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 15751 - 15775 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0050453
  • lissencephaly
Xenopus laevis (African clawed frog)
DOID:0050453
  • lissencephaly
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Rattus norvegicus (Norway rat)
DOID:0050453
  • lissencephaly
Saccharomyces cerevisiae S288C
DOID:0050453
  • lissencephaly
Drosophila melanogaster (fruit fly)
DOID:0050453
  • lissencephaly
Xenopus tropicalis (tropical clawed frog)
DOID:0050453
  • lissencephaly
Mus musculus (house mouse)
DOID:0050453
  • lissencephaly
Danio rerio (zebrafish)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Rattus norvegicus (Norway rat)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Homo sapiens (human)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Mus musculus (house mouse)
DOID:0050451
  • Brugada syndrome
  • Aliases:
    • Bangungut
    • Brugada type idiopathic ventricular fibrillation
    • Dream disease
    • Pokkuri death syndrome
    • SUNDS
    • sudden unexplained nocturnal death syndrome
Homo sapiens (human)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Mus musculus (house mouse)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Xenopus laevis (African clawed frog)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Rattus norvegicus (Norway rat)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Homo sapiens (human)
DOID:0050449
  • pachyonychia congenita
  • Aliases:
    • Jackson-Lawler Type Pachyonychia Congenita
    • Jadassohn-Lewandowsky Syndrome
    • PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE
    • Pachyonychia Congenita Type 1
Homo sapiens (human)
DOID:0050448
  • white sponge nevus
  • Aliases:
    • hereditary mucosal leukokeratosis
    • white sponge nevus of Cannon
Homo sapiens (human)
DOID:0050445
  • X-linked dominant hypophosphatemic rickets
  • Aliases:
    • Hypophosphatemia, Vitamin D-Resistant Rickets
    • Vitamin D-Resistant Rickets, X-Linked
    • X-linked hypophosphatemia
    • hypophosphatemic rickets X-linked dominant
Homo sapiens (human)
DOID:0050445
  • X-linked dominant hypophosphatemic rickets
  • Aliases:
    • Hypophosphatemia, Vitamin D-Resistant Rickets
    • Vitamin D-Resistant Rickets, X-Linked
    • X-linked hypophosphatemia
    • hypophosphatemic rickets X-linked dominant
Caenorhabditis elegans
DOID:0050445
  • X-linked dominant hypophosphatemic rickets
  • Aliases:
    • Hypophosphatemia, Vitamin D-Resistant Rickets
    • Vitamin D-Resistant Rickets, X-Linked
    • X-linked hypophosphatemia
    • hypophosphatemic rickets X-linked dominant
Mus musculus (house mouse)
DOID:0050445
  • X-linked dominant hypophosphatemic rickets
  • Aliases:
    • Hypophosphatemia, Vitamin D-Resistant Rickets
    • Vitamin D-Resistant Rickets, X-Linked
    • X-linked hypophosphatemia
    • hypophosphatemic rickets X-linked dominant
Drosophila melanogaster (fruit fly)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Homo sapiens (human)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Mus musculus (house mouse)
DOID:0050440
  • familial partial lipodystrophy
  • Aliases:
    • Dunnigan Syndrome
    • Koberling-Dunnigan Syndrome
Rattus norvegicus (Norway rat)

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Last updated: August 19, 2024