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 3801 - 3825 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:8527
  • monocytic leukemia
  • Aliases:
    • Schilling's leukaemia
    • Schilling's leukemia
    • monocytic leukaemia
Homo sapiens (human)
DOID:12550
  • hepatic coma
  • Aliases:
    • Hepatocerebral intoxication
Homo sapiens (human)
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Homo sapiens (human)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Homo sapiens (human)
DOID:2033
  • communication disorder
Homo sapiens (human)
DOID:93
  • language disorder
Homo sapiens (human)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:5847
  • posterior myocardial infarction
Homo sapiens (human)
DOID:0110912
  • leukocyte adhesion deficiency 3
  • Aliases:
    • IADD
    • LAD1 variant
    • LAD1V
    • LAD3
    • integrin activation deficiency disease
    • leukocyte adhesion deficiency 1 variant
    • leukocyte adhesion deficiency type III
Homo sapiens (human)
DOID:0110669
  • congenital myasthenic syndrome 14
  • Aliases:
    • CMS14
    • CMSTA3
    • congenital myasthenic syndrome 14, with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 3
Caenorhabditis elegans
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Caenorhabditis elegans
DOID:10763
  • hypertension
  • Aliases:
    • HTN
    • hyperpiesia
    • vascular hypertensive disorder
Caenorhabditis elegans
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Caenorhabditis elegans
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Caenorhabditis elegans
DOID:0070112
  • Niemann-Pick disease type B
Caenorhabditis elegans
DOID:0070111
  • Niemann-Pick disease type A
Caenorhabditis elegans
DOID:0050775
  • schneckenbecken dysplasia
Caenorhabditis elegans
DOID:0070311
  • oligoasthenoteratozoospermia
  • Aliases:
    • OAT
    • oligoasthenoteratospermia
Caenorhabditis elegans
DOID:0060713
  • autosomal recessive congenital ichthyosis 4B
  • Aliases:
    • ARCI4B
    • harlequin ichthyosis
    • harlequin type ichthyosis congenita
    • harlequin type ichthyosis fetalis
Caenorhabditis elegans
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
Caenorhabditis elegans
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Caenorhabditis elegans
DOID:10652
  • Alzheimer's disease
  • Aliases:
    • Alzheimer disease
    • Alzheimers dementia
Caenorhabditis elegans
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Caenorhabditis elegans
DOID:0080855
  • Parkinsonism
Caenorhabditis elegans
DOID:936
  • brain disease
  • Aliases:
    • encephalopathy
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