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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 12201 - 12225 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0070467
  • carpal tunnel syndrome 2
  • Aliases:
    • CTS2
Homo sapiens (human)
DOID:12721
  • multiple epiphyseal dysplasia
  • Aliases:
    • polyepiphyseal dysplasia
Homo sapiens (human)
DOID:0070303
  • multiple epiphyseal dysplasia 1
  • Aliases:
    • EDM1
    • MED1
    • multiple epiphyseal dysplasia COMP-related
    • polyepiphyseal dysplasia type 1
Homo sapiens (human)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Homo sapiens (human)
DOID:0060576
  • 3MC syndrome 2
Homo sapiens (human)
DOID:0060577
  • 3MC syndrome 3
Homo sapiens (human)
DOID:0070304
  • multiple epiphyseal dysplasia 3
  • Aliases:
    • EDM3
    • multiple epiphyseal dysplasia 3 with or without myopathy
Homo sapiens (human)
DOID:0070298
  • multiple epiphyseal dysplasia 2
  • Aliases:
    • EDM2
Homo sapiens (human)
DOID:0070301
  • multiple epiphyseal dysplasia 6
  • Aliases:
    • EDM6
Homo sapiens (human)
DOID:0110856
  • posterior polymorphous corneal dystrophy 2
  • Aliases:
    • Ppcd2
Homo sapiens (human)
DOID:0111347
  • epidermolysis bullosa with congenital localized absence of skin and deformity of nails
  • Aliases:
    • EBD, Bart type
    • epidermolysis bullosa dystrophica, Bart type
Homo sapiens (human)
DOID:0080224
  • autosomal dominant dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:0080988
  • pretibial dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:0111345
  • transient bullous dermolysis of the newborn
  • Aliases:
    • DEB, bullous dermolysis of the newborn
    • DEB-BDN
Homo sapiens (human)
DOID:0080086
  • nonsyndromic congenital nail disorder 8
  • Aliases:
    • isolated toenail dystrophy
Homo sapiens (human)
DOID:4959
  • epidermolysis bullosa dystrophica
  • Aliases:
    • Dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:0060642
  • recessive dystrophic epidermolysis bullosa
  • Aliases:
    • RDEB, Hallopeau-Siemens type
    • autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
    • autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type
Homo sapiens (human)
DOID:0090050
  • dystonia 27
Homo sapiens (human)
DOID:2033
  • communication disorder
Homo sapiens (human)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Homo sapiens (human)
DOID:0050557
  • congenital muscular dystrophy
Homo sapiens (human)
DOID:0080726
  • Ehlers-Danlos syndrome classic type 2
Homo sapiens (human)
DOID:14720
  • Ehlers-Danlos syndrome classic type 1
  • Aliases:
    • Ehlers-Danlos syndrome, type 1
    • type I Ehlers-Danlos syndrome
Homo sapiens (human)
DOID:0111740
  • X-linked deafness 6
  • Aliases:
    • DFNX6
Homo sapiens (human)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Homo sapiens (human)
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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

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Last updated: December 9, 2024