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 5276 - 5300 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0050669
  • spastic cerebral palsy
Homo sapiens (human)
DOID:9274
  • hyperlysinemia
Homo sapiens (human)
DOID:0111254
  • glutaric acidemia I
  • Aliases:
    • GA1
    • glutaric academia type 1
    • glutaric aciduria 1
    • glutaric aciduria type I
    • glutaryl-coA dehydrogenase deficiency
    • glutaryl-coenzyme A dehydrogenase deficiency
Homo sapiens (human)
DOID:28
  • endocrine system disease
Homo sapiens (human)
DOID:12700
  • hyperprolactinemia
  • Aliases:
    • Chiari-Frommel syndrome
    • Pregnancy-related A-G syndrome
    • hyperprolactinaemia
Homo sapiens (human)
DOID:9212
  • pityriasis rubra pilaris
  • Aliases:
    • Devergie's disease
Homo sapiens (human)
DOID:12883
  • hypochondriasis
  • Aliases:
    • Hypochondria
    • Hypochondriacal disorder
    • hypochondriacal neurosis
Homo sapiens (human)
DOID:0112223
  • developmental and epileptic encephalopathy 89
  • Aliases:
    • DEE89
    • early infantile epileptic encephalopathy 89
Homo sapiens (human)
DOID:439
  • neuromuscular junction disease
Homo sapiens (human)
DOID:1827
  • idiopathic generalized epilepsy
  • Aliases:
    • Generalised epilepsy
Homo sapiens (human)
DOID:0111382
  • ischiocoxopodopatellar syndrome
  • Aliases:
    • SPS
    • Scott-Taor syndrome
    • congenital coxa vara, patella aplasia and tarsal synostosis
    • coxo-podo-patellar syndrome
    • coxopodipatellar syndrome
    • ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension
    • ischiopatellar dysplasia
    • patella aplasia, coxa vara, and tarsal synostosis
    • small patella syndrome
Homo sapiens (human)
DOID:4440
  • seminoma
  • Aliases:
    • Seminoma, Pure
Rattus norvegicus (Norway rat)
DOID:0080178
  • mucositis
Rattus norvegicus (Norway rat)
DOID:3571
  • liver cancer
  • Aliases:
    • Ca liver - primary
    • Resectable malignant neoplasm of Liver
    • hepatic cancer
    • hepatic neoplasm
    • malignant hepato-biliary neoplasm
    • malignant neoplasm of liver
    • malignant neoplasm of liver, not specified as primary or secondary
    • malignant neoplasm of liver, primary
    • malignant tumor of liver
    • neoplasm of liver
    • non-resectable primary hepatic malignant neoplasm
    • primary liver cancer
    • primary malignant neoplasm of liver
    • resectable malignant neoplasm of the liver
Rattus norvegicus (Norway rat)
DOID:0081385
  • ataxia-telangiectasia-like disorder-2
  • Aliases:
    • PCNA-related progressive neurodegenerative photosensitivity syndrome
Rattus norvegicus (Norway rat)
DOID:9427
  • hypertensive encephalopathy
Rattus norvegicus (Norway rat)
DOID:0090129
  • carnitine palmitoyltransferase I deficiency
  • Aliases:
    • CPT I deficiency
    • CPT1A deficiency
    • L-CPT1 deficiency
    • carnitine palmitoyl transferase 1A deficiency
    • carnitine palmitoyl transferase IA deficiency
    • hepatic CPT deficiency type I
    • hepatic carnitine palmitoyl transferase 1 deficiency
    • hepatic carnitine palmitoyl transferase I deficiency
Rattus norvegicus (Norway rat)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Homo sapiens (human)
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Homo sapiens (human)
DOID:14264
  • benign neonatal seizures
  • Aliases:
    • benign familial neonatal seizures
    • benign neonatal convulsions
Homo sapiens (human)
DOID:14777
  • benign familial neonatal epilepsy
  • Aliases:
    • familial neonatal seizures
Homo sapiens (human)
DOID:0060169
  • benign familial infantile epilepsy
  • Aliases:
    • BFIC
    • BFIE
    • benign familial infantile convulsion
    • benign familial infantile seizures
Homo sapiens (human)
DOID:0070262
  • congenital disorder of glycosylation type IIj
  • Aliases:
    • CDG IIj
    • CDG syndrome type IIj
    • CDG2J
    • CDGIIdj
    • COG4-CDG
    • Carbohydrate deficient glycoprotein syndrome type IIj
    • Congenital disorder of glycosylation type 2j
Homo sapiens (human)
DOID:0111673
  • Saul-Wilson syndrome
  • Aliases:
    • SWILS
    • microcephalic osteodysplastic dysplasia, Saul-Wilson type
Homo sapiens (human)
DOID:0110414
  • retinitis pigmentosa 3
  • Aliases:
    • RP3
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