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 1876 - 1900 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0112045
  • non-syndromic X-linked intellectual disability 93
  • Aliases:
    • MRX93
    • X-linked mental retardation 93
    • X-linked mental retardation with macrocephaly
Homo sapiens (human)
DOID:0112040
  • non-syndromic X-linked intellectual disability 100
  • Aliases:
    • MRX100
    • X-linked mental retardation 100
Homo sapiens (human)
DOID:0112038
  • non-syndromic X-linked intellectual disability 1
  • Aliases:
    • MRX1
    • MRX18
    • MRX78
    • X-linked mental retardation 1
    • X-linked mental retardation 1/78
    • X-linked mental retardation 18
    • X-linked mental retardation 78
Homo sapiens (human)
DOID:0112035
  • non-syndromic X-linked intellectual disability 96
  • Aliases:
    • MRX96
    • X-linked mental retardation 96
Homo sapiens (human)
DOID:0112034
  • non-syndromic X-linked intellectual disability 9
  • Aliases:
    • MRX44
    • MRX9
    • X-linked mental retardation 44
    • X-linked mental retardation 9
Homo sapiens (human)
DOID:0112029
  • non-syndromic X-linked intellectual disability 50
  • Aliases:
    • MRX50
    • X-linked intellectual developmental disorder 50
    • X-linked mental retardation 50
    • XLID50
Homo sapiens (human)
DOID:0112026
  • non-syndromic X-linked intellectual disability 99
  • Aliases:
    • MRX99
    • X-linked mental retardation 99
Homo sapiens (human)
DOID:0112025
  • female-restricted syndromic X-linked intellectual disability 99
  • Aliases:
    • MRXS99F
    • X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
    • female-restricted syndromic X-linked mental retardation 99
Homo sapiens (human)
DOID:0112024
  • non-syndromic X-linked intellectual disability 58
  • Aliases:
    • MRX58
    • X-linked mental retardation 58
Homo sapiens (human)
DOID:0112022
  • non-syndromic X-linked intellectual disability 21
  • Aliases:
    • MRX21
    • MRX34
    • X-linked mental retardation 21
    • X-linked mental retardation 21/34
    • X-linked mental retardation 34
Homo sapiens (human)
DOID:0112021
  • non-syndromic X-linked intellectual disability ARX-related
  • Aliases:
    • ARX-related intellectual disability
    • MRXARX
    • X-linked mental retardation 29
    • X-linked mental retardation 29 and others
    • X-linked mental retardation 32
    • X-linked mental retardation 33
    • X-linked mental retardation 38
    • X-linked mental retardation 43
    • X-linked mental retardation 52
    • X-linked mental retardation 54
    • X-linked mental retardation 76
    • X-linked mental retardation 87
    • X-linked mental retardation with or without seizures ARX-related
Homo sapiens (human)
DOID:0112019
  • non-syndromic X-linked intellectual disability 19
  • Aliases:
    • MRX19
    • X-linked mental retardation 19
Homo sapiens (human)
DOID:0112018
  • non-syndromic X-linked intellectual disability 104
  • Aliases:
    • MRX104
    • X-linked mental retardation 104
Homo sapiens (human)
DOID:0112012
  • X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques
  • Aliases:
    • OLMSX
    • X-linked Olmsted syndrome
Homo sapiens (human)
DOID:0112010
  • pituitary adenoma 3
  • Aliases:
    • PITA3
    • pituitary adenoma 3, multiple types
Homo sapiens (human)
DOID:0112008
  • pituitary adenoma 5
  • Aliases:
    • PITA5
    • pituitary adenoma 5, multiple types
Homo sapiens (human)
DOID:0112007
  • growth hormone secreting pituitary adenoma 2
  • Aliases:
    • GH-secreting pituitary adenoma 2
    • PITA2
    • X-linked acromegaly
    • acromegaly due to pituitary adenoma 2
Homo sapiens (human)
DOID:0112006
  • immunodeficiency 69
  • Aliases:
    • IMD69
Homo sapiens (human)
DOID:0112004
  • immunodeficiency 71
  • Aliases:
    • IMD71
    • PLTEID
    • immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia
    • platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
Homo sapiens (human)
DOID:0112002
  • immunodeficiency 47
  • Aliases:
    • CDG IIs
    • CDG2S
    • CDGIIs
    • IMD47
    • congenital disorder of glycosylation type IIs
    • immunodeficiency and hepatopathy with or without neurologic features
Homo sapiens (human)
DOID:0112001
  • immunodeficiency 50
  • Aliases:
    • CID due to Moesin deficiency
    • IMD50
    • MSN-related combined immunodeficiency
    • X-linked Moesin-associated immunodeficiency
    • combined immunodeficiency due to Moesin deficiency
    • immunodeficiency 50 X linked recessive
Homo sapiens (human)
DOID:0112000
  • immunodeficiency 34
  • Aliases:
    • AMCBX2
    • IMD34
    • X-linked MSMD due to CYBB deficiency
    • X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
    • familial atypical mycobacteriosis X-linked 2
    • immunodeficiency 34, mycobacteriosis, X-linked
Homo sapiens (human)
DOID:0111999
  • immunodeficiency 61
  • Aliases:
    • IMD61
Homo sapiens (human)
DOID:0111998
  • immunodeficiency 66
  • Aliases:
    • IMD66
Homo sapiens (human)
DOID:0111997
  • immunodeficiency 63
  • Aliases:
    • IL2RB deficiency
    • IMD63
    • immunodeficiency 63 with lymphoproliferation and autoimmunity
Homo sapiens (human)

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Last updated: December 9, 2024