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 7801 - 7825 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111905
  • autosomal recessive thrombophilia due to protein S deficiency
  • Aliases:
    • THPH6
    • autosomal recessive thrombophilia due to congenital protein S deficiency
    • severe hereditary thrombophilia due to congenital protein S deficiency
Mus musculus (house mouse)
DOID:0111905
  • autosomal recessive thrombophilia due to protein S deficiency
  • Aliases:
    • THPH6
    • autosomal recessive thrombophilia due to congenital protein S deficiency
    • severe hereditary thrombophilia due to congenital protein S deficiency
Homo sapiens (human)
DOID:0111904
  • autosomal recessive thrombophilia due to protein C deficiency
  • Aliases:
    • THPH4
    • autosomal recessive PROC deficiency
    • autosomal recessive protein C deficiency
Homo sapiens (human)
DOID:0111904
  • autosomal recessive thrombophilia due to protein C deficiency
  • Aliases:
    • THPH4
    • autosomal recessive PROC deficiency
    • autosomal recessive protein C deficiency
Rattus norvegicus (Norway rat)
DOID:0111904
  • autosomal recessive thrombophilia due to protein C deficiency
  • Aliases:
    • THPH4
    • autosomal recessive PROC deficiency
    • autosomal recessive protein C deficiency
Mus musculus (house mouse)
DOID:0111903
  • thrombophilia due to HRG deficiency
  • Aliases:
    • THPH11
    • hereditary thrombophilia due to congenital HRG deficiency
    • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Mus musculus (house mouse)
DOID:0111903
  • thrombophilia due to HRG deficiency
  • Aliases:
    • THPH11
    • hereditary thrombophilia due to congenital HRG deficiency
    • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Homo sapiens (human)
DOID:0111903
  • thrombophilia due to HRG deficiency
  • Aliases:
    • THPH11
    • hereditary thrombophilia due to congenital HRG deficiency
    • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Rattus norvegicus (Norway rat)
DOID:0111902
  • thrombophilia due to activated protein C resistance
  • Aliases:
    • APC resistance
    • PCCF deficiency
    • PROC cofactor deficiency
    • THPH2
    • activated protein C resistance
    • thrombophilia V
    • thrombophilia due to deficiency of activated protein C cofactor
Homo sapiens (human)
DOID:0111902
  • thrombophilia due to activated protein C resistance
  • Aliases:
    • APC resistance
    • PCCF deficiency
    • PROC cofactor deficiency
    • THPH2
    • activated protein C resistance
    • thrombophilia V
    • thrombophilia due to deficiency of activated protein C cofactor
Mus musculus (house mouse)
DOID:0111902
  • thrombophilia due to activated protein C resistance
  • Aliases:
    • APC resistance
    • PCCF deficiency
    • PROC cofactor deficiency
    • THPH2
    • activated protein C resistance
    • thrombophilia V
    • thrombophilia due to deficiency of activated protein C cofactor
Rattus norvegicus (Norway rat)
DOID:0111901
  • heparin cofactor II deficiency
  • Aliases:
    • HCF 2 deficiency
    • HCF II deficiency
    • THPH10
    • thrombophilia due to heparin cofactor II deficiency
Rattus norvegicus (Norway rat)
DOID:0111901
  • heparin cofactor II deficiency
  • Aliases:
    • HCF 2 deficiency
    • HCF II deficiency
    • THPH10
    • thrombophilia due to heparin cofactor II deficiency
Homo sapiens (human)
DOID:0111901
  • heparin cofactor II deficiency
  • Aliases:
    • HCF 2 deficiency
    • HCF II deficiency
    • THPH10
    • thrombophilia due to heparin cofactor II deficiency
Mus musculus (house mouse)
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:0111899
  • X-linked thrombophilia due to factor IX defect
  • Aliases:
    • THPH8
Mus musculus (house mouse)
DOID:0111899
  • X-linked thrombophilia due to factor IX defect
  • Aliases:
    • THPH8
Homo sapiens (human)
DOID:0111899
  • X-linked thrombophilia due to factor IX defect
  • Aliases:
    • THPH8
Rattus norvegicus (Norway rat)
DOID:0111898
  • CK syndrome
  • Aliases:
    • X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
Homo sapiens (human)
DOID:0111896
  • Diamond-Blackfan anemia 18
  • Aliases:
    • DBA18
    • RPL18-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:0111892
  • Diamond-Blackfan anemia 11
  • Aliases:
    • DBA11
    • RPL26-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:0111892
  • Diamond-Blackfan anemia 11
  • Aliases:
    • DBA11
    • RPL26-related Diamond-Blackfan anemia
Mus musculus (house mouse)
DOID:0111888
  • Diamond-Blackfan anemia 10
  • Aliases:
    • DBA10
    • RPS26-related Diamond-Blackfan anemia
Mus musculus (house mouse)
DOID:0111887
  • Diamond-blackfan anemia 3
  • Aliases:
    • DBA3
    • RPS24-related Diamond-Blackfan anemia
Homo sapiens (human)

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Last updated: December 9, 2024