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Browse result for Congenital afibrinogenemia

※ introduction

    A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I).

Reference
DiseaseOntology: Congenital afibrinogenemia


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01463P026712243
FGA
Fibrinogen alpha chain [Cleaved into: Fibrinopeptide A; Fibrinogen alpha chain]
Homo sapiens
PTMD01464P026792266
FGG
Fibrinogen gamma chain
Homo sapiens
PTMD03671P026752244
FGB
Fibrinogen beta chain [Cleaved into: Fibrinopeptide B; Fibrinogen beta chain]
Homo sapiens