GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 7101 - 7125 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Homo sapiens (human)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Rattus norvegicus (Norway rat)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Mus musculus (house mouse)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Drosophila melanogaster (fruit fly)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Danio rerio (zebrafish)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Caenorhabditis elegans
DOID:0060673
  • Peters anomaly
Homo sapiens (human)
DOID:0060486
  • Perry syndrome
  • Aliases:
    • parkinsonism with alveolar hypoventilation and mental depression
Homo sapiens (human)
DOID:0050857
  • Perrault syndrome
Homo sapiens (human)
DOID:0060476
  • Perlman syndrome
  • Aliases:
    • nephroblastomatosis - fetal ascites - macrosomia - Wilms tumor
    • nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
    • renal hamartomas, nephroblastomatosis and fetal gigantism
Homo sapiens (human)
DOID:0060744
  • Pendred Syndrome
  • Aliases:
    • TDH2B
    • congenital hypothyroidism due to dyshormonogenesis 2B
    • deafness with goiter
    • genetic defect in thyroid hormonogenesis 2B
    • goiter-deafness syndrome
    • thyroid dyshormonogenesis 2B
Homo sapiens (human)
DOID:3210
  • Pelizaeus-Merzbacher disease
  • Aliases:
    • HLD1
    • Leukodystrophy, sudanophilic
    • PMD
    • Pelizaeus Merzbacher brain sclerosis
    • Pelizaeus-Merzbacher brain sclerosis
    • diffuse familial brain sclerosis
    • hypomyelinating leukodystrophy 1
    • sudanophilic leukodystrophy, Paelizeus-Merzbacher type
Homo sapiens (human)
DOID:9631
  • Pelger-Huet anomaly
Homo sapiens (human)
DOID:0060067
  • Pearson syndrome
  • Aliases:
    • Pearson Marrow-Pancreas Syndrome
Homo sapiens (human)
DOID:11665
  • Patau syndrome
  • Aliases:
    • D1 Trisomy
    • trisomy 13
Homo sapiens (human)
DOID:0080855
  • Parkinsonism
Homo sapiens (human)
DOID:0080855
  • Parkinsonism
Saccharomyces cerevisiae S288C
DOID:0080855
  • Parkinsonism
Caenorhabditis elegans
DOID:0080855
  • Parkinsonism
Rattus norvegicus (Norway rat)
DOID:0080855
  • Parkinsonism
Drosophila melanogaster (fruit fly)
DOID:0080855
  • Parkinsonism
Mus musculus (house mouse)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Caenorhabditis elegans
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Danio rerio (zebrafish)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Xenopus laevis (African clawed frog)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Drosophila melanogaster (fruit fly)

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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: August 19, 2024