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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 **15276 - 15300** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:178	vascular disease Aliases: vascular tissue disease	cri-2	179197	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11044	gastroschisis	daf-2 ver-1	175182 175410	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:11335	sarcoidosis Aliases: Boeck sarcoid lymphogranulomatosis	acn-1 smf-1 smf-2 smf-3	177044 180780 180939 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9562	primary ciliary dyskinesia Aliases: ciliary motility disorder immotile ciliary syndrome	kpc-1	173051	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090125	brain small vessel disease 1 Aliases: BSVD1 COL4A1-related brain small vessel disease with hemorrhage COL4A1-related familial vascular leukoencephalopathy COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy brain small vessel disease with Axenfeld-Riegar anomaly brain small vessel disease with hemorrhage brain small vessel disease with or without ocular anomalies infantile hemiparesis leukoencephalopathy with Axenfeld-Riegar anomaly	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
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:12140	Chagas disease Aliases: Chagas' disease chagas' disease with digestive system involvement chagas' disease with nervous system involvement chagas' disease with other organ involvement	gar-3	179962	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3908	lung non-small cell carcinoma Aliases: NSCLC Non-small cell lung cancer non-small cell lung carcinoma	T13H5.8 W01C8.5 W01F3.2 acr-15 acr-16 acr-2 acr-3 acr-7 adm-2 cdh-4 cht-1 cri-2 daf-1 ddr-2 dep-1 dpf-2 eat-2 gpx-3 gpx-5 hpo-15 hst-3.2 lad-2 lam-1 lam-2 let-23 lev-1 mrp-1 mrp-2 mrp-7 pat-3 pgp-1 pgp-3 pkc-2 sma-6 stim-1 ugt-61 unc-38 unc-63 ver-1 ver-4 zmp-4	172105 172150 174044 174262 174362 174437 174462 175072 175182 175201 175504 175590 176829 177078 177292 178215 178269 178934 179197 179235 179991 180289 180351 180408 180409 180622 180628 180836 180936 180937 180980 181166 181178 181326 181489 181579 182513 185500 186632 191602 3564879	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13533	osteopetrosis Aliases: Albers-Schonberg disease marble bone	abts-4	180943	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1064	cystinosis Aliases: cystine storage disease	ctns-1	174308	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111576	dehydrated hereditary stomatocytosis 1 Aliases: PSHK1 dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema pseudohyperkalemia edinburgh pseudohyperkalemia familial 1, due to red cell leak	pezo-1	182492	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3490	Noonan syndrome Aliases: Turner's phenotype, karyotype normal	srp-3	178672	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10211	cholelithiasis	ugt-61	185500	Caenorhabditis elegans	Alliance of Genome Resources
DOID:7004	ACTH-secreting pituitary adenoma Aliases: ACTH-Producing Pituitary Adenoma Corticotroph adenoma Corticotropinoma	ntr-1 ntr-2	184471 188227	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060695	hyperekplexia Aliases: Kok disease congenital stiff man syndrome familial startle disease hereditary hyperekplexia startle disease	glc-1 glc-2	172103 180086	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080390	nephrotic syndrome type 1 Aliases: Finnish congenital nephrosis	syg-2	181561	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4202	brain stem glioma Aliases: Brainstem Neuroglial tumor	ver-1	175182	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1115	sarcoma Aliases: connective and soft tissue neoplasm tumor of soft tissue and skeleton	dep-1 ver-1 ver-4	174437 175182 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060050	autoimmune disease of blood	C38H2.2	176455	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050902	medulloblastoma Aliases: CNS PNET CPNET Medulloblastoma, histologically defined brain medulloblastoma infratentorial primitive neuroectodermal tumor localized primitive neuroectodermal tumor	ptc-1 ptc-3 ver-1	173631 174274 175182	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2152	ovary epithelial cancer Aliases: Ovarian Surface epithelial-Stromal tumor	ost-1	176931	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2590	familial nephrotic syndrome Aliases: Congenital nephrotic syndrome	epi-1	177956	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8398	osteoarthritis Aliases: Osteoarthrosis and allied disorder degenerative arthritis degenerative joint disease hypertrophic arthritis osteoarthrosis	C27A7.3 W01F3.2 adm-2 daf-1 daf-2 dbl-1 ddr-2 enpp-1 grd-2 mua-3 mup-4 scav-2 scav-3 sma-6 srp-6 srp-7 ver-1 ver-3 ver-4 zmp-3 zmp-4	174044 175182 175410 176060 176430 176673 176787 176829 178748 179068 179125 179195 179663 179665 179991 180349 180351 180622 181289 181489 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110014	age related macular degeneration 1 Aliases: ARMD1 age related maculopathy 1	gldi-2 him-4	174116 181187	Caenorhabditis elegans	Alliance of Genome Resources

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