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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2801 - 2825 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0110551
  • autosomal dominant nonsyndromic deafness 21
  • Aliases:
    • DFNA21
    • autosomal dominant deafness 21
Homo sapiens (human)
DOID:0110481
  • autosomal recessive nonsyndromic deafness 23
  • Aliases:
    • DFNB23
    • autosomal recessive deafness 23
Homo sapiens (human)
DOID:0110492
  • autosomal recessive nonsyndromic deafness 33
  • Aliases:
    • DFNB33
    • autosomal recessive deafness 33
Homo sapiens (human)
DOID:0110501
  • autosomal recessive nonsyndromic deafness 44
  • Aliases:
    • DFNB44
    • autosomal recessive deafness 44
Homo sapiens (human)
DOID:0110534
  • autosomal recessive nonsyndromic deafness 89
  • Aliases:
    • DFNB89
    • autosomal recessive deafness 89
Homo sapiens (human)
DOID:0110491
  • autosomal recessive nonsyndromic deafness 32
  • Aliases:
    • DFNB32
    • HIIMS
    • autosomal recessive deafness 105
    • autosomal recessive deafness 32
    • hearing impairment infertile male syndrome
Homo sapiens (human)
DOID:0110550
  • autosomal dominant nonsyndromic deafness 20
  • Aliases:
    • DFNA20
    • DFNA26
    • autosomal dominant deafness 20
Homo sapiens (human)
DOID:0110507
  • autosomal recessive nonsyndromic deafness 5
  • Aliases:
    • DFNB5
    • autosomal recessive deafness 5
Homo sapiens (human)
DOID:0110476
  • autosomal recessive nonsyndromic deafness 1B
  • Aliases:
    • DFNB1B
    • autosomal recessive deafness 1B
Homo sapiens (human)
DOID:0110547
  • autosomal dominant nonsyndromic deafness 16
  • Aliases:
    • DFNA16
    • autosomal dominant deafness 16
Homo sapiens (human)
DOID:0110528
  • autosomal recessive nonsyndromic deafness 83
  • Aliases:
    • DFNB83
    • autosomal recessive deafness 83
Homo sapiens (human)
DOID:0110577
  • autosomal dominant nonsyndromic deafness 51
  • Aliases:
    • DFNA51
    • autosomal dominant deafness 51
    • chromosome 9q21.11 duplication syndrome
Homo sapiens (human)
DOID:0110515
  • autosomal recessive nonsyndromic deafness 63
  • Aliases:
    • DFNB63
    • autosomal recessive deafness 63
Homo sapiens (human)
DOID:0110463
  • autosomal recessive nonsyndromic deafness 102
  • Aliases:
    • DFNB102
    • autosomal recessive deafness 102
Homo sapiens (human)
DOID:0110477
  • autosomal recessive nonsyndromic deafness 2
  • Aliases:
    • DFNB2
    • autosomal recessive deafness 2
Homo sapiens (human)
DOID:0110572
  • autosomal dominant nonsyndromic deafness 49
  • Aliases:
    • DFNA49
    • autosomal dominant deafness 49
Homo sapiens (human)
DOID:0110543
  • autosomal dominant nonsyndromic deafness 11
  • Aliases:
    • DFNA11
    • autosomal dominant deafness 11
Homo sapiens (human)
DOID:0110576
  • autosomal dominant nonsyndromic deafness 50
  • Aliases:
    • DFNA50
    • autosomal dominant deafness 50
Homo sapiens (human)
DOID:0110487
  • autosomal recessive nonsyndromic deafness 29
  • Aliases:
    • DFNB29
    • autosomal recessive deafness 29
Homo sapiens (human)
DOID:0110546
  • autosomal dominant nonsyndromic deafness 15
  • Aliases:
    • DFNA15
    • autosomal dominant deafness 15
Homo sapiens (human)
DOID:0110552
  • autosomal dominant nonsyndromic deafness 22
  • Aliases:
    • DFNA22
    • autosomal dominant deafness 22
Homo sapiens (human)
DOID:0110578
  • autosomal dominant nonsyndromic deafness 52
  • Aliases:
    • DFNA52
    • autosomal dominant deafness 52
Homo sapiens (human)
DOID:0110545
  • autosomal dominant nonsyndromic deafness 13
  • Aliases:
    • DFNA13
    • autosomal dominant deafness 13
Homo sapiens (human)
DOID:0110549
  • autosomal dominant nonsyndromic deafness 18
  • Aliases:
    • DFNA18
    • autosomal dominant deafness 18
Homo sapiens (human)
DOID:10017
  • multiple endocrine neoplasia type 1
  • Aliases:
    • MEN type I
    • Wermer syndrome
    • Wermer's syndrome
Homo sapiens (human)
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Last updated: August 19, 2024