GlyCosmos Portal

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

Displaying entries **1501 - 1525** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0060731	congenital central hypoventilation syndrome Aliases: CCHS Ondine curse Ondine syndrome central congenital hypoventilation syndrome congenital central alveolar hypoventilation syndrome	Bdnf	12064	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1205	allergic disease Aliases: allergic hypersensitivity disease hypersensitivity hypersensitivity reaction type I disease	Ace Agt Akr1b1 Cd14 Cysltr1 Fcgr3a Icam1 Il13 Lta	114099 116553 24179 24192 24310 25008 25464 304966 60350	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112263	hypoinsulinemic hypoglycemia with hemihypertrophy Aliases: HIHGHH hypoinsulinemic hypoglycemia and body hemihypertrophy	Akt2	11652	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081138	agammaglobulinemia 6	CD79B	974	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110414	retinitis pigmentosa 3 Aliases: RP3	Rpgr	19893	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050859	hemorrhagic cystitis	GLR1	856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111301	generalized epilepsy with febrile seizures plus 9 Aliases: GEFS+9 GEFSP9 generalised epilepsy with febrile seizures plus 9 generalised epilepsy with febrile seizures plus type 9 generalized epilepsy with febrile seizures plus type 9	Stx1b	56216	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050625	biliary tract benign neoplasm Aliases: extrahepatic bile duct neoplasm neoplasm of extrahepatic bile ducts tumor of the extrahepatic bile duct	Faslg Hgf Il4	24446 25385 287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2977	primary hyperoxaluria	AGXT GRHPR HOGA1	112817 189 9380	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110123	Bardet-Biedl syndrome 1 Aliases: BBS1	Arl6	56297	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060036	intrinsic cardiomyopathy	CCT4	851412	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080608	anterior segment dysgenesis 3	FOXC1	2296	Homo sapiens (human)	Alliance of Genome Resources
DOID:5353	colonic disease Aliases: colon disorder	Ghr	25235	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11151	cholecystolithiasis	ATG26	850886	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12559	idiopathic juvenile osteoporosis Aliases: Idiopathic osteoporosis juvenile osteoporosis	Lrp5	16973	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1907	malignant fibrous histiocytoma Aliases: Fibroxanthosarcoma MFH	Ppargc1a	19017	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110605	primary ciliary dyskinesia 7 Aliases: CILD7 primary ciliary dyskinesia 7 with or without situs inversus	Dnah11	13411	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:104	bacterial infectious disease	OST3	854252	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110163	Charcot-Marie-Tooth disease axonal type 2F Aliases: CMT2F Charcot-Marie-Tooth neuronal type 2F Charcot-Marie-Tooth neuropathy type 2F autosomal dominant Charcot-Marie-Tooth disease type 2F	HSPB1	3315	Homo sapiens (human)	Alliance of Genome Resources
DOID:2988	antiphospholipid syndrome Aliases: APS antiphospholipid antibody syndrome	Apoh Cd40lg H2-Aa H2-Ab1 H2-Eb1 Pf4 Plat Proc	11818 14960 14961 14969 18791 19123 21947 56744	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12053	cryptococcosis Aliases: Busse-Buschke's disease European cryptococcosis cryptococcal infection torula torulosis	CHIA	27159	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070048	GAND syndrome Aliases: MRD18 autosomal dominant intellectual developmental disorder 18 autosomal dominant mental retardation 18 autosomal dominant non-syndromic intellectual disability 18	GATAD2B	57459	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090050	dystonia 27	COL6A3	1293	Homo sapiens (human)	Alliance of Genome Resources
DOID:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	Gck Hk1 Hk2 Hk3 Igf1r Insrr Irs1 Rps6kb1 Tlr4	24385 25058 25059 25060 25467 25718 29260 60663 83840	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060040	pervasive developmental disorder Aliases: Pervasive Child Development Disorders pervasive development disorder	drd5.S	108705891	Xenopus laevis (African clawed frog)	Alliance of Genome Resources

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