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 6801 - 6825 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0060672
  • Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
Mus musculus (house mouse)
DOID:0111706
  • oblique facial clefting 1
  • Aliases:
    • Tessier number 4 facial cleft
Mus musculus (house mouse)
DOID:13689
  • prostate calculus
  • Aliases:
    • Prostatic lithiasis
    • Prostatic stone
    • Stone of prostate
    • calculus of prostate
Mus musculus (house mouse)
DOID:0110347
  • osteogenesis imperfecta type 15
  • Aliases:
    • OI15
    • osteogenesis imperfecta type XV
Mus musculus (house mouse)
DOID:12120
  • pulmonary alveolar proteinosis
Mus musculus (house mouse)
DOID:0090030
  • corticosteroid-binding globulin deficiency
  • Aliases:
    • CBG deficiency
    • transcortin deficiency
Mus musculus (house mouse)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Mus musculus (house mouse)
DOID:2384
  • Wernicke encephalopathy
  • Aliases:
    • Wernicke's disease
    • Wernicke's encephalopathy
Mus musculus (house mouse)
DOID:0110476
  • autosomal recessive nonsyndromic deafness 1B
  • Aliases:
    • DFNB1B
    • autosomal recessive deafness 1B
Mus musculus (house mouse)
DOID:0111249
  • uveal coloboma-cleft lip and palate-intellectual disability
  • Aliases:
    • COB1
    • Uveal coloboma-cleft lip/palate-mental retardation syndrome
    • coloboma-microphthalmos syndrome
    • coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate
    • ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation
Mus musculus (house mouse)
DOID:0111776
  • 46,XY sex reversal 5
  • Aliases:
    • 46,XY gonadal dysgenesis, complete, CBX2-related
    • 46,XY sex reversal, CBX2-related
    • SRXY5
    • disorder of sex development, 46,XY, CBX2-related
    • sex reversal, XY, CBX2-related
Mus musculus (house mouse)
DOID:9620
  • vesicoureteral reflux
  • Aliases:
    • vesico-ureteral reflux
Mus musculus (house mouse)
DOID:0081394
  • Caroli syndrome
Mus musculus (house mouse)
DOID:1930
  • Laurence-Moon syndrome
  • Aliases:
    • LNMS
Mus musculus (house mouse)
DOID:8955
  • sideroblastic anemia
  • Aliases:
    • ANEMIA SIDEROBLASTIC
    • Anemia, hypochromic with iron loading
Mus musculus (house mouse)
DOID:0050827
  • rheumatic heart disease
  • Aliases:
    • rheumatic carditis
Mus musculus (house mouse)
DOID:9008
  • psoriatic arthritis
  • Aliases:
    • arthritis psoriatica
    • arthropathic psoriasis
Mus musculus (house mouse)
DOID:0110915
  • childhood hypophosphatasia
Mus musculus (house mouse)
DOID:9065
  • leishmaniasis
Mus musculus (house mouse)
DOID:13365
  • reading disorder
Mus musculus (house mouse)
DOID:0060569
  • hypertrichotic osteochondrodysplasia Cantu type
  • Aliases:
    • Cantu syndrome
Mus musculus (house mouse)
DOID:0111533
  • gnathodiaphyseal dysplasia
  • Aliases:
    • GDD
    • Levin syndrome 2
    • gnathodiaphyseal sclerosis
    • osteogenesis imperfecta with unusual skeletal lesions
    • osteogenesis imperfecta, Levin type
Mus musculus (house mouse)
DOID:3981
  • pantothenate kinase-associated neurodegeneration
  • Aliases:
    • Hallervorden-Spatz disease
    • Hallervorden-Spatz syndrome
    • NBIA1
    • Pigmentary pallidal degeneration
    • brain Iron Accumulation type I syndrome
    • neurodegeneration with brain iron accumulation 1
Mus musculus (house mouse)
DOID:4762
  • vasculogenic impotence
Mus musculus (house mouse)
DOID:0110123
  • Bardet-Biedl syndrome 1
  • Aliases:
    • BBS1
Mus musculus (house mouse)

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Last updated: December 9, 2024