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 4426 - 4450 of 4621 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0050793
  • short QT syndrome
Homo sapiens (human)
DOID:0050789
  • tarsal-carpal coalition syndrome
Homo sapiens (human)
DOID:0050788
  • proximal symphalangism
  • Aliases:
    • Cushing's symphalangism
Homo sapiens (human)
DOID:0050787
  • juvenile polyposis syndrome
Homo sapiens (human)
DOID:0050785
  • progressive relapsing multiple sclerosis
  • Aliases:
    • PRMS
    • Progressive-relapsing MS
Homo sapiens (human)
DOID:0050784
  • primary progressive multiple sclerosis
  • Aliases:
    • PPMS
    • Primary-progressive MS
Homo sapiens (human)
DOID:0050783
  • secondary progressive multiple sclerosis
  • Aliases:
    • SPMS
    • Secondary-progressive MS
Homo sapiens (human)
DOID:0050782
  • Zollinger-Ellison syndrome
Homo sapiens (human)
DOID:0050780
  • obsolete Opitz-GBBB syndrome
Homo sapiens (human)
DOID:0050778
  • Meckel syndrome
  • Aliases:
    • Meckel-Gruber syndrome
Homo sapiens (human)
DOID:0050777
  • Joubert syndrome
  • Aliases:
    • JBTS
Homo sapiens (human)
DOID:0050776
  • non-syndromic X-linked intellectual disability
  • Aliases:
    • non-specific X-linked mental retardation
Homo sapiens (human)
DOID:0050775
  • schneckenbecken dysplasia
Homo sapiens (human)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Homo sapiens (human)
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Homo sapiens (human)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Homo sapiens (human)
DOID:0050766
  • choreaacanthocytosis
  • Aliases:
    • Levine-Critchley syndrome
    • choreo-acanthocytosis
Homo sapiens (human)
DOID:0050765
  • neuroacanthocytosis
Homo sapiens (human)
DOID:0050763
  • ARC syndrome
  • Aliases:
    • ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS
    • Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome
    • Arthrogryposis-renal dysfunction-cholestasis
Homo sapiens (human)
DOID:0050760
  • X-linked myopathy with excessive autophagy
  • Aliases:
    • XMEA
Homo sapiens (human)
DOID:0050759
  • myotonic dystrophy type 2
Homo sapiens (human)
DOID:0050757
  • deafness-dystonia-optic neuronopathy syndrome
  • Aliases:
    • Deafness Dystonia Optic Atrophy Syndrome
    • Deafness Dystonia Optic Neuronopathy Syndrome
    • Dystonia Deafness Syndrome
    • Jensen syndrome
    • Mohr-Tranebjaerg syndrome
    • deafness dystonia syndrome
Homo sapiens (human)
DOID:0050754
  • ataxia with oculomotor apraxia type 1
Homo sapiens (human)
DOID:0050753
  • cerebellar ataxia
Homo sapiens (human)
DOID:0050749
  • peripheral T-cell lymphoma
Homo sapiens (human)

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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