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 1826 - 1850 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110245
  • cataract 38
  • Aliases:
    • CATC5
    • CTRCT38
    • autosomal recessive congenital cataract 5
Homo sapiens (human)
DOID:1210
  • optic neuritis
Homo sapiens (human)
DOID:4310
  • smooth muscle tumor
Homo sapiens (human)
DOID:0080211
  • nodal marginal zone lymphoma
Homo sapiens (human)
DOID:9169
  • Wiskott-Aldrich syndrome
  • Aliases:
    • Wiskott syndrome
Homo sapiens (human)
DOID:0060340
  • ciliopathy
Homo sapiens (human)
DOID:589
  • congenital hemolytic anemia
  • Aliases:
    • congenital hemolytic anaemia
    • hereditary hemolytic anaemia
    • hereditary hemolytic anemia
Homo sapiens (human)
DOID:13603
  • obstructive jaundice
  • Aliases:
    • Cholestatic Jaundice
    • Cholestatic jaundice syndrome
    • Obstructive hyperbilirubinemia
Homo sapiens (human)
DOID:0110257
  • cataract 24
  • Aliases:
    • CTRCT24
Homo sapiens (human)
DOID:0112275
  • developmental and epileptic encephalopathy 93
  • Aliases:
    • DEE93
    • IECEE3
    • infantile or early childhood epileptic encephalopathy 3
Homo sapiens (human)
DOID:0110805
  • hereditary spastic paraplegia 53
  • Aliases:
    • SPG53
    • autosomal recessive spastic paraplegia 53
    • autosomal recessive spastic paraplegia type 53
Homo sapiens (human)
DOID:5268
  • myxoid leiomyosarcoma
Homo sapiens (human)
DOID:12328
  • marasmus
  • Aliases:
    • Nutritional atrophy
    • Nutritional marasmus
Homo sapiens (human)
DOID:12273
  • anisometropia
Homo sapiens (human)
DOID:2234
  • focal epilepsy
  • Aliases:
    • localisation-related epilepsy
    • partial epilepsy
Homo sapiens (human)
DOID:96
  • staphyloenterotoxemia
  • Aliases:
    • Staphylococcal food poisoning
    • Staphylococcal toxaemia due to food
    • staphyloenterotoxicosis
Homo sapiens (human)
DOID:3168
  • squamous cell neoplasm
  • Aliases:
    • Epidermoid cell tumor
    • squamous cell tumor
Homo sapiens (human)
DOID:0080556
  • congenital disorder of glycosylation Id
  • Aliases:
    • congenital disorder of glycosylation 1d
Homo sapiens (human)
DOID:0002116
  • pterygium
  • Aliases:
    • surfer's eye
Homo sapiens (human)
DOID:10375
  • strabismic amblyopia
  • Aliases:
    • suppression amblyopia
Homo sapiens (human)
DOID:9883
  • Becker muscular dystrophy
  • Aliases:
    • Benign pseudohypertrophic muscular dystrophy
    • benign congenital myopathy
Homo sapiens (human)
DOID:3119
  • gastrointestinal system cancer
  • Aliases:
    • GI tumor
    • digestive system cancer
    • gastrointestinal tract cancer
Homo sapiens (human)
DOID:0050437
  • Danon disease
  • Aliases:
    • ANTOPOL DISEASE
    • PSEUDOGLYCOGENOSIS II
Homo sapiens (human)
DOID:7400
  • Nijmegen breakage syndrome
  • Aliases:
    • Berlin breakage syndrome
    • Microcephaly, normal intelligence and immunodeficiency
    • NBS
    • Seemanova syndrome II
    • Seemanova syndrome type 2
    • ataxia-telangiectasia variant
    • immunodeficiency-microcephaly-chromosomal instability syndrome
    • microcephaly-immunodeficiency-lymphoreticuloma syndrome
Homo sapiens (human)
DOID:0090093
  • hypogonadotropic hypogonadism 21 with or without anosmia
Homo sapiens (human)

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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