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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 2376 - 2400 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0080957
  • primary hypoalphalipoproteinemia 1
  • Aliases:
    • familial HDL deficiency
    • familial hypoalphalipoproteinemia
Mus musculus (house mouse)
DOID:14283
  • primary hypertrophic osteoarthropathy
  • Aliases:
    • Pachydermoperiostosis of nail
    • Pachydermoperiostosis syndrome
Homo sapiens (human)
DOID:14283
  • primary hypertrophic osteoarthropathy
  • Aliases:
    • Pachydermoperiostosis of nail
    • Pachydermoperiostosis syndrome
Mus musculus (house mouse)
DOID:2977
  • primary hyperoxaluria
Mus musculus (house mouse)
DOID:2977
  • primary hyperoxaluria
Homo sapiens (human)
DOID:0111672
  • primary hyperoxaluria type 3
  • Aliases:
    • HP3
    • PH III
    • primary hyperoxaluria type III
Homo sapiens (human)
DOID:0111671
  • primary hyperoxaluria type 2
  • Aliases:
    • D-glycerate dehydrogenase deficiency
    • HP2
    • L-glyceric aciduria
    • glyoxylate reductase/hydroxypyruvate reductase deficiency
    • oxalosis II
Mus musculus (house mouse)
DOID:0111671
  • primary hyperoxaluria type 2
  • Aliases:
    • D-glycerate dehydrogenase deficiency
    • HP2
    • L-glyceric aciduria
    • glyoxylate reductase/hydroxypyruvate reductase deficiency
    • oxalosis II
Homo sapiens (human)
DOID:0111670
  • primary hyperoxaluria type 1
  • Aliases:
    • HP1
    • alanine-glyoxylate aminotransferase deficiency
    • glycolic aciduria
    • hepatic AGT deficiency
    • oxalosis I
    • peroxisomal alanine-glyoxylate aminotransferase deficiency
    • serine pyruvate aminotransferase deficiency
Homo sapiens (human)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Caenorhabditis elegans
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Danio rerio (zebrafish)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Drosophila melanogaster (fruit fly)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Homo sapiens (human)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Saccharomyces cerevisiae S288C
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Mus musculus (house mouse)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Rattus norvegicus (Norway rat)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Mus musculus (house mouse)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Caenorhabditis elegans
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Rattus norvegicus (Norway rat)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Homo sapiens (human)
DOID:0050639
  • primary cutaneous amyloidosis
  • Aliases:
    • PCA
    • familial primary localized cutaneous amyloidosis
Homo sapiens (human)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Homo sapiens (human)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Mus musculus (house mouse)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Rattus norvegicus (Norway rat)
DOID:0050593
  • primary congenital glaucoma
Homo sapiens (human)
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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