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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 **9976 - 10000** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:589	congenital hemolytic anemia Aliases: congenital hemolytic anaemia hereditary hemolytic anaemia hereditary hemolytic anemia	abts-4	180943	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:12971	hereditary spherocytosis Aliases: Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia	abts-4	180943	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110919	hereditary spherocytosis type 4 Aliases: HS4 SPH4 hereditary spherocytosis 4	abts-4	180943	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2373	hereditary elliptocytosis Aliases: Congenital elliptocytosis ovalocytosis	abts-4	180943	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8618	oral cavity cancer Aliases: malignant neoplasm of floor of mouth	acr-3	180937	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12176	goiter Aliases: goitre	svh-2	180929	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050437	Danon disease Aliases: ANTOPOL DISEASE PSEUDOGLYCOGENOSIS II	lmp-1	180912	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	lmp-1	180912	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060496	respiratory allergy Aliases: airway allergy	gnrr-4	180841	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110705	hypotrichosis 8 Aliases: Hypt8 Lah3 hypotrichosis, localized, autosomal recessive 3	gnrr-4	180841	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070490	infantile parkinsonism-dystonia 2 Aliases: Brain dopamine-serotonin vesicular transport disease PKDYS2	cat-1	180837	Caenorhabditis elegans	Alliance of Genome Resources
DOID:303	substance-related disorder	cat-1	180837	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1440	Machado-Joseph disease Aliases: Azorean disease MJD SCA3 spinocerebellar ataxia 3 spinocerebellar ataxia type 3	cat-1	180837	Caenorhabditis elegans	Alliance of Genome Resources
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	W01C8.5	180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111908	thrombophilia due to thrombomodulin defect Aliases: THBD-related bleeding disorder THBD-related coagulopathy THPH12 thrombomodulin-related bleeding disorder thrombomodulin-related coagulopathy	W01C8.5	180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3410	carotid artery thrombosis	W01C8.5	180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2452	thrombophilia Aliases: hypercoagulability state	W01C8.5	180836	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112313	brain small vessel disease	W01C8.5 lev-9	180836 188252	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080301	atypical hemolytic-uremic syndrome	W01C8.5 cfh-1	180836 185381	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070030	ITM2B-related cerebral amyloid angiopathy 2 Aliases: Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis FDD Familial Danish Dementia HOOE Heredopathia Ophthalmootoencephalica	itm-2	180816	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1 Aliases: Cerebral Amyloid Angiopathy, British Type FBD Familial British Dementia Presenile Dementia with Spastic Ataxia	itm-2	180816	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9246	cerebral amyloid angiopathy Aliases: Cerebral Hemorrhage, Hereditary, with Amyloidosis Hereditary Cerebral Hemorrhage with Amyloidosis	itm-2 nep-2	180816 188090	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080268	autosomal dominant nonsyndromic deafness 72	chtl-1	180809	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081097	Rafiq syndrome Aliases: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15	mans-3	180787	Caenorhabditis elegans	Alliance of Genome Resources

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