GlyCosmos Portal

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Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1076 - 1100** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:0070227	intrahepatic cholestasis of pregnancy Aliases: ICP gravidic intrahepatic cholestasis pregnancy related cholestasis recurrent intrahepatic cholestasis of pregnancy	ACE CHI3L1 HPRT1 ISYNA1 KLB PLA2G1B PLA2G2A PLA2G6 PNPLA3 PTGES3 SLC17A5 VCAM1	10728 1116 152831 1636 26503 3251 51477 5319 5320 7412 80339 8398	Homo sapiens (human)
DOID:7693	abdominal aortic aneurysm Aliases: AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1	ABO ACE ACLY ACSS2 ALOX5 APRT ARSA ARSI CAT CD14 CD1D CD22 CD44 CNTN3 CTSA CYP19A1 CYP2J2 DCN EFNA5 FCGR3B FCN3 HPSE ICAM1 ICAM2 IL18R1 IL1R1 LGALS3 LTA4H LTC4S MBD4 MCAT PARP1 PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G10 PLA2G15 PLA2G7 PRKAA2 PTEN PTGES PTGS2 RECK RENBP SELL SLC33A1 SMUG1 SRD5A1 TM7SF2 VCAM1 VCAN XYLT1	10855 142 1462 1573 1588 1634 1636 1946 2215 23583 23659 240 27349 28 3383 3384 340075 353 3554 3958 4048 4056 410 47 5067 5130 5290 5291 5293 5294 5476 5563 55902 5728 5743 5973 6402 64131 6715 7108 7412 7941 8399 8434 847 8547 8809 8930 912 9197 929 933 9536 960	Homo sapiens (human)
DOID:1123	spondyloarthropathy Aliases: spondarthropathy spondylarthrosis	ACAN ACE ALDOA CD14 CD74 CYP17A1 ENO1 ENPP1 FCGR3B KL KLRB1 KLRK1 MBL2 MICA PTGS2 SFTPA2 SMUG1 SOAT1 TNF VCAN	100507436 1462 1586 1636 176 2023 2215 226 22914 23583 3820 4153 5167 5743 6646 7124 729238 929 9365 972	Homo sapiens (human)
DOID:0050690	brachyolmia Aliases: brachyrachia	PAPSS2	9060	Homo sapiens (human)
DOID:0050954	spinocerebellar ataxia type 1	CAT ELOVL5 GLO1 HSD17B6	2739 60481 847 8630	Homo sapiens (human)
DOID:0110219	Brugada syndrome 2 Aliases: BRGDA2	Gpdh1	33824	Drosophila melanogaster (fruit fly)
DOID:0050152	aspiration pneumonia	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:0060322	mastoiditis	Tlr4	29260	Rattus norvegicus (Norway rat)
DOID:2994	germ cell cancer Aliases: malignant tumor of the germ cell	ACE AKR1C1 AKR1C3 ALPP AMACR ATRNL1 CALR CD44 CLEC10A CYP19A1 DHDH GFRA1 GOLPH3 GPC3 HPGDS IDH1 IDH2 LGALS3 LIPG LPL PARP1 PCYT1A PIGF PIK3CA PIK3CB PIK3CD PIK3CG PRSS21 PSMD10 PTEN SLC2A3 SMUG1 TDG TKTL1	10462 10942 142 1588 1636 1645 23583 23600 250 26033 2674 2719 27294 27306 3417 3418 3958 4023 5130 5281 5290 5291 5293 5294 5716 5728 64083 6515 6996 811 8277 8644 9388 960	Homo sapiens (human)
DOID:0050565	autosomal recessive nonsyndromic deafness	F38B6.6	185454	Caenorhabditis elegans
DOID:3151	skin squamous cell carcinoma Aliases: Epidermoid skin carcinoma	AKR1C3 APRT CD44 CD55 CDH13 CYP21A2 FUT1 GLB1 HPGDS HSD11B2 INPP5A MMUT NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGDS PTGS2 SDC1 SDC2 SIRT6 SMUG1 SOAT1 SPHK2 ST3GAL1 STT3A	1012 1589 1604 23583 2523 2720 27306 3291 353 3632 3703 4594 4684 51548 5290 5291 5293 5294 56848 5728 5730 5743 6382 6383 6482 6646 8644 960	Homo sapiens (human)
