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※ introduction

    Haemophilia, or hemophilia[6] (from Ancient Greek ¦Á?¦Ì¦Á (ha?ma) 'blood', and ¦Õ¦É¦Ë?¦Á (phil¨ªa) 'love of'),[7] is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.[2][3] This results in people bleeding for a longer time after an injury, easy bruising, and an increased risk of bleeding inside joints or the brain.[1] Those with a mild case of the disease may have symptoms only after an accident or during surgery.[1] Bleeding into a joint can result in permanent damage while bleeding in the brain can result in long term headaches, seizures, or a altered level of consciousness.[1]

Reference
Wiki: Hemophilia



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01458P004512157
F8
Coagulation factor VIII [Cleaved into: Factor VIIIa heavy chain, 200 kDa isoform; Factor VIIIa heavy chain, 92 kDa isoform; Factor VIII B chain; Factor VIIIa light chain]
Homo sapiens
PTMD03594P007402158
F9
Coagulation factor IX [Cleaved into: Coagulation factor IXa light chain; Coagulation factor IXa heavy chain]
Homo sapiens