| Condition | Indicated | Relationship Strength | Studies | Trials |
|---|
Disease, Pulmonary
[description not available] | 0 | 3.42 | 2 | 0 |
Hemosiderosis
Conditions in which there is a generalized increase in the iron stores of body tissues, particularly of liver and the MONONUCLEAR PHAGOCYTE SYSTEM, without demonstrable tissue damage. The name refers to the presence of stainable iron in the tissue in the form of hemosiderin. | 0 | 3.42 | 2 | 0 |
Lung Diseases
Pathological processes involving any part of the LUNG. | 0 | 3.42 | 2 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial
[description not available] | 0 | 3.68 | 3 | 0 |
Polyarthritis
[description not available] | 0 | 3.04 | 1 | 0 |
Disease Models, Animal
Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 3.35 | 2 | 0 |
Graft-Versus-Host Disease
[description not available] | 0 | 3.04 | 1 | 0 |
Granulomas
[description not available] | 0 | 3.32 | 2 | 0 |
Arthritis
Acute or chronic inflammation of JOINTS. | 0 | 3.04 | 1 | 0 |
Graft vs Host Disease
The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 3.04 | 1 | 0 |
Granuloma
A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 3.32 | 2 | 0 |
Lymphohistiocytosis, Hemophagocytic
A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 3.68 | 3 | 0 |
Macrophage Activation Syndrome
A serious complication of childhood systemic inflammatory disorders that is thought to be caused by excessive activation and proliferation of T-LYMPHOCYTES and MACROPHAGES. It is seen predominantly in children with systemic onset JUVENILE IDIOPATHIC ARTHRITIS. | 0 | 3.04 | 1 | 0 |
Cerebromalacia
[description not available] | 0 | 2.04 | 1 | 0 |
Cryptogenic Infantile Spasms
[description not available] | 0 | 2.43 | 2 | 0 |
Spasms, Infantile
An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8) | 0 | 2.43 | 2 | 0 |
Anasarca
[description not available] | 0 | 2.39 | 2 | 0 |
Innate Inflammatory Response
[description not available] | 0 | 2.38 | 2 | 0 |
Pleurisy
INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 2.02 | 1 | 0 |
Edema
Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 2.39 | 2 | 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 | 2.38 | 2 | 0 |
Sensitivity and Specificity
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 2.03 | 1 | 0 |
Libman-Sacks Disease
[description not available] | 0 | 1.99 | 1 | 0 |
Lupus Erythematosus, Systemic
A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. | 0 | 1.99 | 1 | 0 |
Arterial Obstructive Diseases
[description not available] | 0 | 4.35 | 2 | 2 |
Cancer of Liver
[description not available] | 0 | 4.35 | 2 | 2 |
Colorectal Cancer
[description not available] | 0 | 4.35 | 2 | 2 |
Arterial Occlusive Diseases
Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 4.35 | 2 | 2 |
Liver Neoplasms
Tumors or cancer of the LIVER. | 0 | 4.35 | 2 | 2 |
Colorectal Neoplasms
Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. | 0 | 4.35 | 2 | 2 |
Adjuvant Arthritis
[description not available] | 0 | 1.96 | 1 | 0 |
Rheumatoid Arthritis
[description not available] | 0 | 3.35 | 1 | 1 |
Arthritis, Rheumatoid
A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 3.35 | 1 | 1 |