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 1151 - 1175 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:0110292
  • autosomal recessive limb-girdle muscular dystrophy type 2O
  • Aliases:
    • LGMD2O
    • MDDGC3
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
    • muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related
Homo sapiens (human)
DOID:0110293
  • autosomal recessive limb-girdle muscular dystrophy type 2P
  • Aliases:
    • LGMD2P
    • MDDGC9
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
    • muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
Homo sapiens (human)
DOID:0110285
  • autosomal recessive limb-girdle muscular dystrophy type 2Q
  • Aliases:
    • LGMD2Q
    • autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
    • muscular dystrophy, limb-girdle, type 2Q
Homo sapiens (human)
DOID:0110287
  • autosomal recessive limb-girdle muscular dystrophy type 2S
  • Aliases:
    • LGMD2S
    • muscular dystrophy, limb-girdle, type 2S
Homo sapiens (human)
DOID:0110294
  • autosomal recessive limb-girdle muscular dystrophy type 2T
  • Aliases:
    • LGMD2T
    • MDDGC14
    • muscular dystrophy limb-girdle type 2T
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
    • muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
Homo sapiens (human)
DOID:0110295
  • autosomal recessive limb-girdle muscular dystrophy type 2U
  • Aliases:
    • LGMD2U
    • MDDGC7
    • autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency
    • muscular dystrophy limb-girdle type 2U
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C7
Homo sapiens (human)
DOID:0110289
  • autosomal recessive limb-girdle muscular dystrophy type 2Y
  • Aliases:
    • LGMD2Y
    • autosomal recessive muscular dystrophy due to LAP1B deficiency
    • autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency
    • muscular dystrophy with progressive weakness, distal contractures and rigid spine
    • muscular dystrophy, limb-girdle, type 2Y
Homo sapiens (human)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Homo sapiens (human)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Homo sapiens (human)
DOID:0110462
  • autosomal recessive nonsyndromic deafness 101
  • Aliases:
    • DFNB101
    • autosomal recessive deafness 101
Homo sapiens (human)
DOID:0110463
  • autosomal recessive nonsyndromic deafness 102
  • Aliases:
    • DFNB102
    • autosomal recessive deafness 102
Homo sapiens (human)
DOID:0110464
  • autosomal recessive nonsyndromic deafness 103
  • Aliases:
    • DFNB103
    • autosomal recessive deafness 103
Homo sapiens (human)
DOID:0110465
  • autosomal recessive nonsyndromic deafness 104
  • Aliases:
    • DFNB104
    • autosomal recessive deafness 104
Homo sapiens (human)
DOID:0110467
  • autosomal recessive nonsyndromic deafness 12
  • Aliases:
    • DFNB12
    • autosomal recessive deafness 12
Homo sapiens (human)
DOID:0110468
  • autosomal recessive nonsyndromic deafness 13
  • Aliases:
    • DFNB13
    • autosomal recessive deafness 13
Homo sapiens (human)
DOID:0110469
  • autosomal recessive nonsyndromic deafness 14
  • Aliases:
    • DFNB14
    • autosomal recessive deafness 14
Homo sapiens (human)
DOID:0110470
  • autosomal recessive nonsyndromic deafness 15
  • Aliases:
    • DFNB15
    • DFNB72
    • DFNB95
    • autosomal recessive deafness 15
    • autosomal recessive deafness 72
    • autosomal recessive deafness 95
Homo sapiens (human)
DOID:0110471
  • autosomal recessive nonsyndromic deafness 16
  • Aliases:
    • DFNB16
    • autosomal recessive deafness 16
Homo sapiens (human)
DOID:0110472
  • autosomal recessive nonsyndromic deafness 17
  • Aliases:
    • DFNB17
    • autosomal recessive deafness 17
Homo sapiens (human)
DOID:0110473
  • autosomal recessive nonsyndromic deafness 18A
  • Aliases:
    • DFNB18A
    • autosomal recessive deafness 18A
Homo sapiens (human)
DOID:0110474
  • autosomal recessive nonsyndromic deafness 18B
  • Aliases:
    • DFNB18B
    • autosomal recessive deafness 18B
Homo sapiens (human)
DOID:0110475
  • autosomal recessive nonsyndromic deafness 1A
  • Aliases:
    • DFNB1A
    • autosomal recessive deafness 1A
Homo sapiens (human)
DOID:0110476
  • autosomal recessive nonsyndromic deafness 1B
  • Aliases:
    • DFNB1B
    • autosomal recessive deafness 1B
Homo sapiens (human)
DOID:0110477
  • autosomal recessive nonsyndromic deafness 2
  • Aliases:
    • DFNB2
    • autosomal recessive deafness 2
Homo sapiens (human)
DOID:0110478
  • autosomal recessive nonsyndromic deafness 20
  • Aliases:
    • DFNB20
    • autosomal recessive deafness 20
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024