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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 **3651 - 3675** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:2491	sensory peripheral neuropathy Aliases: peripheral Sensory Neuropathy sensory neuropathy	BACE1	23621	Homo sapiens (human)	Alliance of Genome Resources
DOID:2508	Takayasu's arteritis Aliases: Aortic arch arteritis Idiopathic aortitis Takayasu arteritis Takayasu's disease aortic arch syndrome	AGER HLA-A HLA-B HLA-DRB1 IL2 MMP3 MMP9	177 3105 3106 3123 3558 4314 4318	Homo sapiens (human)	Alliance of Genome Resources
DOID:251	alcohol-induced mental disorder	DRD2 FOXO4	1813 4303	Homo sapiens (human)	Alliance of Genome Resources
DOID:2512	nevoid basal cell carcinoma syndrome Aliases: Gorlin syndrome NBCCS basal cell nevus syndrome	GLI1 PTCH1 SHH SMO	2735 5727 6469 6608	Homo sapiens (human)	Alliance of Genome Resources
DOID:2513	basal cell carcinoma Aliases: Basal cell cancer Basal cell carcinoma of skin Basal cell neoplasm Basal cell tumor Epithelioma basal cell Rodent ulcer malignant Basal cell neoplasm malignant basal cell tumor	BAP1 CRNKL1 CTCF CTLA4 OCA2 OGG1 PTCH1 PTCH2 RASA1 SHH SMO TP53 XRCC5 XRCC6	10664 1493 2547 4948 4968 51340 5727 5921 6469 6608 7157 7520 8314 8643	Homo sapiens (human)	Alliance of Genome Resources
DOID:2518	orchitis Aliases: Inflammation of testis Orchititis	CCL2 CCL5 CCR5 CD86 IL6R PECAM1	1234 3570 5175 6347 6352 942	Homo sapiens (human)	Alliance of Genome Resources
DOID:252	alcoholic psychosis Aliases: Alcoholic psychoses	HTR2A	3356	Homo sapiens (human)	Alliance of Genome Resources
DOID:2526	prostate adenocarcinoma	ADIPOQ AKT1 AKT2 AKT3 AR BIN1 CD9 CLU CREB3L4 GRB2 IGF1R IKBKB INSR JUN KDR MAP2K1 MYC NCOA2 PAM PDGFA PDGFRA PIK3CB PRKCQ RAF1 RELA STAT1	10000 10499 1191 148327 207 208 274 2885 3480 3551 3643 367 3725 3791 4609 5066 5154 5156 5291 5588 5604 5894 5970 6772 928 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:2527	nephrosis	ACE ANGPT1 ANGPT2 CAT CCL1 CCL7 CD36 CD59 CFH CX3CL1 CYP11A1 CYP27B1 EDN1 F2 GATA3 GPX1 HAVCR1 LAMB2 LRP2 NES NPPA NPPB PDPN PTPRU SREBF2 VIM	10076 10630 10763 1583 1594 1636 1906 2147 2625 26762 284 285 2876 3075 3913 4036 4878 4879 6346 6354 6376 6721 7431 847 948 966	Homo sapiens (human)	Alliance of Genome Resources
DOID:2531	hematologic cancer Aliases: Hematologic malignancy Hematologic neoplasm Hematological tumors blood cancer hematopoietic and lymphoid system tumor hematopoietic cancer hematopoietic neoplasm hematopoietic tumors malignant hematopoietic neoplasm	CUX1 JAK1 JAK3 PIAS1 PIAS2 SLC19A1 TP53 TYK2	1523 3716 3718 6573 7157 7297 8554 9063	Homo sapiens (human)	Alliance of Genome Resources
DOID:2537	inflammatory and toxic neuropathy	HTR2A	3356	Homo sapiens (human)	Alliance of Genome Resources
DOID:2548	reflex epilepsy Aliases: epilepsy, sensory-induced	ABAT TRPV1	18 7442	Homo sapiens (human)	Alliance of Genome Resources
DOID:255	hemangioma	MMP2 SLC2A1	4313 6513	Homo sapiens (human)	Alliance of Genome Resources
DOID:2559	opiate dependence Aliases: Opioid type dependence	ABCB1 AKT1 BDNF BMPER C9 COMT DRD2 GAL NAV3 NGF NPY1R OPRD1 OPRK1 OPRM1 VEGFA	1312 168667 1813 207 4803 4886 4985 4986 4988 51083 5243 627 735 7422 89795	Homo sapiens (human)	Alliance of Genome Resources
DOID:2560	morphine dependence	ADRA2A AGO2 BAX BDNF COMT CREB1 DRD2 FADD FOS FOSB GAD1 GRIA1 NCAM1 NGF NPSR1 NR3C2 POMC	1312 1385 150 1813 2353 2354 2571 27161 2890 387129 4306 4684 4803 5443 581 627 8772	Homo sapiens (human)	Alliance of Genome Resources
DOID:2562	suppurative periapical periodontitis Aliases: Apical abscess Dentoalveolar abscess Periapical abscess Suppurative apical periodontitis	ELANE	1991	Homo sapiens (human)	Alliance of Genome Resources
DOID:2566	corneal dystrophy	ELOVL4 KERA TACSTD2 TGFBI	11081 4070 6785 7045	Homo sapiens (human)	Alliance of Genome Resources
DOID:2569	retinal drusen	CFH	3075	Homo sapiens (human)	Alliance of Genome Resources
DOID:2580	rhizomelic chondrodysplasia punctata Aliases: Chondrodysplasia Punctata, Rhizomelic Form	AGPS	8540	Homo sapiens (human)	Alliance of Genome Resources
DOID:2581	chondrodysplasia punctata Aliases: Chondrodysplasia punctata congenita	ARSL EBP MSMO1	10682 415 6307	Homo sapiens (human)	Alliance of Genome Resources
DOID:2582	acatalasia Aliases: acatalasemia deficiency of catalase	CAT	847	Homo sapiens (human)	Alliance of Genome Resources
DOID:2583	agammaglobulinemia Aliases: IGHM hypogammaglobulinemia mu heavy chain deficiency	BTK LRRC8A	56262 695	Homo sapiens (human)	Alliance of Genome Resources
DOID:2590	familial nephrotic syndrome Aliases: Congenital nephrotic syndrome	DAAM2 LAMA5	23500 3911	Homo sapiens (human)	Alliance of Genome Resources
DOID:2596	larynx cancer	CXCR4 ERCC5 ERCC6 GPX1 NOD2 VEGFA	2073 2074 2876 64127 7422 7852	Homo sapiens (human)	Alliance of Genome Resources
DOID:26	pancreas disease	MSLN	10232	Homo sapiens (human)	Alliance of Genome Resources

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