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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 12001 - 12025 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0070248
  • autosomal recessive Emery-Dreifuss muscular dystrophy 3
  • Aliases:
    • EDMD3
    • Emery-Dreifuss muscular dystrophy 3, autosomal recessive
Rattus norvegicus (Norway rat)
DOID:0070248
  • autosomal recessive Emery-Dreifuss muscular dystrophy 3
  • Aliases:
    • EDMD3
    • Emery-Dreifuss muscular dystrophy 3, autosomal recessive
Mus musculus (house mouse)
DOID:0110033
  • autosomal recessive Alport syndrome
Mus musculus (house mouse)
DOID:0110033
  • autosomal recessive Alport syndrome
Homo sapiens (human)
DOID:0110033
  • autosomal recessive Alport syndrome
Caenorhabditis elegans
DOID:0110033
  • autosomal recessive Alport syndrome
Drosophila melanogaster (fruit fly)
DOID:0111900
  • autosomal dominant thrombophilia due to protein S deficiency
  • Aliases:
    • THPH5
Homo sapiens (human)
DOID:0111900
  • autosomal dominant thrombophilia due to protein S deficiency
  • Aliases:
    • THPH5
Mus musculus (house mouse)
DOID:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Rattus norvegicus (Norway rat)
DOID:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Homo sapiens (human)
DOID:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Mus musculus (house mouse)
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
Mus musculus (house mouse)
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
Homo sapiens (human)
DOID:0060855
  • autosomal dominant pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1A
    • autosomal dominant PHA 1
Homo sapiens (human)
DOID:0111517
  • autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
  • Aliases:
    • PEOA2
    • autosomal dominant progressive external ophthalmoplegia 2
Rattus norvegicus (Norway rat)
DOID:0111517
  • autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
  • Aliases:
    • PEOA2
    • autosomal dominant progressive external ophthalmoplegia 2
Mus musculus (house mouse)
DOID:0111517
  • autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
  • Aliases:
    • PEOA2
    • autosomal dominant progressive external ophthalmoplegia 2
Homo sapiens (human)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Mus musculus (house mouse)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Rattus norvegicus (Norway rat)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Homo sapiens (human)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Drosophila melanogaster (fruit fly)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Caenorhabditis elegans
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Danio rerio (zebrafish)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Homo sapiens (human)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Mus musculus (house mouse)
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Last updated: December 9, 2024