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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 **10176 - 10200** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:10024	migraine with aura Aliases: classic migraine	dop-2 tbh-1	179347 181639	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11721	glycogen storage disease VII Aliases: Glycogen storage disease 7 Glycogen storage disease, type VII Muscle phosphofructokinase deficiency glycogen storage disease type VII phosphofructokinase myopathy	pfk-1.1 pfk-1.2	179335 180583	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0014667	disease of metabolism Aliases: metabolic disease	pfk-1.1 pfk-1.2	179335 180583	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070069	autosomal dominant intellectual developmental disorder 39 Aliases: MRD39 autosomal dominant mental retardation 39 autosomal dominant non-syndromic intellectual disability 39	Myt1l	17933	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1068	juvenile glaucoma Aliases: Glaucoma of childhood	Myoc	17926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110727	neuronal ceroid lipofuscinosis 13 Aliases: CLN13 neuronal ceroid lipofuscinosis 13 Kufs type	tag-196	179240	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080558	congenital disorder of glycosylation If Aliases: congenital disorder of glycosylation 1f	mpdu-1	179218	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110495	autosomal recessive nonsyndromic deafness 37 Aliases: DFNB37 autosomal recessive deafness 37	Myo6	17920	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110552	autosomal dominant nonsyndromic deafness 22 Aliases: DFNA22 autosomal dominant deafness 22	Myo6	17920	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090114	Sorsby's fundus dystrophy Aliases: SFD hemorrhagic macular dystrophy pseudoinflammatory fundus dystrophy of Sorsby	cri-2	179197	Caenorhabditis elegans	Alliance of Genome Resources
DOID:178	vascular disease Aliases: vascular tissue disease	cri-2	179197	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14250	Down syndrome Aliases: Complete trisomy 21 syndrome Down's syndrome Down's syndrome - trisomy 21 Downs syndrome G Trisomy trisomy 21 syndrome	W01F3.2 cri-2 pad-2 zmp-4	179197 179991 180351 259529	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13099	Moyamoya disease Aliases: progressive intracranial arterial occlusion	cri-2 timp-1	179197 179199	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2006	preretinal fibrosis Aliases: Macular puckering of retina Macular retinal puckering cellophane maculopathy	cri-2 timp-1	179197 179199	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3744	cervical squamous cell carcinoma Aliases: squamous cell carcinoma of cervix squamous cell carcinoma of the Cervix Uteri	cri-2 timp-1 ver-4	179197 179199 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080559	congenital disorder of glycosylation Ig Aliases: ALG12-congenital disorder of glycosylation congenital disorder of glycosylation 1g	algn-12	179185	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060832	Griscelli syndrome type 1 Aliases: GS1 Griscelli syndrome with neurological impairment Griscelli syndrome, cutaneous and neurological type Griscelli-Prunieras syndrome type 1 hypopigmentation-neurologic impairment syndrome	Myo5a	17918	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110536	autosomal recessive nonsyndromic deafness 91 Aliases: DFNB91 autosomal recessive deafness 91	srp-6 srp-7	179125 179195	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13141	uveitis	acn-1 srp-6 srp-7	179125 179195 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080288	spinocerebellar ataxia 46	F09G2.8	179105	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111805	syndromic microphthalmia 6 Aliases: Bakrania-Ragge syndrome MCOPS6 anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia microphthalmia and pituitary anomalies microphthalmia with brain and digit anomalies syndromic microphthalmia type 6	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11963	esophagitis Aliases: acute esophagitis	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12185	otosclerosis	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:668	myositis ossificans Aliases: Myisitis ossificans Ossification - muscle	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1882	atrial heart septal defect Aliases: atrial septal defect atrioseptal defect auricular septal defect congenital atrial septal defect interatrial septal defect interauricular septal defect	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources

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