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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 **9876 - 9900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:8670	eating disorder	hda-4	181723	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13603	obstructive jaundice Aliases: Cholestatic Jaundice Cholestatic jaundice syndrome Obstructive hyperbilirubinemia	C06G1.1 cfh-1	181720 185381	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110034	X-linked Alport syndrome Aliases: nephropathy and deafness, X-linked	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060263	porencephaly	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110033	autosomal recessive Alport syndrome	let-2	181708	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:0111547	retinal arterial tortuosity Aliases: RATOR retinal arteriolar tortuosity retinal hemorrhage with vascular tortuosity tortuosity of retinal arteries	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111740	X-linked deafness 6 Aliases: DFNX6	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:854	collagen disease Aliases: collagen disorder	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13223	uterine fibroid Aliases: Plexiform leiomyoma UTERUS FIBROMA leiomyoma of Corpus Uteri uterine leiomyoma	R193.2 let-2	181708 182256	Caenorhabditis elegans	Alliance of Genome Resources
DOID:6088	acute stress disorder Aliases: traumatic stress disorder	ace-1	181706	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:6652	diffuse idiopathic skeletal hyperostosis Aliases: Ankylosing vertebral hyperostosis DISH Disseminated idiopathic skeletal hyperostosis	ent-2	181648	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081141	agammaglobulinemia 9	zipt-7.2	181640	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10609	rickets Aliases: active rickets	famk-1	181616	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2187	amelogenesis imperfecta	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: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:0112209	developmental and epileptic encephalopathy 73 Aliases: DEE73 early infantile epileptic encephalopathy 73	C18B12.4	181600	Caenorhabditis elegans	Alliance of Genome Resources
DOID:529	blepharospasm	DRD5	1816	Homo sapiens (human)	Alliance of Genome Resources
DOID:1929	supravalvular aortic stenosis Aliases: Supra-valvular aortic stenosis	csq-1	181563	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2 Aliases: CVPT2	csq-1	181563	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:3633	beta-mannosidosis Aliases: Beta-D-mannosidosis beta-mannosidase deficiency lysosomal beta-mannosidase deficiency	C33G3.4	181517	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10939	antisocial personality disorder Aliases: Asocial personality Dissocial personality disorder Psychopath.personality Psychopathic personality Psychopathic personality disorder sociopathic personality	ABCB1 CACNG8 DRD4 HTR1B	1815 3351 5243 59283	Homo sapiens (human)	Alliance of Genome Resources

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