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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 2426 - 2450 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0111019
  • cone-rod dystrophy 12
  • Aliases:
    • CORD12
Homo sapiens (human)
DOID:0111017
  • cone-rod dystrophy 10
  • Aliases:
    • CORD10
Homo sapiens (human)
DOID:0111015
  • Newfoundland cone-rod dystrophy
  • Aliases:
    • NFRCD
Homo sapiens (human)
DOID:0111013
  • cone-rod dystrophy 3
  • Aliases:
    • CORD3
Homo sapiens (human)
DOID:0111011
  • cone-rod dystrophy 6
  • Aliases:
    • CORD6
    • RCD2
    • retinal cone dystrophy 2
Homo sapiens (human)
DOID:0111010
  • cone-rod dystrophy 5
  • Aliases:
    • CORD5
Homo sapiens (human)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Homo sapiens (human)
DOID:0111004
  • Joubert syndrome 9
  • Aliases:
    • JBTS9
Homo sapiens (human)
DOID:0111002
  • Joubert syndrome 7
  • Aliases:
    • JBTS7
Homo sapiens (human)
DOID:0111001
  • Joubert syndrome 6
  • Aliases:
    • JBTS6
Homo sapiens (human)
DOID:0110995
  • Joubert syndrome 26
  • Aliases:
    • JBTS26
Homo sapiens (human)
DOID:0110994
  • Joubert syndrome 25
  • Aliases:
    • JBTS25
Homo sapiens (human)
DOID:0110993
  • Joubert syndrome 24
  • Aliases:
    • JBTS24
Homo sapiens (human)
DOID:0110989
  • Joubert syndrome 20
  • Aliases:
    • JBTS20
Homo sapiens (human)
DOID:0110987
  • Joubert syndrome 18
  • Aliases:
    • JBTS18
Homo sapiens (human)
DOID:0110985
  • Joubert syndrome 16
  • Aliases:
    • JBTS16
Homo sapiens (human)
DOID:0110984
  • Joubert syndrome 15
  • Aliases:
    • JBTS15
Homo sapiens (human)
DOID:0110982
  • Joubert syndrome 13
  • Aliases:
    • JBTS13
Homo sapiens (human)
DOID:0110980
  • Joubert syndrome 1
  • Aliases:
    • CORS1
    • CPD4
    • JBTS1
    • cerebellooculorenal syndrome 1
    • cerebelloparenchymal disorder IV
Homo sapiens (human)
DOID:0110978
  • brachydactyly type A1D
  • Aliases:
    • BDA1D
Homo sapiens (human)
DOID:0110977
  • brachydactyly type A1C
  • Aliases:
    • BDA1C
Homo sapiens (human)
DOID:0110976
  • brachydactyly type E2
  • Aliases:
    • BDE2
Homo sapiens (human)
DOID:0110975
  • brachydactyly type B2
  • Aliases:
    • BDB2
Homo sapiens (human)
DOID:0110972
  • brachydactyly type E1
  • Aliases:
    • BDE1
Homo sapiens (human)
DOID:0110971
  • brachydactyly type D
  • Aliases:
    • BDD
Homo sapiens (human)
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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