Condition | Indicated | Relationship Strength | Studies | Trials |
Asthma, Bronchial [description not available] | 0 | 3.17 | 1 | 0 |
Cardiac Failure [description not available] | 0 | 3.17 | 1 | 0 |
Benign Neoplasms [description not available] | 0 | 3.44 | 2 | 0 |
Blood Clot [description not available] | 0 | 3.17 | 1 | 0 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 3.17 | 1 | 0 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 3.17 | 1 | 0 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 3.44 | 2 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 3.17 | 1 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 2.21 | 1 | 0 |
Glial Cell Tumors [description not available] | 0 | 2.21 | 1 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 2.21 | 1 | 0 |
Glioblastoma A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. | 0 | 2.21 | 1 | 0 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 2.21 | 1 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 2.31 | 1 | 0 |
Mucopolysaccharidoses Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. | 0 | 2.31 | 1 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 2.17 | 1 | 0 |
Innate Inflammatory Response [description not available] | 0 | 2.17 | 1 | 0 |
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 | 2.17 | 1 | 0 |
Bessel-Hagen Disease [description not available] | 0 | 2.52 | 2 | 0 |
Aberrant Tissue [description not available] | 0 | 2.08 | 1 | 0 |
HIV Coinfection [description not available] | 0 | 2.05 | 1 | 0 |
HIV Infections Includes the spectrum of human immunodeficiency virus infections that range from asymptomatic seropositivity, thru AIDS-related complex (ARC), to acquired immunodeficiency syndrome (AIDS). | 0 | 2.05 | 1 | 0 |
Allergic Reaction [description not available] | 0 | 1.93 | 1 | 0 |
Diseases of Immune System [description not available] | 0 | 1.93 | 1 | 0 |
Dermatoses [description not available] | 0 | 1.93 | 1 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 1.93 | 1 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 1.93 | 1 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 1.93 | 1 | 0 |
Allergy, Drug [description not available] | 0 | 2.36 | 2 | 0 |
Granulomas [description not available] | 0 | 2.37 | 2 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 2.36 | 2 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 2.36 | 2 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 2.37 | 2 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 1.96 | 1 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 1.96 | 1 | 0 |
Arthus Phenomenon [description not available] | 0 | 1.95 | 1 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 1.97 | 1 | 0 |
Autoimmune Diabetes [description not available] | 0 | 1.97 | 1 | 0 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 1.97 | 1 | 0 |