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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 **11326 - 11350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:0050448	white sponge nevus Aliases: hereditary mucosal leukokeratosis white sponge nevus of Cannon	KRT13	3860	Homo sapiens (human)	Alliance of Genome Resources
DOID:9505	cannabis abuse Aliases: marijuana abuse	Ace vn	38657 41625	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:399	tuberculosis	Mvl vn	38657 42490	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070082	schizophrenia 6 Aliases: SCZD6	vn	38657	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2468	psychotic disorder Aliases: mental or behavioural disorder	vn	38657	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080434	developmental and epileptic encephalopathy 61 Aliases: DEE61 early infantile epileptic encephalopathy 61	adam22.L	386621	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:3635	congenital myasthenic syndrome	chrne.L	386670	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110677	congenital myasthenic syndrome 4B Aliases: CMS4B congenital myasthenic syndrome 4B fast-channel	chrne.L	386670	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110679	congenital myasthenic syndrome 4C Aliases: CMS Id CMS1D CMS4C FIM1 congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency congenital myasthenic syndrome type Id familial infantile myasthenia 1	chrne.L	386670	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110678	congenital myasthenic syndrome 4A Aliases: CMS Ia1 CMS1A1 CMS4A congenital myasthenic syndrome 4A slow-channel congenital myasthenic syndrometype Ia1	chrne.L	386670	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:585	nephrolithiasis Aliases: Stone - kidney/ureter kidney stones	kdr kdrl pdgfra	386856 554230 796537	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:12215	oligohydramnios Aliases: Oligohydramnios - delivered antepartum oligohydramnios delivered oligohydramnios	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:8683	myeloid sarcoma Aliases: Chloroma Extramedullary Myeloid tumor Granulocytic sarcoma	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:999	hypereosinophilic syndrome Aliases: Eosinophilic leukocytosis eosinophilia	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:4297	scimitar syndrome Aliases: Halasz syndrome congenital venolobar syndrome hypogenetic lung syndrome mirror-image lung syndrome pulmonary venolobar syndrome total anomalous pulmonary venous return vena cava bronchovascular syndrome	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:5603	T-cell acute lymphoblastic leukemia Aliases: Precursor T Lymphoblastic Leukemia T Acute Lymphoblastic Leukemia T-cell acute lymphocytic leukaemia T-cell leukemia T-cell lymphoblastic leukemia/lymphoma acute T cell leukemia precursor T-lymphoblastic lymphoma/leukemia	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:4202	brain stem glioma Aliases: Brainstem Neuroglial tumor	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:8549	chronic ulcer of skin Aliases: Callous ulcer Indolent ulcer	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:8719	in situ carcinoma	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2696	Leydig cell tumor Aliases: Leydig cell neoplasm	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:3840	craniopharyngioma Aliases: neoplasm of Rathke's Pouch	pdgfra	386856	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080377	peroxisomal biogenesis disorder	RHOA RHOB RHOC	387 388 389	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050665	fetal alcohol syndrome	RHOA	387	Homo sapiens (human)	Alliance of Genome Resources
DOID:2121	ectodermal dysplasia Aliases: Congenital ectodermal defect Congenital ectodermal dysplasia	KRT17 NECTIN1 WNT10A	3872 5818 80326	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050449	pachyonychia congenita Aliases: Jackson-Lawler Type Pachyonychia Congenita Jadassohn-Lewandowsky Syndrome PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE Pachyonychia Congenita Type 1	KRT17	3872	Homo sapiens (human)	Alliance of Genome Resources

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