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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 5076 - 5100 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0081395
  • Harel-Yoon syndrome
  • Aliases:
    • Ocular anomalies-axonal neuropathy-developmental delay syndrome
Homo sapiens (human)
DOID:0081396
  • neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome
  • Aliases:
    • PHRINL syndrome
Homo sapiens (human)
DOID:0081397
  • Vissers-Bodmer syndrome
Mus musculus (house mouse)
DOID:0081397
  • Vissers-Bodmer syndrome
Homo sapiens (human)
DOID:0081398
  • holoprosencephaly 12
  • Aliases:
    • holoprosencephaly-12 with or without pancreatic agenesis
Mus musculus (house mouse)
DOID:0081398
  • holoprosencephaly 12
  • Aliases:
    • holoprosencephaly-12 with or without pancreatic agenesis
Homo sapiens (human)
DOID:0081399
  • autosomal dominant distal hereditary motor neuronopathy 10
Homo sapiens (human)
DOID:0081399
  • autosomal dominant distal hereditary motor neuronopathy 10
Mus musculus (house mouse)
DOID:0081400
  • autosomal dominant distal hereditary motor neuronopathy 11
Homo sapiens (human)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Mus musculus (house mouse)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Rattus norvegicus (Norway rat)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Homo sapiens (human)
DOID:0081419
  • childhood-onset dystonia with optic atrophy and basal ganglia abnormalities
  • Aliases:
    • DYSTONIA 29, CHILDHOOD-ONSET
    • DYTOABG
    • MECR-related neurologic disorder
    • MEPAN syndrome
    • Mitochondrial Enoyl CoA Reductase Protein-Associated Neurodegeneration
Homo sapiens (human)
DOID:0081421
  • familial focal epilepsy with variable foci 1
Homo sapiens (human)
DOID:0081421
  • familial focal epilepsy with variable foci 1
Saccharomyces cerevisiae S288C
DOID:0081421
  • familial focal epilepsy with variable foci 1
Mus musculus (house mouse)
DOID:0081423
  • familial focal epilepsy with variable foci 3
Mus musculus (house mouse)
DOID:0081423
  • familial focal epilepsy with variable foci 3
Saccharomyces cerevisiae S288C
DOID:0081423
  • familial focal epilepsy with variable foci 3
Homo sapiens (human)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Homo sapiens (human)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Rattus norvegicus (Norway rat)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Mus musculus (house mouse)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Drosophila melanogaster (fruit fly)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Homo sapiens (human)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024