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 **6276 - 6300** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:12215	oligohydramnios Aliases: Oligohydramnios - delivered antepartum oligohydramnios delivered oligohydramnios	ACE ALG8 COG5 DHCR7 GCDH GMPPB PGAP2 PGAP3 PIGL PIGO PIGV PIGW PIGY POMT1 TALDO1	10466 10585 1636 1717 2639 27315 284098 29925 55650 6888 79053 84720 84992 93210 9487	Homo sapiens (human)
DOID:4079	heart valve disease Aliases: Valvular heart disease	Galnt1 Tnf	24835 79214	Rattus norvegicus (Norway rat)
DOID:784	chronic kidney disease Aliases: CKD CRF chronic kidney failure chronic renal disease chronic renal failure syndrome renal failure - chronic	DGA1	854419	Saccharomyces cerevisiae S288C
DOID:0014667	disease of metabolism Aliases: metabolic disease	pfk-1.1 pfk-1.2	179335 180583	Caenorhabditis elegans
DOID:0060611	abdominal obesity-metabolic syndrome	Lep Ppargc1a	25608 83516	Rattus norvegicus (Norway rat)
DOID:3146	lipid metabolism disorder Aliases: dyslipidemia fatty acid metabolism disorder	CPT2	38355	Drosophila melanogaster (fruit fly)
DOID:2156	ovarian germ cell cancer Aliases: germ cell neoplasm of Ovary germ cell tumor of ovary	PTEN	5728	Homo sapiens (human)
DOID:1056	oculocerebrorenal syndrome Aliases: Lowe syndrome lowe oculocerebrorenal syndrome oculocerebrorenal syndrome of Lowe	ARSH G6PD HPRT1 INPP5A INPP5D INPP5E INPP5K MTM1 NAGLU OCRL PAFAH1B1 PTEN	2539 3251 347527 3632 3635 4534 4669 4952 5048 51763 56623 5728	Homo sapiens (human)
DOID:0110286	obsolete autosomal recessive limb-girdle muscular dystrophy type 2R	ACAN ACE ACHE AGK AGL ALDH7A1 ALOX12 ALPP APRT ATRNL1 B3GALNT2 B4GALNT2 B4GAT1 CD44 CHKA CHKB CRPPA CTNS DAG1 DCN DPEP1 DPM1 DPM2 DPM3 ENO1 FKRP FKTN GAA GK GLB1 GMPPB GNE HACD1 HPGDS HSPG2 IDH2 IMPA1 INPP5B INPP5K LARGE1 LARGE2 LGALS3 MBL2 MGAM PARP1 PIK3C2A PMM2 POGLUT1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PRG2 PRKAA2 PYGM RGN RXYLT1 SDC2 SI SIRT2 SLC3A1 ST3GAL4 SYNJ1 SYNJ2	10020 10329 10585 11041 1119 1120 120071 124872 142 148789 1497 1605 1634 1636 176 178 1800 2023 2218 22933 239 250 2548 26033 2710 2720 27306 29925 29954 3339 3418 353 3612 3633 3958 4153 43 501 51763 5286 5373 54344 5553 55624 5563 55750 56983 5837 6383 6476 6484 6519 729920 79147 84197 84892 8813 8818 8867 8871 8972 9104 9200 9215 960	Homo sapiens (human)
DOID:5693	adult liposarcoma	CPM FASN GPNMB PIK3CA PIK3CB PIK3CD PIK3CG PNPLA2 PNPLA3 PTEN SDC1 SMUG1 STS	10457 1368 2194 23583 412 5290 5291 5293 5294 57104 5728 6382 80339	Homo sapiens (human)
DOID:13096	Sneddon syndrome Aliases: Idiopathic livedo reticularis with systemic involvement	ARSA	410	Homo sapiens (human)
DOID:11656	cicatricial pemphigoid Aliases: Cicatricial pemphigoid with ocular involvement Ocular pemphigoid benign mucous membrane pemphigoid benign mucous membrane pemphigoid with ocular involvement ocular pemphigus	AKR1C3 TNF	7124 8644	Homo sapiens (human)
DOID:9744	type 1 diabetes mellitus Aliases: IDDM insulin-dependent diabetes mellitus type I diabetes mellitus	ugt1a1 ugt1a6 xylt1	100135191 100145490 100489505	Xenopus tropicalis (tropical clawed frog)
DOID:12961	Poland syndrome Aliases: Poland's syndactyly	CS CYP51A1 MTM1 PIK3CA	1431 1595 4534 5290	Homo sapiens (human)
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	MGAT2	4247	Homo sapiens (human)
DOID:0080154	short chain acyl-CoA dehydrogenase deficiency	ACADS ACADSB DLD	1738 35 36	Homo sapiens (human)
DOID:0050642	hypochromic microcytic anemia	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:0060299	complement component 6 deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:4989	pancreatitis	Htr2a Lepr Tlr4	24536 29260 29595	Rattus norvegicus (Norway rat)
DOID:6271	gastric cardia adenocarcinoma Aliases: adenocarcinoma of Cardia of stomach	AKR1A1 OGG1 PLCE1 PTGS2 SHMT1 SI	10327 4968 51196 5743 6470 6476	Homo sapiens (human)
DOID:0090058	torsion dystonia with onset in infancy	ALDH5A1	7915	Homo sapiens (human)
DOID:0050816	urofacial syndrome Aliases: Ochoa syndrome hydronephrosis with peculiar facial expression	HPSE2 HPSE	10855 60495	Homo sapiens (human)
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	pomt2	100490100	Xenopus tropicalis (tropical clawed frog)
DOID:8929	atrophic gastritis Aliases: gastric atrophy	ABO ACACA ALDH2 CD44 CEACAM5 CHGA CYP2C19 CYP2E1 CYP3A4 DCN GAD1 GLUL GPI L1CAM NAGLU NGLY1 OGG1 PIK3CA PIK3CB PIK3CD PIK3CG PLCE1 PTEN PTGS2 TM7SF2 VTCN1	1048 1113 1557 1571 1576 1634 217 2571 2752 28 2821 31 3897 4669 4968 51196 5290 5291 5293 5294 55768 5728 5743 7108 79679 960	Homo sapiens (human)
DOID:12336	male infertility	ACE ACSBG2 ACSL6 ALDH2 ANXA5 ATP6V0A2 CAT CCDC115 CLC CLEC7A COMT CTNS CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP2B6 ENO1 ENO4 GALNTL5 GBA2 GPX3 HPGDS LDHC MPG OGG1 PDHA2 PDIA3 PGAM4 PIK3CA PIK3CB PIK3CD PIK3CG PPT1 RGN SRGN	1178 1312 1497 1543 1545 1555 1586 1588 1636 168391 2023 217 23305 23545 27306 2878 2923 308 387712 3948 4350 441531 4968 5161 5290 5291 5293 5294 5538 5552 57704 64581 81616 84317 847 9104	Homo sapiens (human)

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