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) 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 6676 - 6700 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0110918
  • hereditary spherocytosis type 3
  • Aliases:
    • HS3
    • SPH3
    • hereditary spherocytosis 3
Mus musculus (house mouse)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Homo sapiens (human)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Rattus norvegicus (Norway rat)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Mus musculus (house mouse)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Caenorhabditis elegans
DOID:0110920
  • hereditary spherocytosis type 5
  • Aliases:
    • HS5
    • SPH5
    • hereditary spherocytosis 5
Homo sapiens (human)
DOID:0110922
  • familial hemophagocytic lymphohistiocytosis 2
  • Aliases:
    • FHL2
    • HLH2
    • HPLH2
Mus musculus (house mouse)
DOID:0110922
  • familial hemophagocytic lymphohistiocytosis 2
  • Aliases:
    • FHL2
    • HLH2
    • HPLH2
Homo sapiens (human)
DOID:0110923
  • familial hemophagocytic lymphohistiocytosis 3
  • Aliases:
    • FHL3
    • HLH3
    • HPLH3
Homo sapiens (human)
DOID:0110925
  • familial hemophagocytic lymphohistiocytosis 5
  • Aliases:
    • FHL5
    • HLH5
    • HPLH5
Homo sapiens (human)
DOID:0110927
  • nemaline myopathy 3
  • Aliases:
    • NEM3
    • congenital myopathy 2A
    • nemaline myopathy 3, autosomal dominant or recessive
Mus musculus (house mouse)
DOID:0110927
  • nemaline myopathy 3
  • Aliases:
    • NEM3
    • congenital myopathy 2A
    • nemaline myopathy 3, autosomal dominant or recessive
Homo sapiens (human)
DOID:0110927
  • nemaline myopathy 3
  • Aliases:
    • NEM3
    • congenital myopathy 2A
    • nemaline myopathy 3, autosomal dominant or recessive
Rattus norvegicus (Norway rat)
DOID:0110928
  • nemaline myopathy 2
  • Aliases:
    • NEM2
    • congenital myopathy 2
    • nemaline myopathy 2, autosomal recessive
Homo sapiens (human)
DOID:0110928
  • nemaline myopathy 2
  • Aliases:
    • NEM2
    • congenital myopathy 2
    • nemaline myopathy 2, autosomal recessive
Mus musculus (house mouse)
DOID:0110933
  • nemaline myopathy 11
  • Aliases:
    • NEM11
    • nemaline myopathy 11, autosomal recessive
Mus musculus (house mouse)
DOID:0110933
  • nemaline myopathy 11
  • Aliases:
    • NEM11
    • nemaline myopathy 11, autosomal recessive
Homo sapiens (human)
DOID:0110934
  • nemaline myopathy 7
  • Aliases:
    • NEM7
    • nemaline myopathy 7, autosomal recessive
Homo sapiens (human)
DOID:0110934
  • nemaline myopathy 7
  • Aliases:
    • NEM7
    • nemaline myopathy 7, autosomal recessive
Mus musculus (house mouse)
DOID:0110934
  • nemaline myopathy 7
  • Aliases:
    • NEM7
    • nemaline myopathy 7, autosomal recessive
Saccharomyces cerevisiae S288C
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Homo sapiens (human)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Mus musculus (house mouse)
DOID:0110939
  • autosomal recessive osteopetrosis 5
  • Aliases:
    • OPTB5
    • infantile malignant osteopetrosis 3
Mus musculus (house mouse)
DOID:0110939
  • autosomal recessive osteopetrosis 5
  • Aliases:
    • OPTB5
    • infantile malignant osteopetrosis 3
Homo sapiens (human)
DOID:0110942
  • autosomal recessive osteopetrosis 1
  • Aliases:
    • OPTB1
    • autosomal recessive Albers-Schonberg disease
    • infantile malignant osteopetrosis 1
Caenorhabditis elegans
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback
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