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 1076 - 1100 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:0110577
  • autosomal dominant nonsyndromic deafness 51
  • Aliases:
    • DFNA51
    • autosomal dominant deafness 51
    • chromosome 9q21.11 duplication syndrome
Homo sapiens (human)
DOID:0110578
  • autosomal dominant nonsyndromic deafness 52
  • Aliases:
    • DFNA52
    • autosomal dominant deafness 52
Homo sapiens (human)
DOID:0110579
  • autosomal dominant nonsyndromic deafness 53
  • Aliases:
    • DFNA53
    • autosomal dominant deafness 53
Homo sapiens (human)
DOID:0110580
  • autosomal dominant nonsyndromic deafness 54
  • Aliases:
    • DFNA54
    • autosomal dominant deafness 54
Homo sapiens (human)
DOID:0110581
  • autosomal dominant nonsyndromic deafness 56
  • Aliases:
    • DFNA56
    • autosomal dominant deafness 56
Homo sapiens (human)
DOID:0110582
  • autosomal dominant nonsyndromic deafness 58
  • Aliases:
    • DFNA58
    • autosomal dominant deafness 58
Homo sapiens (human)
DOID:0110583
  • autosomal dominant nonsyndromic deafness 59
  • Aliases:
    • DFNA59
    • autosomal dominant deafness 59
Homo sapiens (human)
DOID:0110584
  • autosomal dominant nonsyndromic deafness 6
  • Aliases:
    • DFNA14
    • DFNA38
    • DFNA6
    • autosomal dominant deafness 14
    • autosomal dominant deafness 38
    • autosomal dominant deafness 6
Homo sapiens (human)
DOID:0110585
  • autosomal dominant nonsyndromic deafness 64
  • Aliases:
    • DFNA64
    • autosomal dominant deafness 64
Homo sapiens (human)
DOID:0110586
  • autosomal dominant nonsyndromic deafness 65
  • Aliases:
    • DFNA65
    • autosomal dominant deafness 65
Homo sapiens (human)
DOID:0110587
  • autosomal dominant nonsyndromic deafness 66
  • Aliases:
    • DFNA66
    • autosomal dominant deafness 66
Homo sapiens (human)
DOID:0110588
  • autosomal dominant nonsyndromic deafness 67
  • Aliases:
    • DFNA67
    • autosomal dominant deafness 67
Homo sapiens (human)
DOID:0110589
  • autosomal dominant nonsyndromic deafness 68
  • Aliases:
    • DFNA68
    • autosomal dominant deafness 68
Homo sapiens (human)
DOID:0110590
  • autosomal dominant nonsyndromic deafness 69
  • Aliases:
    • DCUA
    • DFNA69
    • autosomal dominant deafness 69
    • unilateral or asymmetric congenital deafness
Homo sapiens (human)
DOID:0110591
  • autosomal dominant nonsyndromic deafness 7
  • Aliases:
    • DFNA7
    • autosomal dominant deafness 7
Homo sapiens (human)
DOID:0110592
  • autosomal dominant nonsyndromic deafness 70
  • Aliases:
    • DFNA70
    • autosomal dominant deafness 70
Homo sapiens (human)
DOID:0112160
  • autosomal dominant nonsyndromic deafness 79
  • Aliases:
    • DFNA79
Homo sapiens (human)
DOID:0110593
  • autosomal dominant nonsyndromic deafness 9
  • Aliases:
    • DFNA9
    • autosomal dominant deafness 9
Homo sapiens (human)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Homo sapiens (human)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Homo sapiens (human)
DOID:0110938
  • autosomal dominant osteopetrosis 2
  • Aliases:
    • Albers-Schonberg osteopetrosis
    • OPTA2
    • autosomal dominant Albers-Schonberg disease
    • autosomal dominant osteopetrosis type II
    • osteopetrosis autosomal dominant type 2
Homo sapiens (human)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Homo sapiens (human)
DOID:0060855
  • autosomal dominant pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1A
    • autosomal dominant PHA 1
Homo sapiens (human)
DOID:0060764
  • autosomal recessive Robinow syndrome
  • Aliases:
    • COVESDEM syndrome
    • RRS
    • costovertebral segmentation defect-mesomelia syndrome
Homo sapiens (human)
DOID:0111216
  • autosomal recessive centronuclear myopathy
  • Aliases:
    • AR-CNM
Homo sapiens (human)

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Last updated: August 19, 2024