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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

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

Displaying entries **626 - 650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:0060419	chromosome 3q29 microdeletion syndrome Aliases: 3q subtelomere deletion syndrome 3q29 microdeletion syndrome 3q29 recurrent deletion 3qter deletion	osta-1 osta-2 osta-3	173966 175140 182062	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110868	congenital stationary night blindness 1D Aliases: CSNB1D congenital stationary night blindness 1D autosomal recessive	ncx-4	172834	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111404	Jalili syndrome Aliases: Cone rod dystrophy-amelogenesis imperfecta syndrome cone-rod dystrophy and amelogenesis imperfecta	cnnm-1 cnnm-3	178499 180591	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9834	hyperopia Aliases: Far-sightedness farsightedness hypermetropia	myrf-1 myrf-2	174614 181229	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3007	breast ductal carcinoma Aliases: duct carcinoma	F47E1.2 zig-11	181145 189580	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5241	hemangioblastoma Aliases: Capillary Hemangioblastoma	glp-1 lin-12 spe-9	173042 176282 176286	Caenorhabditis elegans	Alliance of Genome Resources
DOID:479	angiokeratoma Aliases: Angiokeratoma of skin Cutaneous Angiokeratoma skin angiokeratoma	gana-1	179660	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2044	drug-induced hepatitis Aliases: Drug-induced chronic hepatitis	mrp-1 mrp-2 mrp-7	180289 180408 180409	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112250	Gaucher's disease type IIIC Aliases: GD3C Gaucher disease type 3C Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome Gaucher-like disease cardiovascular Gaucher disease	gba-3 gba-4	177314 178535	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111970	immunodeficiency 10 Aliases: CID due to STIM1 deficiency IMD10 STIM1 deficiency combined immunodeficiency due to STIM1 deficiency immune dysfunction with T-cell inactivation due to calcium entry defect 2	stim-1	175201	Caenorhabditis elegans	Alliance of Genome Resources
DOID:540	strabismus	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1686	glaucoma	W01F3.2 acn-1 srp-3 zmp-4	178672 179991 180351 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081335	Becker disease	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112202	developmental and epileptic encephalopathy	unc-47	176431	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2154	nephroblastoma Aliases: adult nephroblastoma	cri-2 daf-2 dbl-1 let-23 mom-5 pgp-1 pgp-3 ver-1 ver-3 ver-4	172856 174462 175182 175410 178215 179068 179197 181289 181326 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9351	diabetes mellitus Aliases: diabetes	C53D5.5 T03D8.6 W03G11.3 cpr-3 cpr-4 cpr-6 cri-2 daf-2 folt-1 gspd-1 ida-1 let-23 ogt-1 prmn-1 ptp-3 ver-4 zmp-3	171619 174462 174685 175410 175807 176000 178046 178748 179053 179197 179544 180033 180364 180931 181330 186632 189173	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12930	dilated cardiomyopathy Aliases: primary dilated cardiomyopathy	W01F3.2 apx-1 cle-1 cpl-1 cri-2 cts-1 eef-1A.1 eef-1A.2 gpx-3 gpx-5 let-23 mef-2 nep-11 nep-1 pkc-2 stim-1 zmp-3 zmp-4	172678 172732 173685 174462 174787 175201 175975 176437 178748 178759 179197 179991 180111 180351 181044 181166 181178 182513	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12297	Vogt-Koyanagi-Harada disease Aliases: Harada's disease Vogt-Koyanagi syndrome uveomeningoencephalitic syndrome	pat-3	175504	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111278	histiocytosis-lymphadenopathy plus syndrome Aliases: Faisalabad histiocytosis H syndrome HJCD PHID Rosai–Dorfman disease SHML cutaneous hyperpigmentation with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss familial Rosai-Dorfman disease histiocytosis and lymphadenopathy with or without cutaneous, cardiac, and/or endocrine features, joint contractures and/or deafness histiocytosis with joint contractures and sensorineural deafness pigmented hypertrichosis with insulin-dependent diabetes mellitus sinus histiocytosis and massive lymphadenopathy	ent-2	181648	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	drag-1	190602	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070093	schizophrenia 18 Aliases: Chromosome 7q36.3 Duplication Syndrome, 362-Kb SCZD18	glt-4	188744	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8440	ileus Aliases: Ileus of intestine	W01F3.2 ver-1 zmp-2 zmp-4	175182 175383 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8881	rosacea Aliases: Acne roscea Acne, erythematosa	W01F3.2 zmp-4	179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112312	male infertility due to globozoospermia Aliases: globozoospermia syndrome	enpl-1	178014	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111583	carboxypeptidase N deficiency Aliases: anaphylotoxin inactivator deficiency deficiency of carboxypeptidase B	cpd-2 egl-21	177940 181684	Caenorhabditis elegans	Alliance of Genome Resources

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