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Factor V Deficiency
Factor v deficiency
Overview
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Coagulation system
(34)
Activated protein C
Antithrombin iii deficiency
Coagulation factor
Factor II deficiency
Factor ix
Factor ix
Factor vii deficiency
Factor viii
Factor x deficiency
Factor xii deficiency
Factor xiii
Fibrinogen
Haemostasis
Protein Z
Protein s
Prothrombin complex
Prothrombinase
TFPI
Tenase
Thrombomodulin
Tissue factor
Von willebrand factor
Bone hemostasis
Clot retraction
Cofact
Des-gamma carboxyprothrombin
Factor XI
Fibrinogenolysis
High-molec- ular-weight kininogen
Human Activated Protein C
Medical Laboratory Scientist
Platelet
Platelet activation
Prekallikrein
Protein Z-related protease inhibitor
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Diseases and disorders
(44)
Fibromuscular dysplasia
Fast breathing
Factor V Leiden
Alpha Thalassemia
Floppy mitral valve
Floppy mitral valve
Fasciitis, necrotizing
Familial spastic paraparesis
Fibrous dysplasia of bone
Agranulocytosis
Familial dysbetalip- oproteinemia
Activated protein c resistance
Fibromyoma
Antiphospholipid syndrome
Haemophilia A
Fish tapeworm
Hematologic disease
Hyperproth- rombinemia
Parahemophilia
Basopenia
Thrombosis
Hyperhomoc- ysteinemia
Hemophilia b
Protein s deficiency
Von willebrand disease
Enzymopathy
Heparin induced thrombocytopenia
Prothrombin deficiency
Factor xi deficiency
Sulfhemoglobinemia
Protein c deficiency
Antithrombin deficiency
Familial paroxysmal polyserositis
Haemophilia
Disseminated intravascular coagulation
Female pseudo-Turner syndrome
Platelet storage pool deficiency
Hypoprocon- vertinemia
Frambesia tropica
Glanzmann thrombasthenia
Factor ix deficiency
Factor x deficiency
Factor vii deficiency
Antithrombin iii deficiency
Factor xii deficiency
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Genetic disorders
(13)
Fibromuscular dysplasia
Alpha Thalassemia
Familial spastic paraparesis
Fibrous dysplasia of bone
Activated protein c resistance
Activated protein c resistance
Haemophilia A
Von willebrand disease
Factor xi deficiency
Antithrombin deficiency
Familial paroxysmal polyserositis
Haemophilia
Female pseudo-Turner syndrome
Glanzmann thrombasthenia
more...
Blood disorders
(128)
Acquired hemolytic anemia
Drug-induced autoimmune hemolytic anemia
Drug-induced nonautoimmune hemolytic anemia
Acute eosinophilic leukemia
Acute lymphoblastic leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid dendritic cell leukemia
Acute myeloid leukemia
Acute promyelocytic leukemia
Adult T-cell leukemia/lymphoma
Aggressive NK-cell leukemia
Agranulocytosis
Alpha Thalassemia
Amyloid purpura
Analbuminaemia
Anaplastic large cell lymphoma
Anemia
Anemia of chronic disease
Anemia of prematurity
Angioimmunoblastic T-cell lymphoma
Antiphospholipid syndrome
Aplastic anemia
Atransferrinemia
Autoimmune hemolytic anemia
Autoimmune neutropenia
B symptoms
Bernard-Soulier syndrome
Beta-thalassemia
Bisalbuminemia
Blood hammer
Cavernous sinus thrombosis
Chemothera- py-induced neutropenia
Chromosome 5q deletion syndrome
Chronic myelogenous leukemia
Chronic neutrophilic leukemia
Congenital amegakaryocytic thrombocytopenia
Congenital dyserythropoietic anemia
Congenital hemolytic anemia
Contaminated haemophilia blood products
Cyclic neutropenia
Deaths from blood disease
Delta-thalassemia
Diamond-Blackfan anemia
Enteropath- y-associated T-cell lymphoma
Eosinopenia
Essential thrombocytosis
Evans syndrome
Factor xi deficiency
Familial dysfibrinogenemia
Glanzmann thrombasthenia
Haemophilia
Haemophilia A
Haemorrhagic and haematological disorders of fetus and newborn
Hairy cell leukemia
Harris platelet syndrome
Hematological malignancy
Hematology
Hemoglobin variants
Hemoglobinemia
Hemolytic anemia
