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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 14851 - 14875 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0060366
  • Hennekam syndrome
  • Aliases:
    • Hennekam lymphangiectasia-lymphedema syndrome
    • lymphedem-lymphangiectasia-intellectual disability syndrome
Homo sapiens (human)
DOID:0060366
  • Hennekam syndrome
  • Aliases:
    • Hennekam lymphangiectasia-lymphedema syndrome
    • lymphedem-lymphangiectasia-intellectual disability syndrome
Danio rerio (zebrafish)
DOID:0060366
  • Hennekam syndrome
  • Aliases:
    • Hennekam lymphangiectasia-lymphedema syndrome
    • lymphedem-lymphangiectasia-intellectual disability syndrome
Mus musculus (house mouse)
DOID:0070408
  • Hengel-Maroofian-Schols syndrome
Mus musculus (house mouse)
DOID:0070058
  • Helsmoortel-Van Der Aa Syndrome
  • Aliases:
    • HVDAS
    • MRD28
    • autosomal dominant mental retardation 28
Homo sapiens (human)
DOID:0070058
  • Helsmoortel-Van Der Aa Syndrome
  • Aliases:
    • HVDAS
    • MRD28
    • autosomal dominant mental retardation 28
Mus musculus (house mouse)
DOID:0111363
  • Heinz body anemia
Mus musculus (house mouse)
DOID:0111363
  • Heinz body anemia
Saccharomyces cerevisiae S288C
DOID:0111363
  • Heinz body anemia
Homo sapiens (human)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Rattus norvegicus (Norway rat)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Homo sapiens (human)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Mus musculus (house mouse)
DOID:0081395
  • Harel-Yoon syndrome
  • Aliases:
    • Ocular anomalies-axonal neuropathy-developmental delay syndrome
Homo sapiens (human)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Caenorhabditis elegans
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Rattus norvegicus (Norway rat)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Drosophila melanogaster (fruit fly)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Homo sapiens (human)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Mus musculus (house mouse)
DOID:0070539
  • Halperin-Birk syndrome
  • Aliases:
    • HLBKS
    • NEDSOSB
    • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Saccharomyces cerevisiae S288C
DOID:0070539
  • Halperin-Birk syndrome
  • Aliases:
    • HLBKS
    • NEDSOSB
    • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Homo sapiens (human)
DOID:0070539
  • Halperin-Birk syndrome
  • Aliases:
    • HLBKS
    • NEDSOSB
    • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Mus musculus (house mouse)
DOID:2736
  • Hajdu-Cheney syndrome
  • Aliases:
    • Cheney syndrome
    • HJCYS
    • SFPKS
    • acroosteolysis with osteoporosis and changes in skull and mandible
    • arthrodentoosteodysplasia
    • serpentine fibula-polycystic kidney syndrome
Caenorhabditis elegans
DOID:2736
  • Hajdu-Cheney syndrome
  • Aliases:
    • Cheney syndrome
    • HJCYS
    • SFPKS
    • acroosteolysis with osteoporosis and changes in skull and mandible
    • arthrodentoosteodysplasia
    • serpentine fibula-polycystic kidney syndrome
Mus musculus (house mouse)
DOID:2736
  • Hajdu-Cheney syndrome
  • Aliases:
    • Cheney syndrome
    • HJCYS
    • SFPKS
    • acroosteolysis with osteoporosis and changes in skull and mandible
    • arthrodentoosteodysplasia
    • serpentine fibula-polycystic kidney syndrome
Homo sapiens (human)
DOID:2736
  • Hajdu-Cheney syndrome
  • Aliases:
    • Cheney syndrome
    • HJCYS
    • SFPKS
    • acroosteolysis with osteoporosis and changes in skull and mandible
    • arthrodentoosteodysplasia
    • serpentine fibula-polycystic kidney syndrome
Drosophila melanogaster (fruit fly)
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Last updated: December 9, 2024