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 1876 - 1900 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:0110228
  • cataract 8 multiple types
  • Aliases:
    • CCV
    • CTRCT8
    • cataract, congenital, Volkmann type
Homo sapiens (human)
DOID:0110246
  • cataract 26 multiple types
  • Aliases:
    • CTRCT26
Homo sapiens (human)
DOID:0110231
  • cataract 1 multiple types
  • Aliases:
    • CTRCT1
    • Duffy linked cataract
    • cataract 1, multiple types, with or without microcornea
Homo sapiens (human)
DOID:0110265
  • cataract 31 multiple types
  • Aliases:
    • CTRCT31
Homo sapiens (human)
DOID:0110260
  • cataract 7
  • Aliases:
    • CTRCT7
Homo sapiens (human)
DOID:0110254
  • cataract 25
  • Aliases:
    • CCSSO
    • CTRCT25
    • central pouch-like cataract with sutural opacities
    • central saccular cataract with sutural opacities
    • early-onset cataract with Y-shaped suture opacities
Homo sapiens (human)
DOID:0110241
  • cataract 41
  • Aliases:
    • CTRCT41
    • congenital nuclear type cataract 41
Homo sapiens (human)
DOID:0110251
  • cataract 15 multiple types
  • Aliases:
    • CTRCT15
Homo sapiens (human)
DOID:0110236
  • cataract 39 multiple types
  • Aliases:
    • CTRCT39
    • autosomal dominant cataract 39 multiple types
Homo sapiens (human)
DOID:0110230
  • cataract 34 multiple types
  • Aliases:
    • CATC3
    • CTRCT34
    • autosomal recessive congenital cataract 3
    • cataract 34 multiple types with or without microcornea
Homo sapiens (human)
DOID:0110243
  • cataract 46 juvenile-onset
  • Aliases:
    • CTRCT46
    • juvenilae cataract Hutterite type
Homo sapiens (human)
DOID:0110256
  • cataract 21 multiple types
  • Aliases:
    • CTRCT21
    • cataract 21 multiple types with or without microcornea
Homo sapiens (human)
DOID:0110249
  • cataract 11 multiple types
  • Aliases:
    • CTRCT11
Homo sapiens (human)
DOID:0110232
  • cataract 29
  • Aliases:
    • cataract 29 coralliform
Homo sapiens (human)
DOID:0110233
  • cataract 27
  • Aliases:
    • CTRCT27
    • cataract 27 nuclear progressive
Homo sapiens (human)
DOID:0110250
  • cataract 16 multiple types
  • Aliases:
    • CTRCT16
Homo sapiens (human)
DOID:0110237
  • cataract 42
  • Aliases:
    • CTRCT42
Homo sapiens (human)
DOID:2566
  • corneal dystrophy
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Homo sapiens (human)
DOID:0080335
  • mitochondrial DNA depletion syndrome 12b
Homo sapiens (human)
DOID:0080132
  • Sengers syndrome
  • Aliases:
    • mitochondrial DNA depletion syndrome 10
    • mitochondrial DNA depletion syndrome 10 (cardiomyopathic type)
Homo sapiens (human)
DOID:0111135
  • congenital generalized lipodystrophy type 1
  • Aliases:
    • Berardinelli-Seip Congenital Lipodystrophy, Type 1
    • Brunzell syndrome AGPAT2-related
Homo sapiens (human)
DOID:811
  • lipodystrophy
Homo sapiens (human)
DOID:11712
  • lipoatrophic diabetes mellitus
  • Aliases:
    • lipoatrophic diabetes
Homo sapiens (human)
DOID:0111138
  • congenital generalized lipodystrophy type 4
  • Aliases:
    • Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy
    • congenital generalised lipodystrophy type 4
    • generalised congenital lipodystrophy type 4
    • generalised congenital lipodystrophy with myopathy
    • generalized congenital lipodystrophy type 4
    • generalized congenital lipodystrophy with myopathy
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: August 19, 2024