Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
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 1851 - 1875 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080067
  • Charcot-Marie-Tooth disease type 5
  • Aliases:
    • hereditary motor and sensory neuropathy with pyramidal features
Homo sapiens (human)
DOID:0110809
  • hereditary spastic paraplegia 57
  • Aliases:
    • SPG57
    • autosomal recessive spastic paraplegia 57
    • autosomal recessive spastic paraplegia type 57
Homo sapiens (human)
DOID:0110813
  • hereditary spastic paraplegia 62
  • Aliases:
    • SPG62
    • autosomal recessive spastic paraplegia 62
    • autosomal recessive spastic paraplegia type 62
Homo sapiens (human)
DOID:0110789
  • hereditary spastic paraplegia 38
  • Aliases:
    • SPG38
    • autosomal dominant spastic paraplegia 38
    • autosomal dominant spastic paraplegia type 38
Homo sapiens (human)
DOID:0110811
  • hereditary spastic paraplegia 6
  • Aliases:
    • FSP3
    • SPG6
    • autosomal dominant familial spastic paraplegia type 3
    • autosomal dominant spastic paraplegia 6
    • autosomal dominant spastic paraplegia type 6
Homo sapiens (human)
DOID:0110788
  • hereditary spastic paraplegia 37
  • Aliases:
    • SPG37
    • autosomal dominant spastic paraplegia 37
    • autosomal dominant spastic paraplegia type 37
Homo sapiens (human)
DOID:0110781
  • hereditary spastic paraplegia 30
  • Aliases:
    • SPG30
    • autosomal spastic paraplegia type 30
Homo sapiens (human)
DOID:0110778
  • hereditary spastic paraplegia 27
  • Aliases:
    • SPG27
    • autosomal recessive spastic paraplegia 27
    • autosomal recessive spastic paraplegia type 27
Homo sapiens (human)
DOID:0110792
  • hereditary spastic paraplegia 4
  • Aliases:
    • SPG4
    • autosomal dominant spastic paraplegia 4
    • autosomal dominant spastic paraplegia type 4
Homo sapiens (human)
DOID:0110779
  • hereditary spastic paraplegia 28
  • Aliases:
    • SPG28
    • autosomal recessive spastic paraplegia 28
    • autosomal recessive spastic paraplegia type 28
Homo sapiens (human)
DOID:0110791
  • hereditary spastic paraplegia 3A
  • Aliases:
    • FSP1
    • SPG3A
    • autosomal dominant familial spastic paraplegia 1
    • autosomal dominant spastic paraplegia 3
    • autosomal dominant spastic paraplegia type 3
    • strumpell disease
Homo sapiens (human)
DOID:0110790
  • hereditary spastic paraplegia 39
  • Aliases:
    • NTE-related motor neuron disorder
    • NTEMND
    • SPG39
    • autosomal recessive spastic paraplegia 39
    • autosomal recessive spastic paraplegia type 39
    • spastic paraplegia due to NTE mutation
    • spastic paraplegia due to neuropathy target esterase mutation
Homo sapiens (human)
DOID:0110824
  • hereditary spastic paraplegia 9A
  • Aliases:
    • AD-SPG9A
    • Cataracts motor neuropathy-short stature-skeletal anomalies syndrome
    • SPG9A
    • autosomal dominant complex spastic paraplegia type 9A
    • autosomal dominant spastic paraplegia 9A
    • cataracts with motor neuronopathy, short stature and skeletal abnormalities
    • spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
    • spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
Homo sapiens (human)
DOID:0110765
  • hereditary spastic paraplegia 12
  • Aliases:
    • SPG12
    • autosomal dominant spastic paraplegia 12
    • autosomal dominant spastic paraplegia type 12
Homo sapiens (human)
DOID:0110769
  • hereditary spastic paraplegia 16
  • Aliases:
    • SPG16
    • X-linked spastic paraplegia 16
    • X-linked spastic paraplegia type 16
Homo sapiens (human)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Homo sapiens (human)
DOID:0110794
  • hereditary spastic paraplegia 42
  • Aliases:
    • SPG42
    • autosomal dominant spastic paraplegia 42
    • autosomal dominant spastic paraplegia type 42
Homo sapiens (human)
DOID:0110795
  • hereditary spastic paraplegia 43
  • Aliases:
    • SPG43
    • autosomal recessive spastic paraplegia 43
    • autosomal recessive spastic paraplegia type 43
Homo sapiens (human)
DOID:0110775
  • hereditary spastic paraplegia 24
  • Aliases:
    • SPG24
    • autosomal recessive spastic paraplegia 24
    • autosomal recessive spastic paraplegia type 24
Homo sapiens (human)
DOID:0110822
  • hereditary spastic paraplegia 77
  • Aliases:
    • SPG77
    • autosomal recessive spastic paraplegia 77
Homo sapiens (human)
DOID:0110772
  • hereditary spastic paraplegia 19
  • Aliases:
    • SPG19
    • autosomal dominant spastic paraplegia 19
    • autosomal dominant spastic paraplegia type 19
Homo sapiens (human)
DOID:0110793
  • hereditary spastic paraplegia 41
  • Aliases:
    • SPG41
    • autosomal dominant spastic paraplegia 41
    • autosomal dominant spastic paraplegia type 41
Homo sapiens (human)
DOID:0110780
  • hereditary spastic paraplegia 29
  • Aliases:
    • SPG29
    • autosomal dominant spastic paraplegia 29
Homo sapiens (human)
DOID:0110806
  • hereditary spastic paraplegia 54
  • Aliases:
    • SPG54
    • autosomal recessive spastic paraplegia 54
    • autosomal recessive spastic paraplegia type 54
Homo sapiens (human)
DOID:0060491
  • SPOAN syndrome
  • Aliases:
    • spastic paraplegia, optic atropy, and neuropathy
    • spastic paraplegia, optic atropy, and neuropathy syndrome
Homo sapiens (human)
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback

Click here to visit the beta site.

International Collaboration

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

Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.0.0

Last updated: August 19, 2024