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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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 8026 - 8050 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0110555
  • autosomal dominant nonsyndromic deafness 25
  • Aliases:
    • DFNA25
    • autosomal dominant deafness 25
Homo sapiens (human)
DOID:9784
  • trichinosis
  • Aliases:
    • Trichinella spiralis infection
Homo sapiens (human)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Mus musculus (house mouse)
DOID:0050947
  • hereditary hypophosphatemic rickets with hypercalciuria
Rattus norvegicus (Norway rat)
DOID:0111941
  • immunodeficiency 20
  • Aliases:
    • CD16 deficiency
    • IMD20
    • autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity
    • autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
Mus musculus (house mouse)
DOID:1587
  • thrombocytopenia due to platelet alloimmunization
  • Aliases:
    • Auto-immune thrombocytopenia
    • Immune thrombocytopenia
    • Thrombocytopenia Due to Immune Destruction
Mus musculus (house mouse)
DOID:0060462
  • Desbuquois dysplasia
  • Aliases:
    • Desbuquois syndrome
    • micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
Rattus norvegicus (Norway rat)
DOID:0070302
  • multiple epiphyseal dysplasia 7
  • Aliases:
    • EDM7
Rattus norvegicus (Norway rat)
DOID:12215
  • oligohydramnios
  • Aliases:
    • Oligohydramnios - delivered
    • antepartum oligohydramnios
    • delivered oligohydramnios
Rattus norvegicus (Norway rat)
DOID:0060230
  • basal ganglia calcification
  • Aliases:
    • Fahr disease
Rattus norvegicus (Norway rat)
DOID:3507
  • dermatofibrosarcoma protuberans
Rattus norvegicus (Norway rat)
DOID:4586
  • familial meningioma
Rattus norvegicus (Norway rat)
DOID:13619
  • extrahepatic cholestasis
  • Aliases:
    • extrahepatic biliary Stasis
    • extrahepatic obstructive biliary disease
Rattus norvegicus (Norway rat)
DOID:0080109
  • infantile myofibromatosis
  • Aliases:
    • lipofibromatosis
Rattus norvegicus (Norway rat)
DOID:8946
  • severe nonproliferative diabetic retinopathy
  • Aliases:
    • High risk non proliferative diabetic retinopathy
    • Severe NPDR
Rattus norvegicus (Norway rat)
DOID:2226
  • myeloproliferative neoplasm
  • Aliases:
    • CMPD
    • CMPD, U
    • chronic myeloproliferative disease
Rattus norvegicus (Norway rat)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Rattus norvegicus (Norway rat)
DOID:0090092
  • hypogonadotropic hypogonadism 3 with or without anosmia
Mus musculus (house mouse)
DOID:0110289
  • autosomal recessive limb-girdle muscular dystrophy type 2Y
  • Aliases:
    • LGMD2Y
    • autosomal recessive muscular dystrophy due to LAP1B deficiency
    • autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency
    • muscular dystrophy with progressive weakness, distal contractures and rigid spine
    • muscular dystrophy, limb-girdle, type 2Y
Rattus norvegicus (Norway rat)
DOID:6419
  • tetralogy of Fallot
  • Aliases:
    • Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle
Rattus norvegicus (Norway rat)
DOID:0111933
  • phosphoglycerate kinase 1 deficiency
  • Aliases:
    • GSD due to phosphoglycerate kinase 1 deficiency
    • PGK1 deficiency
    • glycogen storage disease due to phosphoglycerate kinase 1 deficiency
    • glycogenosis due to phosphoglycerate kinase 1 deficiency
Rattus norvegicus (Norway rat)
DOID:2913
  • acute pancreatitis
Rattus norvegicus (Norway rat)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Rattus norvegicus (Norway rat)
DOID:0060186
  • chemical colitis
Rattus norvegicus (Norway rat)
DOID:1926
  • Gaucher's disease
  • Aliases:
    • Gaucher disease
    • acid beta-glucosidase deficiency
    • glocucerebrosidase deficiency
    • glucosylceramide beta-glucosidase deficiency
    • kerasin thesaurismosis
Rattus norvegicus (Norway rat)
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 v4.1.0

Last updated: December 9, 2024