GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3751 - 3775 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:11713
  • diabetic angiopathy
  • Aliases:
    • Diabetic vascular disorder
    • diabetic peripheral angiopathy
Mus musculus (house mouse)
DOID:0080759
  • Fanconi renotubular syndrome 3
Homo sapiens (human)
DOID:0111060
  • Ambras type hypertrichosis universalis congenita
  • Aliases:
    • Ambras syndrome
    • HTC1
Homo sapiens (human)
DOID:0111062
  • familial hypobetalipoproteinemia 1
  • Aliases:
    • FHBL1
Homo sapiens (human)
DOID:0060252
  • sclerocornea
  • Aliases:
    • isolated congenital sclerocornea
Homo sapiens (human)
DOID:1386
  • abetalipoproteinemia
  • Aliases:
    • familial hypobetalipoproteinemia
    • microsomal triglyceride transfer protein deficiency disease
Homo sapiens (human)
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Homo sapiens (human)
DOID:1387
  • hypolipoproteinemia
  • Aliases:
    • Hypolipoproteinaemia
Homo sapiens (human)
DOID:0050766
  • choreaacanthocytosis
  • Aliases:
    • Levine-Critchley syndrome
    • choreo-acanthocytosis
Homo sapiens (human)
DOID:1390
  • hypobetalipoproteinemia
  • Aliases:
    • Hypo-beta-lipoproteinemia
Homo sapiens (human)
DOID:1388
  • Tangier disease
  • Aliases:
    • familial alpha-lipoprotein deficiency
    • familial high density lipoprotein deficiency
Homo sapiens (human)
DOID:200
  • benign giant cell tumor
Homo sapiens (human)
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Mus musculus (house mouse)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Danio rerio (zebrafish)
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Danio rerio (zebrafish)
DOID:2978
  • carbohydrate metabolic disorder
  • Aliases:
    • disorder of carbohydrate transport and metabolism
    • inborn carbohydrate metabolism disorder
    • inborn errors of carbohydrate metabolism
Danio rerio (zebrafish)
DOID:162
  • cancer
  • Aliases:
    • malignant neoplasm
    • malignant tumor
    • primary cancer
Danio rerio (zebrafish)
DOID:9282
  • ocular hypertension
Danio rerio (zebrafish)
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Danio rerio (zebrafish)
DOID:612
  • primary immunodeficiency disease
  • Aliases:
    • hypoimmunity
    • immune deficiency disorder
    • immunodeficiency syndrome
Rattus norvegicus (Norway rat)
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Rattus norvegicus (Norway rat)
DOID:0111156
  • spermatogenic failure 9
  • Aliases:
    • globozoospermia
    • male infertility due to round-headed spermatozoa
Caenorhabditis elegans
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Caenorhabditis elegans
DOID:28
  • endocrine system disease
Caenorhabditis elegans
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Caenorhabditis elegans

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024