DOID:0070459	hereditary spastic paraplegia 90A Aliases: SPG90A autosomal dominant spastic paraplegia 90A	SPTSSA	171546	Homo sapiens (human)
DOID:0110516	autosomal recessive nonsyndromic deafness 65 Aliases: DFNB65 autosomal recessive deafness 65	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	L2HGDH	35156	Drosophila melanogaster (fruit fly)
DOID:0080411	familial adenomatous polyposis 3	NTG1 NTG2	851218 854114	Saccharomyces cerevisiae S288C
DOID:0050866	oral squamous cell carcinoma Aliases: mouth squamous cell carcinoma	Gapdh Gsk3b Tnf Tp53	24383 24835 24842 84027	Rattus norvegicus (Norway rat)
DOID:0112072	nuclear type mitochondrial complex I deficiency 20 Aliases: ACAD9 deficiency Acyl-CoA dehydrogenase 9 deficiency MC1DN20 mitochondrial complex 1 deficiency due to ACAD9 deficiency	ACADL	33	Homo sapiens (human)
DOID:0070077	schizophrenia 1 Aliases: SCZD1	SULT1E1	6783	Homo sapiens (human)
DOID:0110667	congenital myasthenic syndrome 5 Aliases: CMS Ic CMS5 EAD Engel congenital myasthenic syndrome congenital myasthenic syndrome Engel type congenital myasthenic syndrome type Ic end plate acetylcholinesterase deficiency	ACHE	43	Homo sapiens (human)
DOID:1883	hepatitis C Aliases: NANBH Viral hepatitis C chronic hepatitis C hepatitis C infection hepatitis nonA nonB	Myc	24577	Rattus norvegicus (Norway rat)
DOID:627	severe combined immunodeficiency Aliases: SCID combined T and B cell inborn immunodeficiency	AMACR CD38 CEACAM5 CEACAM7 CYP2J2 EXTL3 FUT1 GPC5 HPSE IL18R1 LDHC LGALS1 MELTF NCAM1 NT5E PARP1 PDHX PGM3 PIK3CA PIK3CB PIK3CD PIK3CG PNP PTEN PTGS2 SOAT1 SRGN	1048 10855 1087 142 1573 2137 2262 23600 2523 3948 3956 4241 4684 4860 4907 5238 5290 5291 5293 5294 5552 5728 5743 6646 8050 8809 952	Homo sapiens (human)
DOID:3275	thymoma	CAT CD44 CD74 CLEC14A G6PD GAPDH GPX1 HACD1 HSD17B7 ICAM1 LY75 MICA MSLN PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTEN PTGES2 PTGES PTGS2 SMUG1 SULT1E1	100507436 10232 142 161198 23583 2539 2597 2876 3383 4065 51478 5290 5291 5293 5294 5716 5728 5743 6783 80142 847 9200 9536 960 972	Homo sapiens (human)
DOID:4467	clear cell renal cell carcinoma Aliases: Clear cell carcinoma of kidney clear cell kidney carcinoma conventional (Clear cell) renal cell carcinoma conventional renal cell carcinoma renal clear cell carcinoma	Myc Tp53	24577 24842	Rattus norvegicus (Norway rat)
DOID:0080028	spondyloepimetaphyseal dysplasia, Strudwick type	PCYT1A	5130	Homo sapiens (human)
DOID:496	spindle cell hemangioma Aliases: SCH	ANXA5 IDH1 IDH2 PRKAA2 PTGS1 PTGS2	308 3417 3418 5563 5742 5743	Homo sapiens (human)

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