Condition | Indicated | Relationship Strength | Studies | Trials |
Aldosteronism [description not available] | 0 | 5.77 | 8 | 1 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 5.77 | 8 | 1 |
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 | 3.8 | 2 | 1 |
Adenoma, Basal Cell [description not available] | 0 | 3.07 | 5 | 0 |
Cushing's Syndrome [description not available] | 0 | 4.49 | 9 | 0 |
Adrenal Cortex Cancer [description not available] | 0 | 3.22 | 6 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 3.07 | 5 | 0 |
Adrenal Cortex Neoplasms Tumors or cancers of the ADRENAL CORTEX. | 0 | 3.22 | 6 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 4.49 | 9 | 0 |
Cancer of Liver [description not available] | 0 | 1.96 | 1 | 0 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 1.96 | 1 | 0 |
Congenital Adrenal Hyperplasia [description not available] | 0 | 2.37 | 2 | 0 |
Adrenal Hyperplasia, Congenital A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders. | 0 | 2.37 | 2 | 0 |
Adrenal Cancer [description not available] | 0 | 3.99 | 5 | 0 |
Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. | 0 | 2.38 | 2 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 3.98 | 5 | 0 |
Aldosteronism with Hyperplasia of the Adrenal Cortex [description not available] | 0 | 1.96 | 1 | 0 |
Blood Pressure, High [description not available] | 0 | 1.95 | 1 | 0 |
Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. | 0 | 1.95 | 1 | 0 |
Adenoma, Adrenal Cortical [description not available] | 0 | 2.01 | 1 | 0 |
Gangliocytoma [description not available] | 0 | 1.98 | 1 | 0 |
Cancer of Pituitary [description not available] | 0 | 1.98 | 1 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 1.98 | 1 | 0 |
Adenomatosis, Familial Endocrine [description not available] | 0 | 1.98 | 1 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 1.98 | 1 | 0 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 1.98 | 1 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 1.96 | 1 | 0 |
Pheochromocytoma A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) | 0 | 1.96 | 1 | 0 |
Adrenal Cortex Diseases Pathological processes of the ADRENAL CORTEX. | 0 | 1.96 | 1 | 0 |