Also known as: Owren Parahemophilia, Owren disease, Parahemophilia, Proaccelerin deficiency, congenital factor V deficiency, deficiency, labile, factor 5 deficiency, factor V deficiency, hereditary Factor V deficiency, hereditary factor V deficiency, hereditary hypoproaccelerinaemia, labile Factor deficiency, labile factor deficiency
Also known as: F7 deficiency, congenital factor VII deficiency, congenital proconvertin deficiency, factor 7 deficiency, factor VII deficiency, hypoproconvertinemia
Also known as: F10 deficiency, Stuart factor deficiency, congenital, Stuart-Prower Factor deficiency, Stuart-Prower factor deficiency, congenital Stuart factor deficiency, congenital factor X deficiency, disease, Stuart-Prower, factor 10 deficiency, factor X deficiency, factor X deficiency, congenital, hereditary Factor X deficiency
Also known as: F11 deficiency, PTA deficiency, Rosenthal factor deficiency, Rosenthal syndrome, Rosenthal's disease, congenital factor XI deficiency, factor 11 deficiency, factor XI deficiency, factor XI deficiency, autosomal dominant, factor XI deficiency, autosomal recessive, haemophilia C, hemophilia C, hereditary Factor XI deficiency, hereditary factor XI deficiency, hereditary factor XI deficiency disease, plasma thromboplastin antecedent deficiency
Also known as: deficiency, Laki-Lorand factor, factor XIII deficiency, factor XIII deficiency disease, fibrin stabilising factor deficiency, fibrin stabilizing factor deficiency, fibrin-stabilizing factor deficiency, hereditary factor XIII deficiency disease
Also known as: CFTDM, congenital fiber type disproportion, congenital fiber-type disproportion, congenital fibre type disproportion, congenital myopathy with fiber type disproportion, congenital myopathy with fibre type disproportion, myopathy, congenital with fiber-type disproportion
Also known as: congenital fibrinogen deficiency, fibrinogen deficiency, congenital
Also known as: CFEOM1, Feom1 locus, KIF21A congenital fibrosis of extraocular muscles, blepharoptosis with absent eye movements, congenital fibrosis of extraocular muscles caused by mutation in KIF21A, fibrosis of extraocular muscles, congenital, 1, fibrosis of extraocular muscles, congenital, 3B, ophthalmoplegia, congenital
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