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 5701 - 5725 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:8432
  • polycythemia
  • Aliases:
    • Erythrocythemia
Mus musculus (house mouse)
DOID:0111730
  • familial episodic pain syndrome 2
  • Aliases:
    • FEPS2
Mus musculus (house mouse)
DOID:987
  • alopecia
Mus musculus (house mouse)
DOID:0111242
  • congenital muscular dystrophy-dystroglycanopathy type A6
  • Aliases:
    • MDDGA6
    • Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6
Mus musculus (house mouse)
DOID:0080291
  • developmental and epileptic encephalopathy 59
  • Aliases:
    • DEE59
    • early infantile epileptic encephalopathy 59
Mus musculus (house mouse)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Mus musculus (house mouse)
DOID:8584
  • Burkitt lymphoma
  • Aliases:
    • Burkitt lymphoma/leukaemia
    • Burkitt's Lymphoma
    • Burkitt's tumor
    • Burkitt's tumor or lymphoma
    • malignant lymphoma, Burkitt's type
    • small Non-Cleaved cell Lymphoma, Burkitt's type
Mus musculus (house mouse)
DOID:10966
  • lipoid nephrosis
  • Aliases:
    • Minimal Change Glomerulonephritis
    • Minimal change disease
    • Nephrotic syndrome with lesion of minimal change glomerulonephritis
    • Nephrotic syndrome with lesion of minimal change nephrotic syndrome
Mus musculus (house mouse)
DOID:0111059
  • Bernard-Soulier syndrome type A2
  • Aliases:
    • BSSA2
Mus musculus (house mouse)
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Mus musculus (house mouse)
DOID:0110079
  • Leber congenital amaurosis 8
  • Aliases:
    • LCA8
Mus musculus (house mouse)
DOID:0080338
  • familial erythrocytosis 3
  • Aliases:
    • ECYT3
Mus musculus (house mouse)
DOID:0060674
  • catecholaminergic polymorphic ventricular tachycardia
Mus musculus (house mouse)
DOID:0111260
  • phosphoribosylpyrophosphate synthetase superactivity
  • Aliases:
    • PRPP synthetase superactivity
    • PRPS1 superactivity
Mus musculus (house mouse)
DOID:0081319
  • multiple synostoses syndrome 3
Mus musculus (house mouse)
DOID:0111664
  • ectodermal dysplasia 1
  • Aliases:
    • CST syndrome
    • Christ-Siemens-Touraine syndrome
    • ED1
    • HED1
    • X-linked anhidrotic ectodermal dysplasia
    • XHED
    • XLHED
    • ectodermal dysplasia 1, anhidrotic
    • ectodermal dysplasia 1, hypohidrotic, X-linked
    • ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked
    • hypohidrotic ectodermal dysplasia, X-Linked
Mus musculus (house mouse)
DOID:4159
  • skin cancer
  • Aliases:
    • CA - skin cancer
    • malignant neoplasm of skin
    • melanoma and Non-melanoma skin cancer
Mus musculus (house mouse)
DOID:9507
  • ethmoid sinusitis
  • Aliases:
    • ethmoidal sinusitis
    • ethmoiditis
Mus musculus (house mouse)
DOID:0110734
  • neurodegeneration with brain iron accumulation
  • Aliases:
    • NBIA
Mus musculus (house mouse)
DOID:0080743
  • transverse myelitis
Mus musculus (house mouse)
DOID:12205
  • dengue disease
  • Aliases:
    • Dengue Fever
    • breakbone fever
    • classic dengue
Mus musculus (house mouse)
DOID:0060757
  • sclerosteosis 2
  • Aliases:
    • SOST2
Mus musculus (house mouse)
DOID:0070309
  • absence epilepsy
Mus musculus (house mouse)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Mus musculus (house mouse)
DOID:9274
  • hyperlysinemia
Mus musculus (house mouse)

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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