Condition | Indicated | Relationship Strength | Studies | Trials |
Libman-Sacks Disease [description not available] | 0 | 2.08 | 1 | 0 |
Enlarged Spleen [description not available] | 0 | 2.08 | 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 | 2.08 | 1 | 0 |
Pyrexia [description not available] | 0 | 4.39 | 1 | 1 |
Acute Promyelocytic Leukemia [description not available] | 0 | 6.41 | 8 | 2 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 4.39 | 1 | 1 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 6.41 | 8 | 2 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 2.13 | 1 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 2.13 | 1 | 0 |
Leukemia, Myeloid, Acute Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES. | 0 | 2.13 | 1 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 2.15 | 1 | 0 |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS. | 0 | 2.15 | 1 | 0 |
Recrudescence [description not available] | 0 | 2.01 | 1 | 0 |
Chromosomal Translocation [description not available] | 0 | 2.01 | 1 | 0 |
Liver Steatosis [description not available] | 0 | 2.03 | 1 | 0 |
Cirrhosis [description not available] | 0 | 2.03 | 1 | 0 |
Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TRIGLYCERIDES, either as a single large droplet or multiple small droplets. Fatty liver is caused by an imbalance in the metabolism of FATTY ACIDS. | 0 | 2.03 | 1 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 2.03 | 1 | 0 |