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 726 - 750 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0070033
  • autosomal dominant intellectual developmental disorder 3
  • Aliases:
    • MRD3
    • autosomal dominant mental retardation 3
    • autosomal dominant non-syndromic intellectual disability 3
Homo sapiens (human)
DOID:0070035
  • autosomal dominant intellectual developmental disorder 5
  • Aliases:
    • MRD5
    • autosomal dominant mental retardation 5
    • autosomal dominant non-syndromic intellectual disability 5
Homo sapiens (human)
DOID:0070036
  • autosomal dominant intellectual developmental disorder 6
  • Aliases:
    • MRD6
    • autosomal dominant mental retardation 6
    • autosomal dominant non-syndromic intellectual disability 6
Homo sapiens (human)
DOID:0070037
  • autosomal dominant intellectual developmental disorder 7
  • Aliases:
    • DYRK1A syndrome
    • MRD7
    • autosomal dominant mental retardation 7
    • autosomal dominant non-syndromic intellectual disability 7
Homo sapiens (human)
DOID:0070038
  • autosomal dominant intellectual developmental disorder 8
  • Aliases:
    • MRD8
    • autosomal dominant mental retardation 8
    • autosomal dominant non-syndromic intellectual disability 8
Homo sapiens (human)
DOID:0070040
  • autosomal dominant intellectual developmental disorder 10
  • Aliases:
    • MRD10
    • autosomal dominant mental retardation 10
    • autosomal dominant non-syndromic intellectual disability 10
Homo sapiens (human)
DOID:0070041
  • autosomal dominant intellectual developmental disorder 11
  • Aliases:
    • MRD11
    • autosomal dominant mental retardation 11
    • autosomal dominant non-syndromic intellectual disability 11
Homo sapiens (human)
DOID:0070042
  • Coffin-Siris syndrome 1
  • Aliases:
    • CSS1
    • MRD12
    • autosomal dominant mental retardation 12
    • fifth digit syndrome
Homo sapiens (human)
DOID:0070043
  • autosomal dominant intellectual developmental disorder 13
  • Aliases:
    • MRD13
    • autosomal dominant mental retardation 13
    • autosomal dominant non-syndromic intellectual disability 13
    • mental retardation, autosomal dominant 13, with neuronal migration defects
Homo sapiens (human)
DOID:0070044
  • Coffin-Siris syndrome 2
  • Aliases:
    • CSS2
    • MRD14
    • autosomal dominant mental retardation 14
Homo sapiens (human)
DOID:0070045
  • Coffin-Siris syndrome 3
  • Aliases:
    • CSS3
    • MRD15
    • autosomal dominant mental retardation 15
Homo sapiens (human)
DOID:0070046
  • Coffin-Siris syndrome 4
  • Aliases:
    • CSS4
    • MRD16
    • autosomal dominant mental retardation 16
Homo sapiens (human)
DOID:0070047
  • Schuurs-Hoeijmakers Syndrome
  • Aliases:
    • MRD17
    • SHMS
    • autosomal dominant mental retardation 17
Homo sapiens (human)
DOID:0070048
  • GAND syndrome
  • Aliases:
    • MRD18
    • autosomal dominant intellectual developmental disorder 18
    • autosomal dominant mental retardation 18
    • autosomal dominant non-syndromic intellectual disability 18
Homo sapiens (human)
DOID:0070049
  • autosomal dominant intellectual developmental disorder 19
  • Aliases:
    • MRD19
    • autosomal dominant mental retardation 19
    • autosomal dominant non-syndromic intellectual disability 19
Homo sapiens (human)
DOID:0070050
  • neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language
  • Aliases:
    • MRD20
    • autosomal dominant mental retardation 20
    • mental retardation, autosomal dominant 20
Homo sapiens (human)
DOID:0070051
  • autosomal dominant intellectual developmental disorder 21
  • Aliases:
    • MRD21
    • autosomal dominant mental retardation 21
    • autosomal dominant non-syndromic intellectual disability 21
Homo sapiens (human)
DOID:0070053
  • autosomal dominant intellectual developmental disorder 23
  • Aliases:
    • MRD23
    • autosomal dominant mental retardation 23
    • autosomal dominant non-syndromic intellectual disability 23
Homo sapiens (human)
DOID:0070054
  • Vulto-van Silfout-de Vries syndrome
  • Aliases:
    • IDDISBAS
    • MRD24
    • VSVS
    • autosomal dominant mental retardation 24
    • autosomal dominant non-syndromic intellectual disability 24
    • intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures
Homo sapiens (human)
DOID:0070055
  • Xia-Gibbs Syndrome
  • Aliases:
    • MRD25
    • autosomal dominant mental retardation 25
Homo sapiens (human)
DOID:0070056
  • autosomal dominant intellectual developmental disorder 26
  • Aliases:
    • MRD26
    • autosomal dominant mental retardation 26
    • autosomal dominant non-syndromic intellectual disability 26
Homo sapiens (human)
DOID:0070058
  • Helsmoortel-Van Der Aa Syndrome
  • Aliases:
    • HVDAS
    • MRD28
    • autosomal dominant mental retardation 28
Homo sapiens (human)
DOID:0070059
  • autosomal dominant intellectual developmental disorder 29
  • Aliases:
    • MRD29
    • autosomal dominant mental retardation 29
    • autosomal dominant non-syndromic intellectual disability 29
Homo sapiens (human)
DOID:0070062
  • Arboleda-Tham syndrome
  • Aliases:
    • ARTHS
    • MRD32
    • autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
    • autosomal dominant mental retardation 32
    • autosomal dominant non-syndromic intellectual disability 32
Homo sapiens (human)
DOID:0070063
  • autosomal dominant intellectual developmental disorder 33
  • Aliases:
    • MRD33
    • autosomal dominant mental retardation 33
    • autosomal dominant non-syndromic intellectual disability 33
Homo sapiens (human)

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Last updated: December 9, 2024