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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 13651 - 13675 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Mus musculus (house mouse)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Caenorhabditis elegans
DOID:0060855
  • autosomal dominant pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1A
    • autosomal dominant PHA 1
Homo sapiens (human)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Rattus norvegicus (Norway rat)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Mus musculus (house mouse)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Caenorhabditis elegans
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Homo sapiens (human)
DOID:0060853
  • Potocki-Lupski syndrome
  • Aliases:
    • 17p11.2 microduplication syndrome
    • chromosome 17p11.2 duplication syndrome
    • trisomy 17p11.2
Homo sapiens (human)
DOID:0060853
  • Potocki-Lupski syndrome
  • Aliases:
    • 17p11.2 microduplication syndrome
    • chromosome 17p11.2 duplication syndrome
    • trisomy 17p11.2
Mus musculus (house mouse)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Drosophila melanogaster (fruit fly)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Homo sapiens (human)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Caenorhabditis elegans
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Mus musculus (house mouse)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Rattus norvegicus (Norway rat)
DOID:0060851
  • pemphigus vulgaris
  • Aliases:
    • familial pemphigus vulgaris
Mus musculus (house mouse)
DOID:0060851
  • pemphigus vulgaris
  • Aliases:
    • familial pemphigus vulgaris
Homo sapiens (human)
DOID:0060850
  • annular pancreas
Caenorhabditis elegans
DOID:0060850
  • annular pancreas
Xenopus tropicalis (tropical clawed frog)
DOID:0060850
  • annular pancreas
Mus musculus (house mouse)
DOID:0060850
  • annular pancreas
Danio rerio (zebrafish)
DOID:0060850
  • annular pancreas
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Mus musculus (house mouse)
DOID:0060848
  • developmental and epileptic encephalopathy 9
  • Aliases:
    • DEE9
    • EFMR
    • EIEE9
    • Juberg Hellman syndrome
    • early infantile epileptic encephalopathy 9
    • early infantile female-limited epilecptic encephalopathy
    • female restricted epilepsy with mental retardation
Mus musculus (house mouse)
DOID:0060848
  • developmental and epileptic encephalopathy 9
  • Aliases:
    • DEE9
    • EFMR
    • EIEE9
    • Juberg Hellman syndrome
    • early infantile epileptic encephalopathy 9
    • early infantile female-limited epilecptic encephalopathy
    • female restricted epilepsy with mental retardation
Danio rerio (zebrafish)
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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