Hemolytic disease of the newborn
Hemolytic disease of the newborn (ABO)
Hemolytic disease of the newborn (anti-Kell)
Hemolytic disease of the newborn (anti-RhE)
Hemolytic disease of the newborn (anti-Rhc)
Hemophagocytic lymphohistiocytosis
Hemophilia b
Hepatosplenic T-cell lymphoma
Hereditary elliptocytosis
Hereditary pyropoikilocytosis
Hereditary spherocytosis
Hodgkin's lymphoma
Hypersegmented neutrophil
Hypochromic anemia
Hypoprothrombinemia
Idiopathic thrombocytopenic purpura
Laminopathy
Large granular lymphocytic leukemia
Leukemia
Leukopenia
Lindsay Tribunal
List of hemophilia organizations
Loxoscelism
Lymphocytopenia
Lymphoma
Macrocytic anemia
Mantle cell lymphoma
Mast cell leukemia
May-Hegglin anomaly
Megaloblastic anemia
Methemoglobinemia
Minimally differentiated acute myeloblastic leukemia
Monoclonal B-cell lymphocytosis
Monoclonal gammopathy of undetermined significance
Myeloid sarcoma
Myelophthisic anemia
Neonatal alloimmune thrombocytopenia
Neutropenia
Nodular lymphocyte predominant Hodgkin's lymphoma
Non-Hodgkin lymphoma
Paroxysmal cold hemoglobinuria
Pel-Ebstein fever
Plummer-Vinson syndrome
Polycythemia vera
Primary effusion lymphoma
Protein s deficiency
Pseudo gray platelet syndrome
Quebec Platelet Disorder
Refractory anemia
Rh disease
Richter's transformation
Scott syndrome
Sickle cell trait
Sickle-cell disease
Spherocytosis
Splenic marginal zone lymphoma
T-cell prolymphocytic leukemia
Thalassemia
Thrombocytopenia
Thrombocytosis
Triosephosphate isomerase deficiency
Vaso-occlusive crisis
Von willebrand disease
Waldenström's macroglobulinemia
Warm autoimmune hemolytic anemia
Wiskott-Aldrich syndrome
Working Formulation
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EC 3.4.21
(29)
Plasmin
Acrosin
Activated protein C
C3-convertase
Chymotrypsin
Chymotrypsin
Elastase
Enteropeptidase
Factor II deficiency
Factor XI
Factor ix
Factor vii deficiency
Factor x deficiency
Factor xii deficiency
Fibrinolysin
Kallikrein
Membrane-bound transcription factor peptidase, site 1
Pancreatic elastase
Prolyl endopeptidase
Prostate-specific antigen
Proteinase 3
Proteinase K
Reelin
Repressor lexA
Serine protease
Tissue plasminogen activator
Trypsin
Trypsin inhibitor
Tryptase
Urokinase
more...
Rheumatology
Lupus anticoagulant
Antiphospholipid syndrome
Familial paroxysmal polyserositis
Blood products
(13)
Cryoprecipitate
Fresh frozen plasma
Blood banks
Blood plasma
Bloodmobile
Bloodmobile
Cofact
Hepatitis B immune globulin
Placenta cord banking
Plasmapheresis
Platelet
Platelet-rich plasma
Prothrombin complex
Whole blood
more...
Symptoms
Umbilical stump bleeding
Bleeding into the skin
Bleeding of the gums
Bruise
Excessive menstrual bleeding
Prolonged bleeding
Fast breathing
Gene
LMAN1
MCFD2
Thrombomodulin
Medical signs
APTT
Bleeding disorder
Bandemia
Hematology
(23)
Thrombophilia
Venous thrombosis
Fondaparinux
Monocytopenia
Argatroban
Argatroban
Factor V Leiden
Drug-induced nonautoimmune hemolytic anemia
Activated protein C
Activated protein c resistance
Drug-induced autoimmune hemolytic anemia
Acquired hemolytic anemia
Antiphospholipid syndrome
Hematologic disease
Thrombosis
Lupus anticoagulant
Von willebrand factor
Haemostasis
Heparin induced thrombocytopenia
Protein c deficiency
Cryoprecipitate
Bleeding disorder
Disseminated intravascular coagulation
Thrombotic thrombocytopenic purpura
more...
Signs and tests
Bleeding time
Factor V assay
Prolonged prothrombin time
Partial thromboplastin time
See also
(20)
Familial hypertrigl- yceridemia
Cytosis
Immune disorders
Penia
Fibrosing alveolitis
Fibrosing alveolitis
Myeloid
Fenestrations
Procoagulant
Thromboprophylaxis
ADAMTS8
Malignancy
Vitamin k deficiency
Novoseven
Familial
Br. J. Haematol.
Prothrombin mutation
Hereditary
Fibrinolysis
MTHFR
Factor 5
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