEFH NEFL PRNP PTGS1 PTGS2 SERPINA3 SNCA STX1A YWHAG	12 2581 3119 4137 4744 4747 5621 5742 5743 6622 6804 7532	Homo sapiens (human)	Alliance of Genome Resources
DOID:11963	esophagitis Aliases: acute esophagitis	BMP4 IL4R PTGS2 SLC7A5 TNF	3566 5743 652 7124 8140	Homo sapiens (human)	Alliance of Genome Resources
DOID:11981	morbid obesity Aliases: Severe obesity	ACSS2 AGER CCK CPE CTNNBL1 CYP2E1 GHRL HIF1A IL1RN LPIN1 MC4R MCHR1 NPPB NPY2R NTRK2	1363 1571 177 23175 2847 3091 3557 4160 4879 4887 4915 51738 55902 56259 885	Homo sapiens (human)	Alliance of Genome Resources
DOID:11983	Prader-Willi syndrome Aliases: Prader Willi syndrome	GHRL HTR2C MAGEL2	3358 51738 54551	Homo sapiens (human)	Alliance of Genome Resources
DOID:11984	hypertrophic cardiomyopathy Aliases: hypertrophic obstructive cardiomyopathy	ACE2 ACE ACTB ADGRL4 ADM AGT AHR CACNB2 CD36 CMA1 CS CTSL CYP1A1 CYP1B1 CYP2E1 DNMT1 DSP EDN1 EPHX2 FHL1 HRAS HTR2B ICAM1 IGF1R KRAS LAMP2 MAP3K7 MMP1 MMP2 MMP9 MYBPC3 MYH7 NPPA NPPB NRAS ORAI1 ORAI3 PKD1 PTPN11 SDHD SLC25A6 STIM1 STIM2 TNNI3 VCL XIRP1	1215 133 1431 1514 1543 1545 1571 1636 165904 1786 183 1832 1906 196 2053 2273 293 3265 3357 3383 3480 3845 3920 4312 4313 4318 4607 4625 4878 4879 4893 5310 57620 5781 59272 60 6392 64123 6786 6885 7137 7414 783 84876 93129 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:11994	atrophy of testis	BRCA2	675	Homo sapiens (human)	Alliance of Genome Resources
DOID:11996	spermatic cord torsion Aliases: Torsion of testicle Torsion of testis testicular Torsion	GPX3	2878	Homo sapiens (human)	Alliance of Genome Resources
DOID:12010	anterior ischemic optic neuropathy Aliases: Ischemic optic neuropathy	CSF3 NOS3	1440 4846	Homo sapiens (human)	Alliance of Genome Resources
DOID:12029	sympathetic ophthalmia Aliases: Sympathetic uveitis	HLA-DRB1	3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:12030	panuveitis Aliases: Diffuse uveitis	CFH IFNG IL10	3075 3458 3586	Homo sapiens (human)	Alliance of Genome Resources
DOID:1205	allergic disease Aliases: allergic hypersensitivity disease hypersensitivity hypersensitivity reaction type I disease	ACE AGT AKR1B1 CD14 CYSLTR1 FCGR3A HLA-DQA1 HLA-DQB1 HLA-DRA HLA-DRB1 ICAM1 IL13 LTA MIF TAP1	10800 1636 183 2214 231 3117 3119 3122 3123 3383 3596 4049 4282 6890 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:12053	cryptococcosis Aliases: Busse-Buschke's disease European cryptococcosis cryptococcal infection torula torulosis	CHIA	27159	Homo sapiens (human)	Alliance of Genome Resources
DOID:1206	Rett syndrome Aliases: Rett's disorder cerebroatrophic hyperammonemia	ADIPOQ CDKL5 MECP2	4204 6792 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:12098	trigeminal neuralgia Aliases: Trifacial neuralgia trifocal neuralgia	CDK5 GABRG1	1020 2565	Homo sapiens (human)	Alliance of Genome Resources
DOID:1210	optic neuritis	AQP4 CAT CCR5 HLA-DQB1 HLA-DRB1 MOG NEFH SOD2	1234 3119 3123 361 4340 4744 6648 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:12117	pulmonary alveolar microlithiasis	SLC34A2	10568	Homo sapiens (human)	Alliance of Genome Resources
DOID:12119	hemosiderosis Aliases: haemosiderosis	CP	1356	Homo sapiens (human)	Alliance of Genome Resources
DOID:12120	pulmonary alveolar proteinosis	ABCA3 CSF2 CSF2RA CSF2RB DEFB1 MARS1 SFTPA1 SFTPB SFTPC SFTPD	1437 1438 1439 1672 21 4141 6439 6440 6441 653509	Homo sapiens (human)	Alliance of Genome Resources
DOID:12129	bulimia nervosa Aliases: hyperorexia nervosa	COMT	1312	Homo sapiens (human)	Alliance of Genome Resources
DOID:12132	granulomatosis with polyangiitis Aliases: Necrotizing respiratory granulomatosis Wegener granulomatosis, formerly	CCR3 CCR5 CD36 CD40LG CTLA4 FCAR IL10 THBD VTN	1232 1234 1493 2204 3586 7056 7448 948 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:12134	factor VIII deficiency Aliases: Congenital factor VIII disorder Hemophilia A Subhemophilia classic hemophilia A	C3 C5 CFB CFP F2 F8 FCGR2A HLA-DQA1 IFNG IL10 PLAT TFPI TGFB1	2147 2157 2212 3117 3458 3586 5199 5327 629 7035 7040 718 727	Homo sapiens (human)	Alliance of Genome Resources

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