Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- 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)
- Traumatic purpura (Q39622) (← links)
- Acquired vascular purpura (Q39623) (← links)
- Immune thrombocytopenic purpura (Q39624) (← links)
- Drug-induced thrombocytopenic purpura (Q39625) (← links)
- Alloimmune thrombocytopenia (Q39626) (← links)
- Secondary thrombocytopenic purpura (Q39627) (← links)
- Drug-induced cytopenia (Q39628) (← links)
- Acquired thrombocytopenia (Q39629) (← links)
- Thrombocytopenia (Q39630) (← links)
- Hereditary thrombocytopenia (Q39631) (← links)
- Congenital thrombocytopenia (Q39632) (← links)
- Congenital non-inherited thrombocytopenia (Q39633) (← links)
- Purpura or bruising due to disorders of coagulation (Q39634) (← links)
- Neutrophil immunodeficiency syndrome (Q39635) (← links)
- Functional neutrophil defects (Q39636) (← links)
- Constitutional neutrophilia (Q39637) (← links)
- Constitutional disorders of neutrophil function (Q39638) (← links)
