GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **12626 - 12650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:12205	dengue disease Aliases: Dengue Fever breakbone fever classic dengue	CD209 F2 FCGR2A GC IFNL1	2147 2212 2638 282618 30835	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050598	extrapulmonary tuberculosis	CD209 CLEC4M EREG	10332 2069 30835	Homo sapiens (human)	Alliance of Genome Resources
DOID:1394	urinary schistosomiasis Aliases: Schistosoma Hematobium Infection Schistosoma haematobium Schistosoma hematobium infectious disease Schistosomiasis due to schistosoma haematobium Schistosomiasis of bladder Vesical schistosomiasis bladder Schistosomiasis cystitis with bilharziasis	CD1D CTLA4 IL5 STAT6	1493 3567 6778 912	Homo sapiens (human)	Alliance of Genome Resources
DOID:12206	dengue hemorrhagic fever Aliases: DHF	CD1D CD209 FCGR2A IFNL1 IL21 KIR3DS1 SLC6A4	2212 282618 30835 3813 59067 6532 912	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081146	common variable immunodeficiency 3	CD19	930	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110587	autosomal dominant nonsyndromic deafness 66 Aliases: DFNA66 autosomal dominant deafness 66	CD164	8763	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050120	hemophagocytic lymphohistiocytosis Aliases: haemophagocytic syndrome	CD163	9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:8476	Whipple disease Aliases: Whipple's disease intestinal lipodystrophy	CD163	9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:2280	hidradenitis suppurativa Aliases: Acne inversa, familial	CD163 LCN2 NCSTN TNF	23385 3934 7124 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:4325	Ebola hemorrhagic fever Aliases: Ebola virus disease	CD163 IL3	3562 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:11077	brucellosis Aliases: Maltese fever undulant fever	CD163 IFNG	3458 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:936	brain disease Aliases: encephalopathy	CD163 CPT2 DBR1 ENO2 MFF MYCBP2 NUP214 PTEN RANBP2 SLC6A4 STIM2 TJP1 UNC93B1	1376 2026 23077 51163 56947 5728 57620 5903 6532 7082 8021 81622 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:13254	diverticulitis of colon Aliases: colonic diverticular disease	CD163 CD68	9332 968	Homo sapiens (human)	Alliance of Genome Resources
DOID:2938	Epstein-Barr virus infectious disease Aliases: EBV Infection Epstein-Barr virus infection	CD163 CD68 FGFR2 HLA-DPB1 ITGB2 PTEN	2263 3115 3689 5728 9332 968	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050523	adult T-cell leukemia/lymphoma Aliases: Adult T-cell leukemia/lymphoma (HTLV-1 positive) adult T-cell leukemia	CD163 CD274 CD68 CD80 CD86 FAS IL10 IL5 IL6 JAK3 NOTCH1	29126 355 3567 3569 3586 3718 4851 9332 941 942 968	Homo sapiens (human)	Alliance of Genome Resources
DOID:4644	epidermolysis bullosa simplex	CD151 DST KRT5 MMP9 PLEC	3852 4318 5339 667 977	Homo sapiens (human)	Alliance of Genome Resources
DOID:10608	celiac disease Aliases: celiac sprue coeliac disease idiopathic steatorrhea	CD14 CTLA4 F2 HLA-DQA1 HLA-DQB1 HLA-DRB1 ICOS IFNG IL10 IL21 IL23R IL6 PON1 PON3	149233 1493 2147 29851 3117 3119 3123 3458 3569 3586 5444 5446 59067 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:8677	perinatal necrotizing enterocolitis Aliases: ENTEROCOLITIS NECROTIZING Necrotizing enterocolitis in fetus OR newborn Perinatal necrotising enterocolitis Pseudomembranous enterocolitis in newborn necrotizing enterocolitis	CD14 CD40 CD40LG EGF HBEGF IL10 IL10RB IL6 MUC2 PARP1 PLAUR PTAFR TJP1 TLR1 TLR2 TLR3 TLR4 TLR5 TLR6 TLR7 TLR9 TNF	10333 142 1839 1950 3569 3586 3588 4583 51284 5329 54106 5724 7082 7096 7097 7098 7099 7100 7124 929 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060036	intrinsic cardiomyopathy	CCT4	851412	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050548	hereditary sensory neuropathy Aliases: familial dysautonomia, type II hereditary sensory and autonomic neuropathy	CCT4	851412	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050548	hereditary sensory neuropathy Aliases: familial dysautonomia, type II hereditary sensory and autonomic neuropathy	CCT4 DNMT1 DST NTRK1 SCN11A SPTLC1 WNK1	10558 10575 11280 1786 4914 65125 667	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060036	intrinsic cardiomyopathy	CCT3 CCT4 CCT6A DAAM1 DSG2 MRPS33 MYH7 NPPA RPL27A RPS3	10575 1829 23002 4625 4878 51650 6157 6188 7203 908	Homo sapiens (human)	Alliance of Genome Resources
DOID:14791	Leber congenital amaurosis Aliases: LCA Leber's amaurosis Leber's congenital amaurosis Leber's disease	CCT2 CRB1 GUCY2D MYO7A PALS1 PRPH2 RDH11 RDH14	10576 23418 3000 4647 51109 57665 5961 64398	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050486	exanthem	CCR6	1235	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma Aliases: cutaneous T cell lymphoma cutaneous T-cell lymphoma	CCR6 IL4	1235 3565	Homo sapiens (human)	Alliance of Genome Resources

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