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 5976 - 6000 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:4914
  • esophagus adenocarcinoma
  • Aliases:
    • Oesophageal adenocarcinoma
Homo sapiens (human)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Homo sapiens (human)
DOID:0111670
  • primary hyperoxaluria type 1
  • Aliases:
    • HP1
    • alanine-glyoxylate aminotransferase deficiency
    • glycolic aciduria
    • hepatic AGT deficiency
    • oxalosis I
    • peroxisomal alanine-glyoxylate aminotransferase deficiency
    • serine pyruvate aminotransferase deficiency
Homo sapiens (human)
DOID:8454
  • riboflavin deficiency
  • Aliases:
    • ariboflavinosis
    • vitamin B2 deficiency
Homo sapiens (human)
DOID:4985
  • extraosseous Ewings sarcoma-primitive neuroepithelial tumor
  • Aliases:
    • extraosseous Ewing's tumor
    • extraosseous Ewing's tumour
    • extraosseous Ewings sarcoma-primitive neuroepithelial tumour
Homo sapiens (human)
DOID:4232
  • extraosseous Ewing sarcoma
  • Aliases:
    • extraosseous Ewing's sarcoma
    • extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • extraskeletal Ewing sarcom
Homo sapiens (human)
DOID:0070152
  • hereditary sensory and autonomic neuropathy type 1A
  • Aliases:
    • HSAN1A
    • hereditary sensory and autonomic neuropathy type IA
Homo sapiens (human)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Homo sapiens (human)
DOID:0070162
  • hereditary sensory and autonomic neuropathy type 1
  • Aliases:
    • HSAN1
    • hereditary sensory and autonomic neuropathy type I
Homo sapiens (human)
DOID:2491
  • sensory peripheral neuropathy
  • Aliases:
    • peripheral Sensory Neuropathy
    • sensory neuropathy
Homo sapiens (human)
DOID:0111350
  • Laurin-Sandrow syndrome
  • Aliases:
    • MIPduplication of fibuland ulna with absence of tibia and radius
    • Sandrow syndrome
    • TMIP
    • miccor hands and feet with nasal defects
    • mirror hands and feets-nasal defects syndrome
    • mirror-image polydactyly
    • tetramelic mirror-image polydactyly
Homo sapiens (human)
DOID:0070313
  • thiamine deficiency disease
Homo sapiens (human)
DOID:13725
  • beriberi
Homo sapiens (human)
DOID:2977
  • primary hyperoxaluria
Homo sapiens (human)
DOID:0110946
  • autosomal recessive osteopetrosis 7
  • Aliases:
    • OPTB7
    • autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • autosomal recessive osteopetrosis type 7
    • osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • osteopetrosis-hypogammaglobulinemia syndrome
Homo sapiens (human)
DOID:4254
  • osteosclerosis
Homo sapiens (human)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Homo sapiens (human)
DOID:10575
  • calcium metabolism disease
Homo sapiens (human)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Homo sapiens (human)
DOID:0110657
  • congenital myasthenic syndrome 8
  • Aliases:
    • CMS8
    • congenital myasthenic syndrome 8 with pre- and postsynaptic defects
    • congenital myasthenic syndrome due to agrin deficiency
Homo sapiens (human)
DOID:0110668
  • congenital myasthenic syndrome 10
  • Aliases:
    • CMS10
    • LGM
    • congenital muscular dystrophy merosin-positive
    • familial limb-girdle myasthenia
Homo sapiens (human)
DOID:0111375
  • fetal akinesia deformation sequence syndrome
  • Aliases:
    • FADS
    • Pena-Shokeir syndrome type 1
    • arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome
    • fetal akinesia sequence
    • foetal akinesia deformation sequence syndrome
    • foetal akinesia sequence
Homo sapiens (human)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Homo sapiens (human)
DOID:681
  • progressive bulbar palsy
Homo sapiens (human)
DOID:9840
  • esotropia
  • Aliases:
    • Convergence in manifest squint
    • Internal Strabismus
    • crossed eyes
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