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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 7851 - 7875 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0111305
  • familial febrile seizures 4
  • Aliases:
    • FEB4
    • familial febrile convulsions 4
Homo sapiens (human)
DOID:0111310
  • familial febrile seizures 2
  • Aliases:
    • FEB2
    • familial febrile convulsions 2
Rattus norvegicus (Norway rat)
DOID:0111310
  • familial febrile seizures 2
  • Aliases:
    • FEB2
    • familial febrile convulsions 2
Mus musculus (house mouse)
DOID:0111310
  • familial febrile seizures 2
  • Aliases:
    • FEB2
    • familial febrile convulsions 2
Homo sapiens (human)
DOID:0111308
  • familial febrile seizures 11
  • Aliases:
    • FEB11
    • familial febrile convulsions 11
Mus musculus (house mouse)
DOID:0111308
  • familial febrile seizures 11
  • Aliases:
    • FEB11
    • familial febrile convulsions 11
Homo sapiens (human)
DOID:0111308
  • familial febrile seizures 11
  • Aliases:
    • FEB11
    • familial febrile convulsions 11
Saccharomyces cerevisiae S288C
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Homo sapiens (human)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Mus musculus (house mouse)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Homo sapiens (human)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Saccharomyces cerevisiae S288C
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Mus musculus (house mouse)
DOID:0111631
  • familial erythrocytosis 7
  • Aliases:
    • ECYT7
    • alpha-globin type erythrocytosis
    • alpha-globin type polycythemia
Homo sapiens (human)
DOID:0111632
  • familial erythrocytosis 6
  • Aliases:
    • ECYT6
    • beta-globin type erythrocytosis
    • beta-globin type polycythemia
Homo sapiens (human)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Danio rerio (zebrafish)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Rattus norvegicus (Norway rat)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Homo sapiens (human)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Mus musculus (house mouse)
DOID:0080339
  • familial erythrocytosis 4
  • Aliases:
    • ECYT4
Homo sapiens (human)
DOID:0080338
  • familial erythrocytosis 3
  • Aliases:
    • ECYT3
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Homo sapiens (human)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Xenopus laevis (African clawed frog)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Mus musculus (house mouse)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Homo sapiens (human)
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Last updated: December 9, 2024