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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 13626 - 13650 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0070246
  • X-linked Emery-Dreifuss muscular dystrophy 1
  • Aliases:
    • EDMD1
    • EMD1
    • Emery-Dreifuss muscular dystrophy 1, X-linked
    • humeroperoneal neuromuscular disease
    • muscular dystrophy, tardive, Dreifuss-Emery type, with contractures
    • scapuloperoneal syndrome, X-linked
Mus musculus (house mouse)
DOID:0070246
  • X-linked Emery-Dreifuss muscular dystrophy 1
  • Aliases:
    • EDMD1
    • EMD1
    • Emery-Dreifuss muscular dystrophy 1, X-linked
    • humeroperoneal neuromuscular disease
    • muscular dystrophy, tardive, Dreifuss-Emery type, with contractures
    • scapuloperoneal syndrome, X-linked
Homo sapiens (human)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Homo sapiens (human)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Drosophila melanogaster (fruit fly)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Caenorhabditis elegans
DOID:6683
  • X-linked Aarskog syndrome
  • Aliases:
    • Aarskog-Scott syndrome
    • Greig's syndrome
Homo sapiens (human)
DOID:0112063
  • X-Linked immunodeficiency 74
  • Aliases:
    • IMD74
    • TLR7 deficiency
    • X-linked immunodeficiency 74,COVID-19-related
    • respiratory insufficiency due to SARS-CoV-2 viral infection
Mus musculus (house mouse)
DOID:0112063
  • X-Linked immunodeficiency 74
  • Aliases:
    • IMD74
    • TLR7 deficiency
    • X-linked immunodeficiency 74,COVID-19-related
    • respiratory insufficiency due to SARS-CoV-2 viral infection
Homo sapiens (human)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Homo sapiens (human)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Mus musculus (house mouse)
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Caenorhabditis elegans
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Drosophila melanogaster (fruit fly)
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Homo sapiens (human)
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Mus musculus (house mouse)
DOID:10632
  • Wolfram syndrome
  • Aliases:
    • WFS
Homo sapiens (human)
DOID:10632
  • Wolfram syndrome
  • Aliases:
    • WFS
Drosophila melanogaster (fruit fly)
DOID:10632
  • Wolfram syndrome
  • Aliases:
    • WFS
Mus musculus (house mouse)
DOID:0110629
  • Wolfram syndrome 1
  • Aliases:
    • DIDMOAD
    • WFS1
    • diabetes mellitus AND insipidus with optic atrophy AND deafness
Homo sapiens (human)
DOID:0110629
  • Wolfram syndrome 1
  • Aliases:
    • DIDMOAD
    • WFS1
    • diabetes mellitus AND insipidus with optic atrophy AND deafness
Drosophila melanogaster (fruit fly)
DOID:0110629
  • Wolfram syndrome 1
  • Aliases:
    • DIDMOAD
    • WFS1
    • diabetes mellitus AND insipidus with optic atrophy AND deafness
Mus musculus (house mouse)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Homo sapiens (human)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Rattus norvegicus (Norway rat)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Caenorhabditis elegans
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Mus musculus (house mouse)
DOID:0050460
  • Wolf-Hirschhorn syndrome
  • Aliases:
    • 4p deletion syndrome
    • PITT SYNDROME
    • Pitt-Rogers-Danks Syndrome
    • chromosome 4p16.3 deletion syndrome
Homo sapiens (human)
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Last updated: December 9, 2024