Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- Anaemia due to chronic disease (Q39563) (← links)
- Sideroblastic anaemia (Q39564) (← links)
- Acquired sideroblastic anaemias (Q39565) (← links)
- Congenital sideroblastic anaemias (Q39566) (← links)
- Hereditary sideroblastic anaemias (Q39567) (← links)
- Hereditary syndromic sideroblastic anaemia (Q39568) (← links)
- Congenital dyserythropoietic anaemia (Q39569) (← links)
- Anaemia due to acute disease (Q39570) (← links)
- Aplastic anaemia (Q39571) (← links)
- Disseminated intravascular coagulation (Q39572) (← links)
- Hereditary factor VIII deficiency with anti-factor VIII inhibitor (Q39573) (← links)
- Haemophilia A (Q39574) (← links)
- Hereditary factor VIII deficiency (Q39575) (← links)
- Hereditary factor IX deficiency (Q39576) (← links)
- Haemophilia B (Q39577) (← links)
- Thrombophilia (Q39578) (← links)
- Von Willebrand disease (Q39579) (← links)
- Haemophilia C (Q39580) (← links)
- Hereditary factor X deficiency (Q39581) (← links)
- Hereditary deficiency of factor I (Q39582) (← links)
- Inherited coagulation factor deficiency without bleeding tendency (Q39583) (← links)
- Other inherited coagulation factor deficiency with bleeding tendency (Q39584) (← links)
- Combined deficiency of vitamin K-dependent clotting factors (Q39585) (← links)
- Haemorrhage due to thrombin inhibitor other than heparin (Q39586) (← links)
- Haemorrhagic disorder due to circulating anticoagulants or coagulation factors inhibitors (Q39587) (← links)
- Haemorrhage due to factor Xa inhibitor (Q39588) (← links)
- Acquired haemophilia (Q39589) (← links)
- Hereditary thrombophilia (Q39591) (← links)
- Hyperhomocysteinaemia (Q39593) (← links)
- Primary antiphospholipid syndrome (Q39595) (← links)
- Acquired thrombophilia (Q39597) (← links)
- Antiphospholipid syndrome (Q39599) (← links)
- Secondary antiphospholipid syndrome (Q39601) (← links)
- Lupus anticoagulant-hypoprothrombinaemia syndrome (Q39603) (← links)
- Antiphospholipid syndrome in pregnancy (Q39605) (← links)
- Congenital alpha-2 antiplasmin deficiency (Q39606) (← links)
- Congenital plasminogen activator inhibitor type 1 deficiency (Q39607) (← links)
- Inherited fibrinolytic defects (Q39608) (← links)
- Drug-induced vasculitis (Q39609) (← links)
- IgA vasculitis (Q39610) (← links)
- Bleeding diathesis due to thromboxane synthesis deficiency (Q39612) (← links)
- Alpha-delta dense granule deficiency (Q39613) (← links)
- Inherited qualitative platelet defects (Q39614) (← links)
- Dense granule disease (Q39615) (← links)
- Qualitative platelet defects (Q39616) (← links)
- Isolated thrombocytopenia (Q39617) (← links)
- Alpha-granule diseases (Q39618) (← links)
- Inherited giant platelet disorder (Q39619) (← links)
- Non-thrombocytopenic purpura (Q39620) (← links)
- Hereditary vascular purpura (Q39621) (← links)
