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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 1901 - 1925 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0110221
  • Brugada syndrome 4
  • Aliases:
    • BRGDA4
Homo sapiens (human)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Homo sapiens (human)
DOID:0110223
  • Brugada syndrome 6
  • Aliases:
    • BRGDA6
Homo sapiens (human)
DOID:0110224
  • Brugada syndrome 7
  • Aliases:
    • BRGDA7
Homo sapiens (human)
DOID:0110225
  • Brugada syndrome 8
  • Aliases:
    • BRGDA8
Homo sapiens (human)
DOID:0110229
  • cataract 6 multiple types
  • Aliases:
    • CTRCT6
Homo sapiens (human)
DOID:0110241
  • cataract 41
  • Aliases:
    • CTRCT41
    • congenital nuclear type cataract 41
Homo sapiens (human)
DOID:0110242
  • cataract 13 with adult i phenotype
  • Aliases:
    • CTRCT13
Homo sapiens (human)
DOID:0110243
  • cataract 46 juvenile-onset
  • Aliases:
    • CTRCT46
    • juvenilae cataract Hutterite type
Homo sapiens (human)
DOID:0110245
  • cataract 38
  • Aliases:
    • CATC5
    • CTRCT38
    • autosomal recessive congenital cataract 5
Homo sapiens (human)
DOID:0110247
  • cataract 36
  • Aliases:
    • CATC4
    • CTRCT36
    • autosomal recessive congenital cataract 4
Homo sapiens (human)
DOID:0110248
  • cataract 30
  • Aliases:
    • CTRCT30
    • Dusty cataract
    • cataract 30 pulverulent
    • cataract Coppock-like
Homo sapiens (human)
DOID:0110250
  • cataract 16 multiple types
  • Aliases:
    • CTRCT16
Homo sapiens (human)
DOID:0110255
  • cataract 5 multiple types
  • Aliases:
    • CTRCT5
Homo sapiens (human)
DOID:0110262
  • cataract 45
  • Aliases:
    • CTRCT45
Homo sapiens (human)
DOID:0110263
  • cataract 19 multiple types
  • Aliases:
    • CTRCT19
Homo sapiens (human)
DOID:0110264
  • cataract 33
  • Aliases:
    • CTRCT33
Homo sapiens (human)
DOID:0110265
  • cataract 31 multiple types
  • Aliases:
    • CTRCT31
Homo sapiens (human)
DOID:0110266
  • cataract 9 multiple types
  • Aliases:
    • CTRCT9
    • cataract 9 multiple types with or without microcornea
Homo sapiens (human)
DOID:0110267
  • cataract 44
  • Aliases:
    • CTRCT44
    • total early-onset cataract
Homo sapiens (human)
DOID:0110272
  • cataract 40
  • Aliases:
    • CTRCT40
    • cataract 40 X-linked
    • cataract 40 with or without microcornea
Homo sapiens (human)
DOID:0110273
  • autosomal dominant limb-girdle muscular dystrophy
Homo sapiens (human)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Homo sapiens (human)
DOID:0110275
  • autosomal recessive limb-girdle muscular dystrophy type 2A
  • Aliases:
    • LGMD2A
    • Leyden-Moebius muscular dystrophy
    • limb-girdle muscular dystrophy due to calpain deficiency
    • muscular dystrophy, limb-girdle, type 2A
    • pelvofemoral muscular dystrophy
    • primary calpainopathy
Homo sapiens (human)
DOID:0110277
  • autosomal recessive limb-girdle muscular dystrophy type 2C
  • Aliases:
    • DMDA1
    • LGMD2C
    • Maghrebian myopathy
    • SCARMD
    • autosomal recessive Duchenne-like muscular dystrophy type 1
    • deficiency of sarcoglycan gamma
    • gamma-sarcoglycanopathy
    • limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency
    • muscular dystrophy, limb-girdle, type 2C
    • severe childhood autosomal recessive muscular dystrophy North African type
Homo sapiens (human)
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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

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Last updated: December 9, 2024