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 3101 - 3125 of 4621 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0110565
  • autosomal dominant nonsyndromic deafness 3B
  • Aliases:
    • DFNA3B
    • autosomal dominant deafness 3B
Homo sapiens (human)
DOID:0110564
  • autosomal dominant nonsyndromic deafness 3A
  • Aliases:
    • DFNA3A
    • autosomal dominant deafness 3A
Homo sapiens (human)
DOID:0110563
  • autosomal dominant nonsyndromic deafness 36
  • Aliases:
    • DFNA36
    • autosomal dominant deafness 36
Homo sapiens (human)
DOID:0110562
  • autosomal dominant nonsyndromic deafness 33
  • Aliases:
    • DFNA33
    • autosomal dominant deafness 33
Homo sapiens (human)
DOID:0110561
  • autosomal dominant nonsyndromic deafness 31
  • Aliases:
    • DFNA31
    • autosomal dominant deafness 31
Homo sapiens (human)
DOID:0110560
  • autosomal dominant nonsyndromic deafness 30
  • Aliases:
    • DFNA30
    • autosomal dominant deafness 30
Homo sapiens (human)
DOID:0110559
  • autosomal dominant nonsyndromic deafness 2B
  • Aliases:
    • DFNA2B
    • autosomal dominant deafness 2B
Homo sapiens (human)
DOID:0110558
  • autosomal dominant nonsyndromic deafness 2A
  • Aliases:
    • DFNA2A
    • autosomal dominant deafness 2A
Homo sapiens (human)
DOID:0110557
  • autosomal dominant nonsyndromic deafness 28
  • Aliases:
    • DFNA28
    • autosomal dominant deafness 28
Homo sapiens (human)
DOID:0110556
  • autosomal dominant nonsyndromic deafness 27
  • Aliases:
    • DFNA27
    • autosomal dominant deafness 27
Homo sapiens (human)
DOID:0110555
  • autosomal dominant nonsyndromic deafness 25
  • Aliases:
    • DFNA25
    • autosomal dominant deafness 25
Homo sapiens (human)
DOID:0110554
  • autosomal dominant nonsyndromic deafness 24
  • Aliases:
    • DFNA24
    • autosomal dominant deafness 24
Homo sapiens (human)
DOID:0110553
  • autosomal dominant nonsyndromic deafness 23
  • Aliases:
    • DFNA23
    • autosomal dominant deafness 23
Homo sapiens (human)
DOID:0110552
  • autosomal dominant nonsyndromic deafness 22
  • Aliases:
    • DFNA22
    • autosomal dominant deafness 22
Homo sapiens (human)
DOID:0110551
  • autosomal dominant nonsyndromic deafness 21
  • Aliases:
    • DFNA21
    • autosomal dominant deafness 21
Homo sapiens (human)
DOID:0110550
  • autosomal dominant nonsyndromic deafness 20
  • Aliases:
    • DFNA20
    • DFNA26
    • autosomal dominant deafness 20
Homo sapiens (human)
DOID:0110549
  • autosomal dominant nonsyndromic deafness 18
  • Aliases:
    • DFNA18
    • autosomal dominant deafness 18
Homo sapiens (human)
DOID:0110548
  • autosomal dominant nonsyndromic deafness 17
  • Aliases:
    • DFNA17
    • autosomal dominant deafness 17
Homo sapiens (human)
DOID:0110547
  • autosomal dominant nonsyndromic deafness 16
  • Aliases:
    • DFNA16
    • autosomal dominant deafness 16
Homo sapiens (human)
DOID:0110546
  • autosomal dominant nonsyndromic deafness 15
  • Aliases:
    • DFNA15
    • autosomal dominant deafness 15
Homo sapiens (human)
DOID:0110545
  • autosomal dominant nonsyndromic deafness 13
  • Aliases:
    • DFNA13
    • autosomal dominant deafness 13
Homo sapiens (human)
DOID:0110544
  • autosomal dominant nonsyndromic deafness 12
  • Aliases:
    • DFNA12
    • DFNA8
    • autosomal dominant deafness 12
    • autosomal dominant deafness 8
Homo sapiens (human)
DOID:0110543
  • autosomal dominant nonsyndromic deafness 11
  • Aliases:
    • DFNA11
    • autosomal dominant deafness 11
Homo sapiens (human)
DOID:0110542
  • autosomal dominant nonsyndromic deafness 10
  • Aliases:
    • DFNA10
    • autosomal dominant deafness 10
Homo sapiens (human)
DOID:0110541
  • autosomal dominant nonsyndromic deafness 1
  • Aliases:
    • DFNA1
    • Konigsmark syndrome
    • LFHL1
    • autosomal dominant deafness 1
    • autosomal dominant deafness 1, with or without thrombocytopenia
    • hereditary low frequency hearing loss 1
Homo sapiens (human)

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Last updated: August 19, 2024