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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 3451 - 3475 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:11166
  • Human papillomavirus infectious disease
  • Aliases:
    • HPV
Saccharomyces cerevisiae S288C
DOID:0111019
  • cone-rod dystrophy 12
  • Aliases:
    • CORD12
Caenorhabditis elegans
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Danio rerio (zebrafish)
DOID:0060334
  • transient neonatal diabetes mellitus
Rattus norvegicus (Norway rat)
DOID:0111467
  • combined oxidative phosphorylation deficiency 13
  • Aliases:
    • COXPD13
Mus musculus (house mouse)
DOID:401
  • multidrug-resistant tuberculosis
Homo sapiens (human)
DOID:0111457
  • STING-associated vasculopathy with onset in infancy
  • Aliases:
    • SAVI
Homo sapiens (human)
DOID:869
  • cholesteatoma
Caenorhabditis elegans
DOID:12336
  • male infertility
Danio rerio (zebrafish)
DOID:0050650
  • familial atrial fibrillation
  • Aliases:
    • ATFB
Homo sapiens (human)
DOID:0050566
  • X-linked nonsyndromic deafness
  • Aliases:
    • X-linked deafness
Homo sapiens (human)
DOID:10303
  • sialadenitis
  • Aliases:
    • Sialoadenitis
Mus musculus (house mouse)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Homo sapiens (human)
DOID:14219
  • renal tubular acidosis
Rattus norvegicus (Norway rat)
DOID:0060936
  • dystonia 28 childhood-onset
  • Aliases:
    • DYSTONIA 28, CHILDHOOD-ONSET
    • DYT28
Mus musculus (house mouse)
DOID:0090018
  • autosomal dominant familial periodic fever
  • Aliases:
    • FHF
    • FPF
    • TNF receptor associated periodic syndrome
    • TRAPS
    • familial Hibernian fever
    • hibernian fever
    • tumor necrosis factor receptor associated periodic syndrome
Homo sapiens (human)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Rattus norvegicus (Norway rat)
DOID:3717
  • gastric adenocarcinoma
  • Aliases:
    • adenocarcinoma of stomach
    • stomach adenocarcinoma
Caenorhabditis elegans
DOID:070355
  • multisystem proteinopathy
Mus musculus (house mouse)
DOID:0111196
  • X-linked distal spinal muscular atrophy 3
  • Aliases:
    • ATP7A-related distal motor neuropathy
    • DSMAX
    • SMAX3
    • X-linked dHMN3
    • X-linked dSMA3
    • X-linked distal hereditary motor neuropathy type 3
    • X-linked recessive distal spinal muscular atrophy
Mus musculus (house mouse)
DOID:0080625
  • severe congenital neutropenia 1
Homo sapiens (human)
DOID:12510
  • retinal ischemia
Mus musculus (house mouse)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Mus musculus (house mouse)
DOID:0060211
  • amyotrophic lateral sclerosis type 20
  • Aliases:
    • ALS20
    • amyotrophic lateral sclerosis 20
Mus musculus (house mouse)
DOID:0111046
  • platelet-type bleeding disorder 10
  • Aliases:
    • BDPLT10
    • CD36 deficiency
    • platelet glycoprotein IV deficiency
Caenorhabditis elegans
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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