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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 2351 - 2375 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111089
  • Fanconi anemia complementation group D1
  • Aliases:
    • FAD1
    • FANCD1
Homo sapiens (human)
DOID:0111094
  • Fanconi anemia complementation group N
  • Aliases:
    • FANCN
Homo sapiens (human)
DOID:0111096
  • Fanconi anemia complementation group O
  • Aliases:
    • FANCO
Homo sapiens (human)
DOID:0111098
  • Fanconi anemia complementation group B
  • Aliases:
    • FACB
    • FANCB
    • Fanconi pancytopenia type 2
Homo sapiens (human)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Homo sapiens (human)
DOID:0111102
  • maturity-onset diabetes of the young type 3
  • Aliases:
    • MODY type 3
    • MODY3
Homo sapiens (human)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Homo sapiens (human)
DOID:0111105
  • maturity-onset diabetes of the young type 8
  • Aliases:
    • MODY type 8
    • MODY8
    • diabetes and pancreatic exocrine
    • maturity-onset diabetes of the young type 8 with exocrine dysfunction
Homo sapiens (human)
DOID:0111108
  • maturity-onset diabetes of the young type 10
  • Aliases:
    • MODY10
Homo sapiens (human)
DOID:0111110
  • maturity-onset diabetes of the young type 13
  • Aliases:
    • MODY type 13
    • MODY13
Homo sapiens (human)
DOID:0111111
  • maturity-onset diabetes of the young type 14
  • Aliases:
    • MODY14
Homo sapiens (human)
DOID:0111113
  • nephronophthisis 2
  • Aliases:
    • NPH2
    • NPHP2
    • infantile nephronophthisis 2
Homo sapiens (human)
DOID:0111114
  • nephronophthisis 3
  • Aliases:
    • NPH3
    • NPHP3
Homo sapiens (human)
DOID:0111118
  • nephronophthisis 11
  • Aliases:
    • NPHP11
Homo sapiens (human)
DOID:0111122
  • nephronophthisis 14
  • Aliases:
    • NPHP14
Homo sapiens (human)
DOID:0111123
  • nephronophthisis 15
  • Aliases:
    • NPHP15
Homo sapiens (human)
DOID:0111127
  • nephronophthisis 20
  • Aliases:
    • NPHP20
Homo sapiens (human)
DOID:0111128
  • focal segmental glomerulosclerosis 1
  • Aliases:
    • FSGS1
Homo sapiens (human)
DOID:0111129
  • focal segmental glomerulosclerosis 2
  • Aliases:
    • FSGS2
Homo sapiens (human)
DOID:0111130
  • focal segmental glomerulosclerosis 5
  • Aliases:
    • FSGS5
Homo sapiens (human)
DOID:0111131
  • focal segmental glomerulosclerosis 6
  • Aliases:
    • FSGS6
Homo sapiens (human)
DOID:0111133
  • focal segmental glomerulosclerosis 8
  • Aliases:
    • FSGS8
Homo sapiens (human)
DOID:0111134
  • focal segmental glomerulosclerosis 9
  • Aliases:
    • FSGS9
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:0111136
  • congenital generalized lipodystrophy type 2
  • Aliases:
    • Berardinelli-Seip congenital lipodystrophy type 2
    • Berardinelli-Seip syndrome
    • Brunzell syndrome BSCL2-related
    • CGL2
    • congenital lipoatrophic diabetes
    • total lipodystrophy and acromegaloid gigantism
Homo sapiens (human)
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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