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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 1776 - 1800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0050605
  • acrodermatitis enteropathica
Mus musculus (house mouse)
DOID:0111836
  • congenital nongoitrous hypothyroidism 7
  • Aliases:
    • CHNG7
    • TRH resistance syndrome
    • central hypothyroidism due to TRH receptor deficiency
    • resistance to thyrotropin-releasing hormone syndrome
Homo sapiens (human)
DOID:0060297
  • complement component 4a deficiency
Homo sapiens (human)
DOID:0050871
  • fibroma
Mus musculus (house mouse)
DOID:7427
  • anthrax disease
Mus musculus (house mouse)
DOID:0111669
  • hyaline fibromatosis syndrome
  • Aliases:
    • HFS
    • inherited systemic hyalinosis
    • puretic syndrome
    • systemic hyalinosis
Mus musculus (house mouse)
DOID:0070405
  • hypomyelinating leukodystrophy 16
  • Aliases:
    • HLD16
Mus musculus (house mouse)
DOID:0070238
  • primary coenzyme Q10 deficiency 1
  • Aliases:
    • COQ10D1
    • CoQ deficiency 1
    • CoQ10 deficiency, primary, 1
    • coenzyme Q deficiency 1
    • ubiquinone deficiency 1
Mus musculus (house mouse)
DOID:0112312
  • male infertility due to globozoospermia
  • Aliases:
    • globozoospermia syndrome
Homo sapiens (human)
DOID:0111399
  • congenital dyserythropoietic anemia type III
  • Aliases:
    • CDA III
    • CDA type 3
    • CDA type III
    • CDAN3
    • Congenital dyserythropoietic anaemia type 3
    • Congenital dyserythropoietic anemia type 3
    • anaemia with multinucleated erythroblasts
    • anemia with multinucleated erythroblasts
    • congenital dyserythropoietic anaemia type III
    • hereditary benign erythroreticulosis
Mus musculus (house mouse)
DOID:0110021
  • age related macular degeneration 9
  • Aliases:
    • ARMD9
Homo sapiens (human)
DOID:5162
  • arteriolosclerosis
Homo sapiens (human)
DOID:8354
  • complement component 3 deficiency
  • Aliases:
    • C3 deficiency
Homo sapiens (human)
DOID:0112186
  • thyroid dyshormonogenesis 2A
  • Aliases:
    • TDH2A
    • genetic defect in thyroid hormonogenesis 2A
    • iodide peroxidase deficiency
    • thyroid peroxidase deficiency
Homo sapiens (human)
DOID:0080236
  • autosomal dominant intellectual developmental disorder 45
  • Aliases:
    • autosomal dominant mental retardation 45
Mus musculus (house mouse)
DOID:0110521
  • autosomal recessive nonsyndromic deafness 70
  • Aliases:
    • DFNB70
    • autosomal recessive deafness 70
Mus musculus (house mouse)
DOID:0050974
  • spinocerebellar ataxia type 25
Mus musculus (house mouse)
DOID:0111467
  • combined oxidative phosphorylation deficiency 13
  • Aliases:
    • COXPD13
Mus musculus (house mouse)
DOID:0060295
  • complement component 2 deficiency
Homo sapiens (human)
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Homo sapiens (human)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Mus musculus (house mouse)
DOID:10930
  • borderline personality disorder
Homo sapiens (human)
DOID:0080987
  • Ehlers-Danlos syndrome periodontal type 2
Homo sapiens (human)
DOID:0060412
  • chromosome 1q41-q42 deletion syndrome
  • Aliases:
    • 1q41-q42 microdeletion syndrome
    • 1q41q42 microdeletion syndrome
Homo sapiens (human)
DOID:3012
  • Li-Fraumeni syndrome
  • Aliases:
    • LFS
    • Li-Fraumeni Familiar cancer Susceptibility syndrome
    • SBLA syndrome
    • sarcoma, breast, leukaemia and adrenal gland syndrome
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: December 9, 2024