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 826 - 850 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Saccharomyces cerevisiae S288C
DOID:9252
  • amino acid metabolic disorder
  • Aliases:
    • inborn errors of amino acid metabolism
Saccharomyces cerevisiae S288C
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Saccharomyces cerevisiae S288C
DOID:0060036
  • intrinsic cardiomyopathy
Saccharomyces cerevisiae S288C
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Saccharomyces cerevisiae S288C
DOID:0070539
  • Halperin-Birk syndrome
  • Aliases:
    • HLBKS
    • NEDSOSB
    • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Saccharomyces cerevisiae S288C
DOID:0060559
  • lethal congenital contracture syndrome 1
  • Aliases:
    • LCCS1
    • multiple contracture syndrome, Finnish type
Saccharomyces cerevisiae S288C
DOID:3969
  • thyroid gland papillary carcinoma
  • Aliases:
    • Papillary carcinoma of the Thyroid gland
Saccharomyces cerevisiae S288C
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Saccharomyces cerevisiae S288C
DOID:0060269
  • pontocerebellar hypoplasia type 2C
Saccharomyces cerevisiae S288C
DOID:0080411
  • familial adenomatous polyposis 3
Saccharomyces cerevisiae S288C
DOID:0112380
  • muscular dystrophy-dystroglycanopathy type B2
  • Aliases:
    • MDDGB2
    • congenital muscular dystrophy POMT2-related
Saccharomyces cerevisiae S288C
DOID:0111240
  • congenital muscular dystrophy-dystroglycanopathy type A2
  • Aliases:
    • MDDGA2
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
Saccharomyces cerevisiae S288C
DOID:0110298
  • autosomal recessive limb-girdle muscular dystrophy type 2N
  • Aliases:
    • LGMD2N
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2
    • muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related
Saccharomyces cerevisiae S288C
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Saccharomyces cerevisiae S288C
DOID:0050453
  • lissencephaly
Saccharomyces cerevisiae S288C
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Saccharomyces cerevisiae S288C
DOID:9884
  • muscular dystrophy
Saccharomyces cerevisiae S288C
DOID:0014667
  • disease of metabolism
  • Aliases:
    • metabolic disease
Saccharomyces cerevisiae S288C
DOID:10787
  • premature menopause
  • Aliases:
    • Menopause - premature
    • Menopause praecox
Saccharomyces cerevisiae S288C
DOID:2044
  • drug-induced hepatitis
  • Aliases:
    • Drug-induced chronic hepatitis
Saccharomyces cerevisiae S288C
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Saccharomyces cerevisiae S288C
DOID:1307
  • dementia
Saccharomyces cerevisiae S288C
DOID:0080000
  • muscular disease
Saccharomyces cerevisiae S288C
DOID:423
  • myopathy
Saccharomyces cerevisiae S288C

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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: December 9, 2024