GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4451 - 4475** of **5716** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:2987	familial Mediterranean fever Aliases: FMF benign paroxysmal peritonitis	ABCB1 ACE CYP3A4 MEFV NOD2 POMC SERPINE1 TLR4	1576 1636 4210 5054 5243 5443 64127 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:5325	Roberts syndrome Aliases: LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE RBS Roberts-Sc Phocomelia Syndrome SC phocomelia syndrome	ESCO2	157570	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050855	renal fibrosis	CYP2J2 FCAR GFER MMP1	1573 2204 2671 4312	Homo sapiens (human)	Alliance of Genome Resources
DOID:12689	acoustic neuroma Aliases: Vestibular Neurilemmoma Vestibular schwannoma	CYP2E1 VEGFA	1571 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:14018	alcoholic liver cirrhosis Aliases: Alcoholic Cirrhosis Alcoholic cirrhosis of liver Laennec's cirrhosis Laennec's cirrhosis, alcoholic Portal cirrhosis	ALDH2 CYP2E1 GABRG2 LEP SERPINE1 SOD2 TG	1571 217 2566 3952 5054 6648 7038	Homo sapiens (human)	Alliance of Genome Resources
DOID:11832	visual epilepsy Aliases: epilepsy, visual	Grik5 Grm8 Hrh3 Nfe2l2 Npy5r Pdgfb Scn2b Spp1 Tnf Tnfrsf1a Tnfrsf1b Vdac1 Vdac2	156767 24407 24628 24835 25340 25349 25353 25625 60590 83529 83531 83619 85268	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080665	warfarin resistance	CYP2C9	1559	Homo sapiens (human)	Alliance of Genome Resources
DOID:4195	hyperglycemia	CCL11 CYP2C9 GPX1 HP IL6 PDX1 PON1 SOD1 TF	1559 2876 3240 3569 3651 5444 6356 6647 7018	Homo sapiens (human)	Alliance of Genome Resources
DOID:9993	hypoglycemia Aliases: Hypoglycaemia	AGTR2 AKT2 CYP2C9 GCK GLUD1 HNF4A PPP1R3A UCP3	1559 186 208 2645 2746 3172 5506 7352	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050809	mucopolysaccharidosis IX	Hyal1	15586	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1073	renal hypertension	CYP2C8 CYP2J2 HSPA8 NPPA	1558 1573 3312 4878	Homo sapiens (human)	Alliance of Genome Resources
DOID:4661	multiple chemical sensitivity Aliases: 20th century disease chemical AIDS environmental illness idiopathic environmental illness total allergy syndrome	CYP2C19	1557	Homo sapiens (human)	Alliance of Genome Resources
DOID:13922	eosinophilic esophagitis	CYP2C19 TGFB1	1557 7040	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050073	invasive aspergillosis	CYP2C19 MBL2 PTX3 TLR4	1557 4153 5806 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:750	peptic ulcer disease Aliases: acute peptic ulcer with hemorrhage acute peptic ulcer with hemorrhage and perforation acute peptic ulcer without hemorrhage and without perforation	CYP2C19 HLA-DRB1	1557 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis HbSS disease Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease homozygous sickle cell disease sickle cell anaemia	APOB BCL11A C3 CFB CYP2C19 GPX1 HBB HLA-DQB1 NOS3	1557 2876 3043 3119 338 4846 53335 629 718	Homo sapiens (human)	Alliance of Genome Resources
DOID:14067	Plasmodium falciparum malaria Aliases: Malaria fever, subtertian falciparum malaria malignant tertian fever	ABO CYP2C19 FCGR2A G6PD HLA-DQB1 HP MBL2	1557 2212 2539 28 3119 3240 4153	Homo sapiens (human)	Alliance of Genome Resources
DOID:5520	head and neck squamous cell carcinoma Aliases: carcinoma of the head and neck squamous cell carcinoma of the head and neck squamous cell carcinomas of head and neck	CYP2C19 CYP2C9 FANCB FGFR4 IL2 JUNB OGG1 PTPN13 STAT3 TNFRSF10A TNFRSF10B	1557 1559 2187 2264 3558 3726 4968 5783 6774 8795 8797	Homo sapiens (human)	Alliance of Genome Resources
DOID:9007	sudden infant death syndrome Aliases: Cot death Crib death SIDS Sudden death of nonspecific cause in infancy	Slc6a4	15567	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8689	anorexia nervosa	Htr4	15562	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11983	Prader-Willi syndrome Aliases: Prader Willi syndrome	Htr2c	15560	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11984	hypertrophic cardiomyopathy Aliases: hypertrophic obstructive cardiomyopathy	Htr2b Pkd1 Ptpn11	15559 18763 19247	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2030	anxiety disorder Aliases: anxiety anxiety state	Htr1a	15550	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12716	newborn respiratory distress syndrome Aliases: HMD - Hyaline membrane disease Neonatal respiratory Distress syndrome hyaline membrane disease pulmonary hyaline membrane disease pulmonary hypoperfusion syndrome of newborn respiratory distress syndrome of newborn	Ndst1 Vegfa	15531 22339	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13481	thanatophoric dysplasia	Hspg2	15530	Mus musculus (house mouse)	Alliance of Genome Resources

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