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 3951 - 3975 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:9993
  • hypoglycemia
  • Aliases:
    • Hypoglycaemia
Homo sapiens (human)
DOID:10017
  • multiple endocrine neoplasia type 1
  • Aliases:
    • MEN type I
    • Wermer syndrome
    • Wermer's syndrome
Homo sapiens (human)
DOID:0110443
  • dilated cardiomyopathy 1B
Homo sapiens (human)
DOID:5052
  • melioidosis
  • Aliases:
    • Nightcliff gardener's disease
    • Pseudoglanders
    • Whitmore's disease
    • acute and fulminating melioidosis
    • subacute and chronic melioidosis
Homo sapiens (human)
DOID:0110538
  • autosomal recessive nonsyndromic deafness 96
  • Aliases:
    • DFNB96
    • autosomal recessive deafness 96
Homo sapiens (human)
DOID:11482
  • hemopericardium
  • Aliases:
    • Haemopericardium
Homo sapiens (human)
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Homo sapiens (human)
DOID:4330
  • non-Langerhans-cell histiocytosis
Homo sapiens (human)
DOID:12514
  • retinal perforation
  • Aliases:
    • Retinal break
    • Retinal dialysis
    • Retinal tear
Homo sapiens (human)
DOID:3283
  • invasive malignant thymoma
  • Aliases:
    • Infiltrating Thymoma
    • Thymoma malignant Invasive
Homo sapiens (human)
DOID:963
  • episodic ataxia
  • Aliases:
    • Isaacs syndrome
Homo sapiens (human)
DOID:0060655
  • autosomal recessive congenital ichthyosis
  • Aliases:
    • ARCI
    • lamellar ichthyosis
    • non bullous congenital ichthyosiform erythroderma
Homo sapiens (human)
DOID:2347
  • generalized atherosclerosis
  • Aliases:
    • Generalised atherosclerosis
Homo sapiens (human)
DOID:0050527
  • obsolete familial hypertriglyceridemia
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:1803
  • neuritis
  • Aliases:
    • peripheral neuritis
Homo sapiens (human)
DOID:0110513
  • autosomal recessive nonsyndromic deafness 61
  • Aliases:
    • DFNB61
    • autosomal recessive deafness 61
Homo sapiens (human)
DOID:0070210
  • hereditary lymphedema IA
  • Aliases:
    • LMPH1A
Homo sapiens (human)
DOID:0090126
  • branched-chain keto acid dehydrogenase kinase deficiency
  • Aliases:
    • BCKDK deficiency
    • BCKDKD
    • autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
Homo sapiens (human)
DOID:0070122
  • Meckel syndrome 8
  • Aliases:
    • MKS8
    • Meckel-Gruber syndrome, type 8
Homo sapiens (human)
DOID:4367
  • apparent mineralocorticoid excess syndrome
  • Aliases:
    • 11-beta-hydroxysteroid dehydrogenase deficiency type 2
    • Ulick syndrome
    • cortisol 11-beta-ketoreductase deficiency
    • syndrome of apparent mineralocorticoid excess
Homo sapiens (human)
DOID:0110335
  • osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
Homo sapiens (human)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Homo sapiens (human)
DOID:4552
  • large cell carcinoma
Homo sapiens (human)
DOID:0110231
  • cataract 1 multiple types
  • Aliases:
    • CTRCT1
    • Duffy linked cataract
    • cataract 1, multiple types, with or without microcornea
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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