Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Autoimmune haemolytic anaemia, cold type (Q39539) (← links)
- Evans syndrome (Q39540) (← links)
- Acquired haemolytic anaemia, immune (Q39541) (← links)
- Microangiopathic haemolytic anaemia (Q39542) (← links)
- Paroxysmal cold haemoglobinuria (Q39543) (← links)
- Autoimmune haemolytic anaemia, warm type (Q39544) (← links)
- Haemolytic uraemic syndrome (Q39545) (← links)
- Paroxysmal nocturnal haemoglobinuria (Q39546) (← links)
- Acquired pure red cell aplasia (Q39547) (← links)
- Chronic acquired pure red cell aplasia (Q39548) (← links)
- Acute acquired pure red cell aplasia (Q39549) (← links)
- Acquired aplastic anaemias (Q39550) (← links)
- Congenital aplastic anaemia (Q39551) (← links)
- Congenital pure red cell aplasia (Q39552) (← links)
- Congenital non-inherited pure red cell aplasia (Q39553) (← links)
- Hereditary pure red cell aplasia (Q39554) (← links)
- Drug-induced aplastic anaemia (Q39555) (← links)
- Aplastic anaemia due to other external agents (Q39556) (← links)
- Idiopathic aplastic anaemia (Q39557) (← links)
- Transient abnormal myelopoiesis (Q39558) (← links)
- Acute posthaemorrhagic anaemia (Q39559) (← links)
- Anaemia in chronic infectious diseases (Q39560) (← links)
- Anaemia in neoplastic disease (Q39561) (← links)
- Anaemia in chronic kidney disease (Q39562) (← links)
- 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)
