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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 13601 - 13625 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Rattus norvegicus (Norway rat)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Homo sapiens (human)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Mus musculus (house mouse)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Drosophila melanogaster (fruit fly)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Rattus norvegicus (Norway rat)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Mus musculus (house mouse)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Homo sapiens (human)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Xenopus laevis (African clawed frog)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Danio rerio (zebrafish)
DOID:0111008
  • X-linked cone-rod dystrophy 1
  • Aliases:
    • COD1
    • CORDX1
    • X-linked cone dystrophy 1
Mus musculus (house mouse)
DOID:0080681
  • X-linked chronic idiopathic intestinal pseudo-obstruction
Homo sapiens (human)
DOID:0070195
  • X-linked chronic granulomatous disease
  • Aliases:
    • CDGX
    • X-linked chronic cytochrome b-negative granulomatous disease
Homo sapiens (human)
DOID:0070195
  • X-linked chronic granulomatous disease
  • Aliases:
    • CDGX
    • X-linked chronic cytochrome b-negative granulomatous disease
Mus musculus (house mouse)
DOID:0080352
  • X-linked chondrodysplasia punctata 2
  • Aliases:
    • Conradi-Hunermann Syndrome
    • Happle syndrome
Homo sapiens (human)
DOID:0080352
  • X-linked chondrodysplasia punctata 2
  • Aliases:
    • Conradi-Hunermann Syndrome
    • Happle syndrome
Mus musculus (house mouse)
DOID:0060292
  • X-linked chondrodysplasia punctata 1
  • Aliases:
    • chondrodystrophia calcificans congenita
Mus musculus (house mouse)
DOID:0060292
  • X-linked chondrodysplasia punctata 1
  • Aliases:
    • chondrodystrophia calcificans congenita
Homo sapiens (human)
DOID:0111765
  • X-linked cardiac valvular dysplasia
  • Aliases:
    • CVD1
    • Dystrophie valvulaire associee a FLNA
    • EDS 5
    • Ehlers-Danlos syndrome, type 5
    • FLNA-related X-linked myxomatous valvular dysplasia
    • FLNA-related valvular dystrophy
    • Filamin A-related X-linked myxomatous valvular dysplasia
    • XMVD
Homo sapiens (human)
DOID:0112157
  • X-linked atrophic macular degeneration
Mus musculus (house mouse)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Rattus norvegicus (Norway rat)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Mus musculus (house mouse)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Homo sapiens (human)
DOID:0080156
  • X-linked adrenal hypoplasia congenita
  • Aliases:
    • congenital adrenal hypoplasia
Homo sapiens (human)
DOID:0111766
  • X-linked VACTERL association
  • Aliases:
    • VACTERL association, X-linked with or without hydrocephalus
    • VACTERLX
Mus musculus (house mouse)
DOID:0070251
  • X-linked Emery-Dreifuss muscular dystrophy 6
  • Aliases:
    • EDMD6
    • Emery-Dreifuss muscular dystrophy 6, X-linked
    • XMPMA
    • myopathy, X-linked, with postural muscle atrophy
Homo sapiens (human)
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Last updated: December 9, 2024