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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 **1751 - 1775** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:3308	embryonal carcinoma Aliases: primary extragonadal embryonal carcinoma	fgf8b	65089	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0090086	hypogonadotropic hypogonadism 6 with or without anosmia	fgf8b	65089	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:1911	endodermal sinus tumor Aliases: Hepatoid yolk sac tumour Yolk Sac neoplasm Yolk sac tumour endodermal sinus tumour infantile embryonal carcinoma yolk sac tumor	fgf8b	65089	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:11198	DiGeorge syndrome Aliases: 22q11.2 deletion syndrome DiGeorge sequence DiGeorge's syndrome Pharyngeal pouch syndrome	fgf8b ndst1a ndst1b vegfaa	100329944 30682 570459 65089	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:6419	tetralogy of Fallot Aliases: Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle	fgf8b jag1a popdc1	140421 415107 65089	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:10892	hypospadias Aliases: familial hypospadias	fgf8b fgfr2	352940 65089	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0090082	hypogonadotropic hypogonadism 20 with or without anosmia	fgf17	407737	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:65	connective tissue disease Aliases: connective tissue disorder disorder of connective tissue	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111595	congenital contractural arachnodactyly Aliases: Beals syndrome Beals-Hecht syndrome CCA arachnodactyly, contractural Beals type contractures, multiple with arachnodactyly distal arthrogryposis type 9 ear anomalies-contractures-dysplasia of bone with kyphoscoliosis	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111561	stiff skin syndrome Aliases: SSKS	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060218	CREST syndrome	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111150	autosomal dominant isolated ectopia lentis 1 Aliases: ECTOL1	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111243	acromicric dysplasia Aliases: ACMICD acromicric skeletal dysplasia	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111726	geleophysic dysplasia 2 Aliases: GPHYSD2	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3492	mixed connective tissue disease Aliases: Connective tissue disease overlap syndrome mixed collagen vascular disease	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050475	Weill-Marchesani syndrome Aliases: GEMSS syndrome Marchesani-Weill Syndrome Mesodermal Dysmorphodystrophy, Congenital Spherophakia Brachymorphia Syndrome congenital mesodermal dystrophy	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050646	distal arthrogryposis Aliases: Arthrogryposis Multiplex Congenita	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4783	mesangial proliferative glomerulonephritis	fbn-1 pat-2	176076 176240	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3627	aortic aneurysm Aliases: ruptured aortic aneurysm	fbn-1 hda-4	176076 181723	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060249	scoliosis	fbn-1 gon-1	176076 177850	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10609	rickets Aliases: active rickets	famk-1	181616	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110066	amelogenesis imperfecta type 1G Aliases: AI1G AIGFS ERS amelogenesis imperfecta and gingival fibromatosis syndrome amelogenesis imperfecta hypoplastic with nephrocalcinosis amelogenesis imperfecta type IG enamel-renal syndrome enamel-renal-gingival syndrome	famk-1	181616	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2187	amelogenesis imperfecta	famk-1	181616	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050445	X-linked dominant hypophosphatemic rickets Aliases: Hypophosphatemia, Vitamin D-Resistant Rickets Vitamin D-Resistant Rickets, X-Linked X-linked hypophosphatemia hypophosphatemic rickets X-linked dominant	famk-1 nep-2	181616 188090	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112025	female-restricted syndromic X-linked intellectual disability 99 Aliases: MRXS99F X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability female-restricted syndromic X-linked mental retardation 99	faf	43749	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources

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