| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Amegakaryocytic thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Megakaryocytic thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| May-Hegglin-anomalie |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
3 |
| syndrome d'Epstein |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
4 |
| Montreal platelet syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Mediterranean thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Post-splenectomy thrombocytosis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| pseudoziekte van von Willebrand |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
3 |
| pancytopenie-dysmeliesyndroom |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
5 |
| Essential thrombocythemia (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Parvoviral aplastic crisis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
7 |
| Thrombocytosis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Aplastic anaemia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
7 |
| Platelet dysfunction associated with uremia (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Aplastic anaemia due to infection |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
8 |
| Hereditary thrombocytopenic disorder (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Autoimmune neonatal thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Wiskott-Aldrich autosomal dominant variant syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Thrombocytopenia due to sequestration |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Neonatal thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Medich giant platelet syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Attenuated Chédiak-Higashi syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Familial thrombocytosis (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Revesz syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
9 |
| Congenital amegakaryocytic thrombocytopenia (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Acquired platelet disorder |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Chronic acquired pure red cell aplasia |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
6 |
| Aplastic anemia caused by antineoplastic agent |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
7 |
| X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
7 |
| Pancytopenia due to IKZF1 mutations |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
6 |
| Macrothrombocytopenia with mitral valve insufficiency |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Bleeding disorder due to glycoprotein VI deficiency (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Ataxia pancytopenia syndrome |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
6 |
| Thrombocytopenia due to COVID-19 |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
4 |
| Familial pigmented purpuric eruption |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
5 |
| Fetal thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Fetal hemophilia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Upshaw-Schulman syndrome (disorder) |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Autoimmune thrombotic thrombocytopenic purpura (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
5 |
| Acquired thrombotic thrombocytopenic purpura (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
5 |
| Drug induced thrombotic thrombocytopenic purpura (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Deficiency of coagulation factor due to vitamin K malabsorption (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Factor X deficiency due to systemic amyloidosis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Drug-induced fibrinolytic disorder |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Fibrinolytic disorder caused by tissue plasminogen activator |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Fibrinolytic disorder caused by urokinase |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Pancytopenia caused by anticonvulsant |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Pancytopenia caused by antithyroid drug (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Vaccine-induced prothrombotic immune thrombocytopenia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| X-linked thrombocytopenia with normal platelets (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Acquired prekallikrein deficiency (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Hereditary congenital prekallikrein deficiency (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Hereditary thrombocytopenia with early-onset myelofibrosis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Antepartum hemorrhage with afibrinogenemia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Hyperfibrinolysis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Antepartum hemorrhage with coagulation defect (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Antepartum haemorrhage with hyperfibrinolysis |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| hémorragie en antepartum avec défaut de coagulation, mère ayant accouché |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
2 |
| hémorragie en antepartum avec défaut de coagulation, mère n'ayant pas encore accouché |
Interprets |
False |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Antepartum hemorrhage with hypofibrinogenemia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Antepartum hemorrhage with disseminated intravascular coagulation (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Maternal perinatal purpura (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Fetal purpura (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Autosomal dominant thrombocytopenia with platelet secretion defect |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Severe autosomal recessive macrothrombocytopenia (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Acquired antithrombin III deficiency |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Premature separation of placenta with coagulation defect |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Thrombomodulin-related bleeding disorder (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Congenital autosomal recessive small-platelet thrombocytopenia (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Acquired protein S deficiency |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Acquired protein C deficiency (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Acquired heparin cofactor II deficiency (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Intrapartum hemorrhage with coagulation defect |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Parturient hemorrhage associated with hypofibrinogenemia |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Postpartum afibrinogenemia with hemorrhage |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
4 |
| Pigmented purpuric dermatosis (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
5 |
| Lichen aureus (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
6 |
| Progressive pigmentary dermatosis of Schamberg |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
6 |
| Upshaw-Schulman syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
2 |
| Hereditary von Willebrand disease |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Hematopoietic subsyndrome of acute radiation syndrome (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Afibrinogenemia following molar pregnancy (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
4 |
| Afibrinogenemia following ectopic pregnancy (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
4 |
| Defibrination syndrome following molar pregnancy |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Defibrination syndrome following ectopic pregnancy (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
3 |
| Fanconi anemia of complementation group C |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
7 |
| Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Mild hereditary factor VIII deficiency disease with low response inhibitor |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder) |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Severe hereditary factor VIII deficiency disease with low response inhibitor |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Moderate hereditary factor VIII deficiency disease with high response inhibitor |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |
| Moderate hereditary factor VIII deficiency disease with low response inhibitor |
Interprets |
True |
Hemostatic function |
Inferred relationship |
Some |
1 |