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 9076 - 9100 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:7166
  • thyroiditis
Mus musculus (house mouse)
DOID:0080460
  • developmental and epileptic encephalopathy 34
  • Aliases:
    • DEE34
    • early infantile epileptic encephalopathy 34
Mus musculus (house mouse)
DOID:0080612
  • anterior segment dysgenesis 7
Mus musculus (house mouse)
DOID:0080502
  • GM1 gangliosidosis type 1
Mus musculus (house mouse)
DOID:3008
  • invasive ductal carcinoma
  • Aliases:
    • Infiltrating ductal carcinoma of breast
    • Invasive ductal carcinoma, NST
    • ductal adenocarcinoma
Mus musculus (house mouse)
DOID:0060676
  • catecholaminergic polymorphic ventricular tachycardia 2
  • Aliases:
    • CVPT2
Mus musculus (house mouse)
DOID:0080743
  • transverse myelitis
Mus musculus (house mouse)
DOID:0050824
  • sinoatrial node disease
  • Aliases:
    • SA node
    • sinuatrial node
Mus musculus (house mouse)
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Mus musculus (house mouse)
DOID:0110825
  • hereditary spastic paraplegia 9B
  • Aliases:
    • SPG9B
    • autosomal recessive complex spastic paraplegia type 9B
    • autosomal recessive spastic paraplegia 9B
Mus musculus (house mouse)
DOID:1749
  • squamous cell carcinoma
  • Aliases:
    • epidermoid carcinoma
    • malignant squamous cell tumor
    • squamous carcinoma
    • squamous cell Epithelioma
    • squamous cell cancer
Mus musculus (house mouse)
DOID:9884
  • muscular dystrophy
Mus musculus (house mouse)
DOID:0080195
  • Marinesco-Sjogren syndrome
  • Aliases:
    • Garland-Moorhouse syndrome
    • Marinesco-Garland syndrome
    • Oligophrenic cerebellolenticular degeneration
    • hereditary oligophrenic cerebello-lental degeneration
Mus musculus (house mouse)
DOID:0111815
  • low molecular weight proteinuria with hypercalciuric nephrocalcinosis
Mus musculus (house mouse)
DOID:0070035
  • autosomal dominant intellectual developmental disorder 5
  • Aliases:
    • MRD5
    • autosomal dominant mental retardation 5
    • autosomal dominant non-syndromic intellectual disability 5
Mus musculus (house mouse)
DOID:0110336
  • osteogenesis imperfecta type 8
  • Aliases:
    • OI8
    • osteogenesis imperfecta type VIII
Mus musculus (house mouse)
DOID:77
  • gastrointestinal system disease
  • Aliases:
    • GIT disease
    • Gastroenteropathy
    • alimentary system disease
    • digestive system disorder
    • gastrointestinal disease
    • gastrointestinal disorder
Mus musculus (house mouse)
DOID:12987
  • agranulocytosis
  • Aliases:
    • Granulocytopenic disorder
    • Granulopenia
    • granulocytopenia
Mus musculus (house mouse)
DOID:0081343
  • congenital myopathy 9A
Mus musculus (house mouse)
DOID:0080720
  • autosomal dominant congenital deafness with onychodystrophy
Mus musculus (house mouse)
DOID:0070036
  • autosomal dominant intellectual developmental disorder 6
  • Aliases:
    • MRD6
    • autosomal dominant mental retardation 6
    • autosomal dominant non-syndromic intellectual disability 6
Mus musculus (house mouse)
DOID:0060575
  • 3MC syndrome 1
Mus musculus (house mouse)
DOID:0081385
  • ataxia-telangiectasia-like disorder-2
  • Aliases:
    • PCNA-related progressive neurodegenerative photosensitivity syndrome
Mus musculus (house mouse)
DOID:0110357
  • retinitis pigmentosa 35
  • Aliases:
    • RP35
Mus musculus (house mouse)
DOID:0060750
  • familial temporal lobe epilepsy 3
  • Aliases:
    • FMTLE
    • familial mesial temporal lobe epilepsy
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