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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 14376 - 14400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0110220
  • Brugada syndrome 3
  • Aliases:
    • BRGDA3
Homo sapiens (human)
DOID:0070536
  • neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
  • Aliases:
    • NEDHLSS
Homo sapiens (human)
DOID:0060411
  • chromosome 1q21.1 deletion syndrome
  • Aliases:
    • 1q21.1 microdeletion syndrome
Mus musculus (house mouse)
DOID:0081219
  • autosomal recessive intellectual developmental disorder 57
Mus musculus (house mouse)
DOID:0081169
  • Leber congenital amaurosis 19
Mus musculus (house mouse)
DOID:0060352
  • Kleefstra syndrome 1
  • Aliases:
    • 9q subtelomeric deletion syndrome
    • 9q-syndrome
    • 9q34 deletion syndrome
Mus musculus (house mouse)
DOID:0080597
  • Kleefstra syndrome
Mus musculus (house mouse)
DOID:0112205
  • developmental and epileptic encephalopathy 69
  • Aliases:
    • DEE69
    • early infantile epileptic encephalopathy 69
Homo sapiens (human)
DOID:10123
  • pigmentation disease
Danio rerio (zebrafish)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Danio rerio (zebrafish)
DOID:0111725
  • geleophysic dysplasia 1
  • Aliases:
    • GPHYSD1
Mus musculus (house mouse)
DOID:0110871
  • congenital stationary night blindness 2A
  • Aliases:
    • congenital stationary night blindness 2A X-linked
Homo sapiens (human)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Homo sapiens (human)
DOID:0050630
  • Aland Island eye disease
  • Aliases:
    • FORSIUS-ERIKSSON TYPE OCULAR ALBINISM
    • Forsius-Eriksson syndrome
Homo sapiens (human)
DOID:0081350
  • congenital myopathy 18
Homo sapiens (human)
DOID:1826
  • epilepsy
  • Aliases:
    • epilepsy syndrome
    • epileptic syndrome
Xenopus laevis (African clawed frog)
DOID:0060161
  • Kennedy's disease
  • Aliases:
    • Kennedy disease
    • SBMA
    • Spinobulbar Muscular Atrophy
    • X-Linked Bulbo-Spinal Atrophy
    • X-linked Spinal and Bulbar Muscular Atrophy
    • spinal bulbar muscular atrophy
Xenopus laevis (African clawed frog)
DOID:12894
  • Sjogren's syndrome
  • Aliases:
    • Sicca syndrome
    • Sjogren syndrome
    • xerodermosteosis
Xenopus laevis (African clawed frog)
DOID:0080855
  • Parkinsonism
Xenopus laevis (African clawed frog)
DOID:12842
  • Guillain-Barre syndrome
  • Aliases:
    • Infectious neuronitis
    • Post-infectious polyneuritis
    • Postinfectious polyneuritis
    • acute infective polyneuritis
    • acute inflammatory demyelinating polyradiculopathy
    • acute postinfectious polyneuropathy
Xenopus laevis (African clawed frog)
DOID:106
  • pleural tuberculosis
  • Aliases:
    • Pearly disease
    • Tuberculosis of pleura
    • Tuberculous pleurisy
    • Tuberculous pleuritis
    • tuberculous pleurisy in primary progressive tuberculosis
Xenopus laevis (African clawed frog)
DOID:13096
  • Sneddon syndrome
  • Aliases:
    • Idiopathic livedo reticularis with systemic involvement
Xenopus laevis (African clawed frog)
DOID:12798
  • mucopolysaccharidosis
Xenopus laevis (African clawed frog)
DOID:0050778
  • Meckel syndrome
  • Aliases:
    • Meckel-Gruber syndrome
Xenopus laevis (African clawed frog)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Xenopus tropicalis (tropical clawed frog)
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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