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 551 - 575 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:559
  • acute pyelonephritis
Homo sapiens (human)
DOID:0060655
  • autosomal recessive congenital ichthyosis
  • Aliases:
    • ARCI
    • lamellar ichthyosis
    • non bullous congenital ichthyosiform erythroderma
Homo sapiens (human)
DOID:4591
  • lymphoplasmacyte-rich meningioma
  • Aliases:
    • Lymphoplasmocyte-rich meningioma
Homo sapiens (human)
DOID:12236
  • primary biliary cholangitis
  • Aliases:
    • biliary liver cirrhosis
    • cholestatic cirrhosis
    • chronic nonsuppurative destructive cholangitis
    • primary biliary cirrhosis
Homo sapiens (human)
DOID:8545
  • malignant hyperthermia
  • Aliases:
    • anesthesia related hyperthermia
    • malignant hyperpyrexia due to anesthesia
Homo sapiens (human)
DOID:169
  • neuroendocrine tumor
  • Aliases:
    • neuroendocrine neoplasm
Homo sapiens (human)
DOID:0060605
  • obsolete anterior segment mesenchymal dysgenesis
Homo sapiens (human)
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Homo sapiens (human)
DOID:423
  • myopathy
Homo sapiens (human)
DOID:5348
  • adult endodermal sinus tumor
  • Aliases:
    • adult Yolk Sac neoplasm
    • adult endodermal sinus neoplasm
Homo sapiens (human)
DOID:2378
  • relapsing-remitting multiple sclerosis
  • Aliases:
    • RRMS
    • Relapsing-remitting MS
Homo sapiens (human)
DOID:0060834
  • Griscelli syndrome type 3
  • Aliases:
    • GS3
    • Griscelli-Prunieras syndrome type 3
Homo sapiens (human)
DOID:3369
  • Ewing sarcoma
  • Aliases:
    • Ewing's family localized tumor
    • Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • Ewing's tumor
    • Ewings sarcoma
    • Ewings sarcoma-primitive neuroectodermal tumor
    • PNET of Thoracopulmonary Region
    • localized Ewing sarcoma
    • localized Ewing's sarcoma
    • localized Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • localized Ewing's tumor
    • localized peripheral primitive neuroectodermal tumor
    • peripheral primitive neuroectodermal tumor
Homo sapiens (human)
DOID:0090064
  • familial cold autoinflammatory syndrome 3
Homo sapiens (human)
DOID:0110029
  • alpha thalassemia-intellectual disability syndrome type 1
  • Aliases:
    • ATR syndrome linked to chromosome 16
    • ATR syndrome, deletion type
    • ATR-16 syndrome
    • alpha thalassemia-intellectual disability syndrome, deletion type
    • alpha thalassemia-retardation syndrome
    • alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
    • alpha-thalassemia/mental retardation syndrome, deletion-type
    • alpha-thalassemia/mental retardation syndrome, type 1
Homo sapiens (human)
DOID:3108
  • ascaridiasis
Homo sapiens (human)
DOID:1699
  • obsolete congenital ichthyosiform erythroderma
Homo sapiens (human)
DOID:11983
  • Prader-Willi syndrome
  • Aliases:
    • Prader Willi syndrome
Homo sapiens (human)
DOID:0050834
  • CHARGE syndrome
  • Aliases:
    • CHARGE association
Homo sapiens (human)
DOID:0080476
  • peroxisome biogenesis disorder 1A
  • Aliases:
    • peroxisome biogenesis disorder 1A (Zellweger)
Homo sapiens (human)
DOID:12030
  • panuveitis
  • Aliases:
    • Diffuse uveitis
Homo sapiens (human)
DOID:0050465
  • Muir-Torre syndrome
Homo sapiens (human)
DOID:0110387
  • retinitis pigmentosa 9
  • Aliases:
    • RP9
Homo sapiens (human)
DOID:0110961
  • atypical Gaucher's disease due to saposin c deficiency
Homo sapiens (human)
DOID:12397
  • entropion
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: August 19, 2024