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 6526 - 6550 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0060850
  • annular pancreas
Homo sapiens (human)
DOID:0060772
  • multiple types of congenital heart defects 6
  • Aliases:
    • DTGA3
    • dextro-looped transposition of the great arteries 3
Homo sapiens (human)
DOID:0070418
  • vertebral hypersegmentation and orofacial anomalies
  • Aliases:
    • VHO
Homo sapiens (human)
DOID:0080591
  • Klippel-Feil syndrome 3
Homo sapiens (human)
DOID:0060838
  • isolated microphthalmia 7
  • Aliases:
    • MCOP7
Homo sapiens (human)
DOID:0110964
  • brachydactyly type A1
  • Aliases:
    • BDA1
    • Farabee type brachydactyly
Homo sapiens (human)
DOID:0081317
  • multiple synostoses syndrome 1
Homo sapiens (human)
DOID:0110970
  • brachydactyly type C
  • Aliases:
    • BDC
Homo sapiens (human)
DOID:0080788
  • proximal symphalangism 2
Homo sapiens (human)
DOID:0080052
  • acromesomelic dysplasia, Grebe type
  • Aliases:
    • acromesomelic dysplasia-2A
    • grebe chondrodysplasia
Homo sapiens (human)
DOID:0060931
  • developmental dysplasia of the hip 1
  • Aliases:
    • DDH1
Homo sapiens (human)
DOID:0081318
  • multiple synostoses syndrome 2
Homo sapiens (human)
DOID:0080051
  • acromesomelic dysplasia, Hunter-Thompson type
  • Aliases:
    • acromesomelic dwarfism
    • acromesomelic dysplasia-2C
Homo sapiens (human)
DOID:0110977
  • brachydactyly type A1C
  • Aliases:
    • BDA1C
Homo sapiens (human)
DOID:0050790
  • fibular hypoplasia and complex brachydactyly
  • Aliases:
    • Du Pan syndrome
    • acromesomelic dysplasia-2B
Homo sapiens (human)
DOID:0081320
  • multiple synostoses syndrome 4
Homo sapiens (human)
DOID:0080589
  • Klippel-Feil syndrome 1
Homo sapiens (human)
DOID:0060836
  • isolated microphthalmia 4
  • Aliases:
    • MCOP4
Homo sapiens (human)
DOID:0110217
  • Leber congenital amaurosis 17
  • Aliases:
    • LCA17
Homo sapiens (human)
DOID:0080871
  • primary ovarian insufficiency 14
Homo sapiens (human)
DOID:3049
  • Churg-Strauss syndrome
  • Aliases:
    • Allergic Granulomatous Angiitis
    • Allergic granulomatosis angiitis
    • Churg-Strauss vasculitis
Homo sapiens (human)
DOID:440
  • neuromuscular disease
Homo sapiens (human)
DOID:0081263
  • neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
  • Aliases:
    • NEDMCR syndrome
Homo sapiens (human)
DOID:0070443
  • neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
Homo sapiens (human)
DOID:4252
  • Alexander disease
  • Aliases:
    • Alexander's disease
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024