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 8601 - 8625 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0111814
  • methylmalonic acidemia and homocysteinemia cblX type
  • Aliases:
    • combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX
    • mental retardation, X-linked 3
    • methylmalonic aciduria with homocystinuria, type cblX
Mus musculus (house mouse)
DOID:0111814
  • methylmalonic acidemia and homocysteinemia cblX type
  • Aliases:
    • combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX
    • mental retardation, X-linked 3
    • methylmalonic aciduria with homocystinuria, type cblX
Drosophila melanogaster (fruit fly)
DOID:0111808
  • linear skin defects with multiple congenital anomalies 1
  • Aliases:
    • MCOPS7
    • MIDAS syndrome
    • Microphthalmia with linear skin defect syndrome
    • microphthalmia-dermal aplasia-sclerocornea syndrome
    • syndromic microphthalmia 7
    • syndromic microphthalmia type 7
Mus musculus (house mouse)
DOID:8158
  • complement component 5 deficiency
  • Aliases:
    • C5 deficiency
Mus musculus (house mouse)
DOID:12556
  • acute kidney tubular necrosis
  • Aliases:
    • ATN - acute tubular necrosis
    • acute renal Failure with tubular necrosis
    • acute renal failure with lesion of tubular necrosis
    • acute tubular necrosis
    • acute tubule necrosis
Rattus norvegicus (Norway rat)
DOID:11111
  • hydronephrosis
Mus musculus (house mouse)
DOID:700
  • mitochondrial metabolism disease
Rattus norvegicus (Norway rat)
DOID:0111277
  • mitochondrial trifunctional protein deficiency
  • Aliases:
    • MTPD
    • TFP deficiency
    • TFPD
Mus musculus (house mouse)
DOID:0111277
  • mitochondrial trifunctional protein deficiency
  • Aliases:
    • MTPD
    • TFP deficiency
    • TFPD
Rattus norvegicus (Norway rat)
DOID:0070215
  • familial hyperinsulinemic hypoglycemia 4
  • Aliases:
    • HHF4
    • hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
    • hyperinsulinism due to SCHAD deficiency
    • hyperinsulinism due to glutamodehydrogenase deficiency
    • hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:0081337
  • congenital myopathy
Mus musculus (house mouse)
DOID:0111974
  • immunodeficiency 59
  • Aliases:
    • IMD59
    • granulocytopenia with immunoglobin abnormality
    • immunodeficiency 59 and hypoglycemia
Homo sapiens (human)
DOID:0110617
  • primary ciliary dyskinesia 5
  • Aliases:
    • CILD5
    • primary ciliary dyskinesia 5 without situs inversus
Homo sapiens (human)
DOID:0060793
  • hypomyelinating leukodystrophy 5
  • Aliases:
    • HLD5
    • hypomyelination-congenital cataract syndrome
Homo sapiens (human)
DOID:0050809
  • mucopolysaccharidosis IX
Homo sapiens (human)
DOID:0110196
  • Charcot-Marie-Tooth disease type 4G
  • Aliases:
    • CMT4G
    • Charcot-Marie-Tooth neuropathy type 4G
    • HMSNR
    • autosomal recessive Charcot-Marie-Tooth disease type 4G
    • hereditary motor and sensory neuropathy Russe type
Saccharomyces cerevisiae S288C
DOID:10923
  • sickle cell anemia
  • Aliases:
    • Hb SC disease
    • Hb-S/Hb-C disease
    • Hb-SS disease without crisis
    • Hemoglobin S disease without crisis
    • Sickle-cell/Hb-C disease without crisis
    • drepanocytosis
    • haemoglobin SC disease
    • hemoglobin SC disease
    • sickle cell anaemia
Saccharomyces cerevisiae S288C
DOID:2355
  • anemia
  • Aliases:
    • anaemia
Saccharomyces cerevisiae S288C
DOID:2861
  • congenital nonspherocytic hemolytic anemia
  • Aliases:
    • HNSHA
    • congenital nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anemia
Saccharomyces cerevisiae S288C
DOID:0060811
  • syndromic X-linked intellectual disability Turner type
  • Aliases:
    • Brooks-Wisniewski-Brown syndrome
    • MRXST
    • X-linked intellectual disability, Brooks type
    • mental retardation and macrocephaly syndrome
    • mental retardation, X-linked syndromic, Turner type
Homo sapiens (human)
DOID:0070403
  • hypomyelinating leukodystrophy 26
  • Aliases:
    • HLD26
Saccharomyces cerevisiae S288C
DOID:252
  • alcoholic psychosis
  • Aliases:
    • Alcoholic psychoses
Homo sapiens (human)
DOID:2537
  • inflammatory and toxic neuropathy
Homo sapiens (human)
DOID:0110739
  • neurodegeneration with brain iron accumulation 5
  • Aliases:
    • BPAN
    • Beta-Propeller Protein-Associated Neurodegeneration
    • NBIA5
    • SENDA
    • Static Encephalopathy Of Childhood With Neurodegeneration In Adulthood
Saccharomyces cerevisiae S288C
DOID:0090032
  • Silverman-Handmaker type dyssegmental dysplasia
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 v4.1.0

Last updated: December 9, 2024