GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1951 - 1975 of 7942 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:0110530
  • autosomal recessive nonsyndromic deafness 84B
  • Aliases:
    • DFNB84B
    • autosomal recessive deafness 84B
Homo sapiens (human)
DOID:0110531
  • autosomal recessive nonsyndromic deafness 85
  • Aliases:
    • DFNB85
    • autosomal recessive deafness 85
Homo sapiens (human)
DOID:0110532
  • autosomal recessive nonsyndromic deafness 86
  • Aliases:
    • DFNB86
    • autosomal recessive deafness 86
Homo sapiens (human)
DOID:0110533
  • autosomal recessive nonsyndromic deafness 88
  • Aliases:
    • DFNB88
    • autosomal recessive deafness 88
Homo sapiens (human)
DOID:0110534
  • autosomal recessive nonsyndromic deafness 89
  • Aliases:
    • DFNB89
    • autosomal recessive deafness 89
Homo sapiens (human)
DOID:0110535
  • autosomal recessive nonsyndromic deafness 9
  • Aliases:
    • DFNB9
    • NRSD9
    • autosomal recessive deafness 9
    • neurosensory nonsyndromic recessive deafness 9
Homo sapiens (human)
DOID:0110536
  • autosomal recessive nonsyndromic deafness 91
  • Aliases:
    • DFNB91
    • autosomal recessive deafness 91
Homo sapiens (human)
DOID:0110537
  • autosomal recessive nonsyndromic deafness 93
  • Aliases:
    • DFNB93
    • autosomal recessive deafness 93
Homo sapiens (human)
DOID:0110538
  • autosomal recessive nonsyndromic deafness 96
  • Aliases:
    • DFNB96
    • autosomal recessive deafness 96
Homo sapiens (human)
DOID:0110539
  • autosomal recessive nonsyndromic deafness 97
  • Aliases:
    • DFNB97
    • autosomal recessive deafness 97
Homo sapiens (human)
DOID:0110540
  • autosomal recessive nonsyndromic deafness 98
  • Aliases:
    • DFNB98
    • autosomal recessive deafness 98
Homo sapiens (human)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Homo sapiens (human)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Drosophila melanogaster (fruit fly)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Caenorhabditis elegans
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Mus musculus (house mouse)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Danio rerio (zebrafish)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Xenopus tropicalis (tropical clawed frog)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Xenopus laevis (African clawed frog)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Rattus norvegicus (Norway rat)
DOID:0110942
  • autosomal recessive osteopetrosis 1
  • Aliases:
    • OPTB1
    • autosomal recessive Albers-Schonberg disease
    • infantile malignant osteopetrosis 1
Homo sapiens (human)
DOID:0110946
  • autosomal recessive osteopetrosis 7
  • Aliases:
    • OPTB7
    • autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • autosomal recessive osteopetrosis type 7
    • osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • osteopetrosis-hypogammaglobulinemia syndrome
Homo sapiens (human)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Rattus norvegicus (Norway rat)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Mus musculus (house mouse)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Homo sapiens (human)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Homo sapiens (human)

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Last updated: August 19, 2024