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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 11051 - 11075 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0111160
  • camptodactyly-tall stature-scoliosis-hearing loss syndrome
  • Aliases:
    • CATSHL syndrome
Drosophila melanogaster (fruit fly)
DOID:0111160
  • camptodactyly-tall stature-scoliosis-hearing loss syndrome
  • Aliases:
    • CATSHL syndrome
Homo sapiens (human)
DOID:0111160
  • camptodactyly-tall stature-scoliosis-hearing loss syndrome
  • Aliases:
    • CATSHL syndrome
Xenopus laevis (African clawed frog)
DOID:0090127
  • camptodactyly-arthropathy-coxa vara-pericarditis syndrome
  • Aliases:
    • CACP
    • CACP syndrome
    • CAP syndrome
    • Jacobs syndrome
    • PAC syndrome
    • arthropathy-camptodactyly syndrome
    • camptodactyly-arthropathy-pericarditis syndrome
    • congenital familial hypertrophic synovitis
    • familial fibrosing serositis
    • pericarditis-arthropathy-camptodactyly syndrome
Homo sapiens (human)
DOID:0090127
  • camptodactyly-arthropathy-coxa vara-pericarditis syndrome
  • Aliases:
    • CACP
    • CACP syndrome
    • CAP syndrome
    • Jacobs syndrome
    • PAC syndrome
    • arthropathy-camptodactyly syndrome
    • camptodactyly-arthropathy-pericarditis syndrome
    • congenital familial hypertrophic synovitis
    • familial fibrosing serositis
    • pericarditis-arthropathy-camptodactyly syndrome
Mus musculus (house mouse)
DOID:0050463
  • campomelic dysplasia
  • Aliases:
    • Acampomelic Campomelic Dysplasia
Homo sapiens (human)
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:0080652
  • calcium oxalate nephrolithiasis
Homo sapiens (human)
DOID:0080652
  • calcium oxalate nephrolithiasis
Rattus norvegicus (Norway rat)
DOID:0080652
  • calcium oxalate nephrolithiasis
Mus musculus (house mouse)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Homo sapiens (human)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Drosophila melanogaster (fruit fly)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Mus musculus (house mouse)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Saccharomyces cerevisiae S288C
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Xenopus laevis (African clawed frog)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Caenorhabditis elegans
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Rattus norvegicus (Norway rat)
DOID:11211
  • buphthalmos
  • Aliases:
    • primary congenital glaucoma 3A
    • simple buphthalmos
Homo sapiens (human)
DOID:11211
  • buphthalmos
  • Aliases:
    • primary congenital glaucoma 3A
    • simple buphthalmos
Mus musculus (house mouse)
DOID:11211
  • buphthalmos
  • Aliases:
    • primary congenital glaucoma 3A
    • simple buphthalmos
Caenorhabditis elegans
DOID:8506
  • bullous pemphigoid
Rattus norvegicus (Norway rat)
DOID:8506
  • bullous pemphigoid
Homo sapiens (human)
DOID:8506
  • bullous pemphigoid
Mus musculus (house mouse)
DOID:8506
  • bullous pemphigoid
Danio rerio (zebrafish)
DOID:0060877
  • bullous congenital ichthyosiform erythroderma
  • Aliases:
    • bullous type ichthyosis
    • ichthyosis bullosa of Siemens
    • superficial epidermolytic ichthyosis
Homo sapiens (human)
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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