Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Severe fever with thrombocytopenia syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Thrombocytopenia co-occurrent and due to alcoholism (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Doan-Wright syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Acquired pancytopenia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Evans syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Thrombotic thrombocytopenic purpura |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pancytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pancytopenia with pancreatitis |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pancytopenia-dysmelia |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Upshaw-Schulman syndrome (disorder) |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune thrombotic thrombocytopenic purpura (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acquired thrombotic thrombocytopenic purpura (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Drug induced thrombotic thrombocytopenic purpura (disorder) |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fanconi's anemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Estren-Dameshek anaemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autoimmune pancytopenia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Isolated thrombocytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Refractory thrombocytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Thyrocerebrorenal syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Pancytopenia caused by medication |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Congenital thrombocytopaenia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Inherited predisposition to essential thrombocythemia |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Thrombocytosis |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Essential thrombocythemia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Familial thrombocytosis (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Post-splenectomy thrombocytosis |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Reactive thrombocytosis |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pancytopenia due to antineoplastic chemotherapy |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Diarrhea-negative hemolytic uremic syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acquired red cell aplasia |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aplastic anemia due to radiation |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Aplastic anaemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Constitutional aplastic anaemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
WT limb blood syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hemolytic uremic syndrome of childhood |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Diarrhea-associated hemolytic uremic syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Congenital hemolytic uremic syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Aplastic anemia due to toxic cause (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Hemolytic uremic syndrome, adult type |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Haemolytic uraemic syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Parvoviral aplastic crisis |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aplastic anemia associated with pregnancy (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Familial haemolytic uraemic syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Aplastic anemia caused by antineoplastic agent |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Pure red cell aplasia, acquired |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Constitutional aplastic anemia with malformation |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Aplastic anemia due to chronic disease |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acquired aplastic anemia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Idiopathic aplastic anaemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Revesz syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Aplastic anemia associated with metabolic alteration (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Immunologic aplastic anemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Secondary aplastic anemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Aplastic anaemia due to drugs |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aplastic anemia associated with pancreatitis (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Transient acquired pure red cell aplasia |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aplastic anaemia due to infection |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic acquired pure red cell aplasia |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Adult pure red cell aplasia (disorder) |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Humoral immunologic aplastic anemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Cellular immunologic aplastic anemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Ataxia pancytopenia syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Kasabach-Merritt syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare haemorrhagic disorder due to a platelet anomaly characterised by dysfunctional platelets of abnormally large size, moderate thrombocytopenia, prolonged bleeding time and mild bleeding diathesis (ecchymoses and epistaxis), associated with mitral valve insufficiency. |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Thrombocythemia with distal limb defect |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare genetic hematologic disorder characterized by progressive trilineage bone marrow failure (with hypocellularity), developmental delay with learning disabilities and microcephaly. Mild facial dysmorphism and hypotonia have also been reported. There is evidence the disease is caused by homozygous mutation in the ERCC6L2 gene on chromosome 9q22. |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary thrombocytopenia with normal platelets (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary isolated aplastic anemia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Pancytopenia due to IKZF1 mutations |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pancytopenia caused by immunosuppressant |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Atypical haemolytic uraemic syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Thrombocytopenia due to severe acute respiratory syndrome coronavirus 2 (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fetal thrombocytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Upshaw-Schulman syndrome (disorder) |
Interprets |
False |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Drug induced thrombotic thrombocytopenic purpura (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Pancytopenia caused by anticonvulsant |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Pancytopenia caused by antithyroid drug (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Vaccine-induced prothrombotic immune thrombocytopenia |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
X-linked thrombocytopenia with normal platelets (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percentage reticulated platelet count |
Is a |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Hereditary thrombocytopenia with early-onset myelofibrosis |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal dominant thrombocytopenia with platelet secretion defect |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Severe autosomal recessive macrothrombocytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital autosomal recessive small-platelet thrombocytopenia (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Upshaw-Schulman syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Hematopoietic subsyndrome of acute radiation syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Haemolytic uraemic syndrome with DGKE deficiency |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Infection-related hemolytic uremic syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Fanconi anemia of complementation group C |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Pancytopenia caused by colchicine (disorder) |
Interprets |
True |
Platelet count |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |