| Condition | Indicated | Relationship Strength | Studies | Trials |
|---|
Heritable Pulmonary Arterial Hypertension
[description not available] | 0 | 5.95 | 5 | 1 |
Anoxemia
[description not available] | 0 | 2.41 | 1 | 0 |
Disease Models, Animal
Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 4.29 | 6 | 0 |
Pulmonary Hypertension
[description not available] | 0 | 7.35 | 5 | 2 |
Innate Inflammatory Response
[description not available] | 0 | 2.41 | 1 | 0 |
Pulmonary Arterial Hypertension
A progressive rare pulmonary disease characterized by high blood pressure in the PULMONARY ARTERY. | 0 | 8.77 | 18 | 3 |
Hypoxia
Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 2.41 | 1 | 0 |
Hypertension, Pulmonary
Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 7.35 | 5 | 2 |
Inflammation
A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function. | 0 | 2.41 | 1 | 0 |
Familial Primary Pulmonary Hypertension
Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease. | 0 | 5.95 | 5 | 1 |
Anemia
A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 16.95 | 15 | 9 |
Disease Exacerbation
[description not available] | 0 | 3.51 | 2 | 0 |
Cryptogenic Fibrosing Alveolitis
[description not available] | 0 | 3.52 | 1 | 0 |
Idiopathic Pulmonary Fibrosis
A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 3.52 | 1 | 0 |
Anemia With Multinucleated Erythroblasts
[description not available] | 0 | 2.25 | 1 | 0 |
Thrombopenia
[description not available] | 0 | 4.62 | 1 | 1 |
Thrombocytopenia
A subnormal level of BLOOD PLATELETS. | 0 | 4.62 | 1 | 1 |
Chronic Kidney Diseases
[description not available] | 0 | 3.95 | 2 | 0 |
Renal Insufficiency, Chronic
Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002) | 0 | 3.95 | 2 | 0 |
Thalassemias
[description not available] | 0 | 3.06 | 1 | 0 |
Thalassemia
A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. | 0 | 3.06 | 1 | 0 |
Dysmyelopoietic Syndromes
[description not available] | 0 | 8.84 | 6 | 4 |
Myelodysplastic Syndromes
Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA. | 0 | 8.84 | 6 | 4 |
Anemia, Cooley's
[description not available] | 0 | 9.17 | 9 | 4 |
beta-Thalassemia
A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. | 0 | 9.17 | 9 | 4 |
Anemia, Congenital Hypoplastic, Of Blackfan And Diamond
[description not available] | 0 | 3.46 | 2 | 0 |
Anemia, Diamond-Blackfan
A rare congenital hypoplastic anemia that usually presents early in infancy. The disease is characterized by a moderate to severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone marrow with erythroid hypoplasia, and an increased risk of developing leukemia. (Curr Opin Hematol 2000 Mar;7(2):85-94) | 0 | 3.46 | 2 | 0 |
Kahler Disease
[description not available] | 0 | 5.72 | 2 | 1 |
Bone Diseases
Diseases of BONES. | 0 | 3.01 | 1 | 0 |
Multiple Myeloma
A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 5.72 | 2 | 1 |
Hemoglobinopathies
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. | 0 | 3.01 | 1 | 0 |
Osteolysis
Dissolution of bone that particularly involves the removal or loss of calcium. | 0 | 4.4 | 1 | 1 |
Hypercoagulability
[description not available] | 0 | 2.1 | 1 | 0 |
A-Thalassemia
[description not available] | 0 | 2.1 | 1 | 0 |
Hemoglobinuria
The presence of free HEMOGLOBIN in the URINE, indicating hemolysis of ERYTHROCYTES within the vascular system. After saturating the hemoglobin-binding proteins (HAPTOGLOBINS), free hemoglobin begins to appear in the urine. | 0 | 2.1 | 1 | 0 |
alpha-Thalassemia
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. | 0 | 2.1 | 1 | 0 |
Iron Overload
An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 3.43 | 2 | 0 |
Thrombophilia
A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 2.1 | 1 | 0 |
Bone Cancer
[description not available] | 0 | 3.01 | 1 | 0 |
Breast Cancer
[description not available] | 0 | 10.73 | 2 | 1 |
Bone Neoplasms
Tumors or cancer located in bone tissue or specific BONES. | 0 | 3.01 | 1 | 0 |
Breast Neoplasms
Tumors or cancer of the human BREAST. | 0 | 5.73 | 2 | 1 |
Bone Loss, Osteoclastic
[description not available] | 0 | 7.47 | 4 | 4 |
Low Bone Density
[description not available] | 0 | 2.05 | 1 | 0 |
Bone Diseases, Metabolic
Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 2.05 | 1 | 0 |