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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 7051 - 7075 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0080329
  • cold-induced sweating syndrome 1
Homo sapiens (human)
DOID:0070229
  • intrahepatic cholestasis of pregnancy 3
  • Aliases:
    • ICP3
    • pregnancy related cholestasis 3
Homo sapiens (human)
DOID:0080410
  • familial adenomatous polyposis 2
  • Aliases:
    • MUTYH-associated polyposis
    • MUTYH-related attenuated FAP
    • MUTYH-related attenuated familial adenomatous polyposis
    • MUTYH-related attenuated familial polyposis coli
Homo sapiens (human)
DOID:0080986
  • Ehlers-Danlos syndrome periodontal type 1
Homo sapiens (human)
DOID:0110245
  • cataract 38
  • Aliases:
    • CATC5
    • CTRCT38
    • autosomal recessive congenital cataract 5
Homo sapiens (human)
DOID:9778
  • irritable bowel syndrome
  • Aliases:
    • IBD
    • Irritable colon
Homo sapiens (human)
DOID:484
  • vascular hemostatic disease
Homo sapiens (human)
DOID:11111
  • hydronephrosis
Homo sapiens (human)
DOID:12978
  • Plasmodium vivax malaria
  • Aliases:
    • Malaria by Plasmodium vivax
    • Vivax Malaria
Homo sapiens (human)
DOID:2962
  • Cockayne syndrome
  • Aliases:
    • Neill-Dingwall syndrome
Homo sapiens (human)
DOID:0111669
  • hyaline fibromatosis syndrome
  • Aliases:
    • HFS
    • inherited systemic hyalinosis
    • puretic syndrome
    • systemic hyalinosis
Homo sapiens (human)
DOID:0110993
  • Joubert syndrome 24
  • Aliases:
    • JBTS24
Homo sapiens (human)
DOID:0111169
  • subcortical band heterotopia
  • Aliases:
    • HeCo
    • band heterotopia
    • double cortex syndrome
    • heterotopic cortex
    • subcortical laminar heterotopia
Homo sapiens (human)
DOID:0111305
  • familial febrile seizures 4
  • Aliases:
    • FEB4
    • familial febrile convulsions 4
Homo sapiens (human)
DOID:6846
  • familial melanoma
Homo sapiens (human)
DOID:12206
  • dengue hemorrhagic fever
  • Aliases:
    • DHF
Homo sapiens (human)
DOID:0081124
  • craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1
Homo sapiens (human)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Homo sapiens (human)
DOID:0070283
  • primary autosomal recessive microcephaly 13
  • Aliases:
    • MCPH13
Homo sapiens (human)
DOID:0112329
  • pontocerebellar hypoplasia type 2F
  • Aliases:
    • PCH2F
Homo sapiens (human)
DOID:11162
  • respiratory failure
  • Aliases:
    • acute and chronic respiratory failure
    • acute respiratory Failure
    • acute-on-chronic respiratory failure
    • chronic respiratory failure
    • respiratory insufficiency/failure
Homo sapiens (human)
DOID:0110347
  • osteogenesis imperfecta type 15
  • Aliases:
    • OI15
    • osteogenesis imperfecta type XV
Homo sapiens (human)
DOID:0060309
  • syndromic X-linked intellectual disability
  • Aliases:
    • syndromic X-linked mental retardation
Homo sapiens (human)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Homo sapiens (human)
DOID:0110883
  • inflammatory bowel disease 17
  • Aliases:
    • IBD17
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