Condition | Indicated | Relationship Strength | Studies | Trials |
Actinic Keratosis [description not available] | 0 | 3.64 | 1 | 1 |
Keratosis, Actinic White or pink lesions on the arms, hands, face, or scalp that arise from sun-induced DNA DAMAGE to KERATINOCYTES in exposed areas. They are considered precursor lesions to superficial SQUAMOUS CELL CARCINOMA. | 0 | 3.64 | 1 | 1 |
Acanthosis Nigricans A circumscribed melanosis consisting of a brown-pigmented, velvety verrucosity or fine papillomatosis appearing in the axillae and other body folds. It occurs in association with endocrine disorders, underlying malignancy, administration of certain drugs, or as in inherited disorder. | 0 | 2.25 | 1 | 0 |
Canine Diseases [description not available] | 0 | 2.46 | 2 | 0 |
Cancer of Lung [description not available] | 0 | 2.97 | 4 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 2.97 | 4 | 0 |
Breast Cancer [description not available] | 0 | 2.66 | 2 | 0 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 2.66 | 2 | 0 |
Palmoplantaris Pustulosis [description not available] | 0 | 13.53 | 65 | 25 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 13.53 | 65 | 25 |
Metastase [description not available] | 0 | 2.17 | 1 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 2.55 | 2 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 2.78 | 3 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 2.17 | 1 | 0 |
Acantholytic Dyskeratotic Epidermal Nevi [description not available] | 0 | 2.76 | 3 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 2.17 | 1 | 0 |
Carcinoma, Non-Small-Cell Lung A heterogeneous aggregate of at least three distinct histological types of lung cancer, including SQUAMOUS CELL CARCINOMA; ADENOCARCINOMA; and LARGE CELL CARCINOMA. They are dealt with collectively because of their shared treatment strategy. | 0 | 2.17 | 1 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 2.17 | 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 | 2.17 | 1 | 0 |
Keratosis Seborrheica [description not available] | 0 | 2.17 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.17 | 1 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 4.33 | 4 | 1 |
Keratosis Any horny growth such as a wart or callus. | 0 | 4.33 | 4 | 1 |
Keratosis, Seborrheic Benign eccrine poromas that present as multiple oval, brown-to-black plaques, located mostly on the chest and back. The age of onset is usually in the fourth or fifth decade. | 0 | 2.17 | 1 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 2.17 | 1 | 0 |
Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. | 0 | 2.17 | 1 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 2.42 | 2 | 0 |
Benign Chronic Pemphigus [description not available] | 0 | 3.67 | 3 | 0 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 2.42 | 2 | 0 |
Colorectal Cancer [description not available] | 0 | 2.21 | 1 | 0 |
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 | 2.21 | 1 | 0 |
Alopecia Circumscripta [description not available] | 0 | 2.21 | 1 | 0 |
Alopecia Mucinosa [description not available] | 0 | 2.21 | 1 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 2.21 | 1 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 2.08 | 1 | 0 |
Neurofibromatosis 1 An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS). | 0 | 2.08 | 1 | 0 |
Cancer of Colon [description not available] | 0 | 2.98 | 4 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 2.98 | 4 | 0 |
Benign Neoplasms [description not available] | 0 | 3.01 | 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 | 3.01 | 1 | 0 |
Sinus Infections [description not available] | 0 | 2.77 | 3 | 0 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 3.16 | 5 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 2.77 | 3 | 0 |
Hyperactivity, Motor [description not available] | 0 | 2.13 | 1 | 0 |
Agitation, Psychomotor [description not available] | 0 | 2.13 | 1 | 0 |
Psychomotor Agitation A feeling of restlessness associated with increased motor activity. This may occur as a manifestation of nervous system drug toxicity or other conditions. | 0 | 2.13 | 1 | 0 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 7.6 | 7 | 5 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 5.08 | 3 | 1 |
Invasiveness, Neoplasm [description not available] | 0 | 2.04 | 1 | 0 |
Bullous Dermatoses [description not available] | 0 | 2.42 | 2 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 3.83 | 2 | 1 |
Nasal Catarrh [description not available] | 0 | 2.46 | 2 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 2.46 | 2 | 0 |
Contact Dermatitis [description not available] | 0 | 2.05 | 1 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 3.25 | 6 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 2.05 | 1 | 0 |
Disseminated Superficial Actinic Porokeratosis [description not available] | 0 | 2.73 | 3 | 0 |
Porokeratosis A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis. | 0 | 2.73 | 3 | 0 |
Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues. | 0 | 2.06 | 1 | 0 |
Dermatosclerosis [description not available] | 0 | 2.05 | 1 | 0 |
Scleroderma, Localized A term used to describe a variety of localized asymmetrical SKIN thickening that is similar to those of SYSTEMIC SCLERODERMA but without the disease features in the multiple internal organs and BLOOD VESSELS. Lesions may be characterized as patches or plaques (morphea), bands (linear), or nodules. | 0 | 2.05 | 1 | 0 |
Itching [description not available] | 0 | 5.66 | 2 | 1 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 5.66 | 2 | 1 |
Leucocythaemia [description not available] | 0 | 2.07 | 1 | 0 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 2.07 | 1 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 3.25 | 6 | 0 |
Bullous Congenital Ichthyosiform Erythroderma [description not available] | 0 | 2.07 | 1 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 3.25 | 6 | 0 |
Chloasma [description not available] | 0 | 2.07 | 1 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 2.07 | 1 | 0 |
Experimental Neoplasms [description not available] | 0 | 2.08 | 1 | 0 |
Chronic Illness [description not available] | 0 | 5.23 | 4 | 3 |
Licheniform Eruptions [description not available] | 0 | 2.01 | 1 | 0 |
Central Hypothyroidism [description not available] | 0 | 2.01 | 1 | 0 |
Skin Diseases, Vascular Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. | 0 | 2.01 | 1 | 0 |
Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 5.23 | 4 | 3 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 2.01 | 1 | 0 |
Genetic Predisposition [description not available] | 0 | 2.01 | 1 | 0 |
Epidermodysplasia Verruciformis An autosomal recessive trait with impaired cell-mediated immunity. About 15 human papillomaviruses are implicated in associated infection, four of which lead to skin neoplasms. The disease begins in childhood with red papules and later spreads over the body as gray or yellow scales. | 0 | 2.01 | 1 | 0 |
Mole, Skin [description not available] | 0 | 2.7 | 3 | 0 |
Cancer of Skin [description not available] | 0 | 2.92 | 4 | 0 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 2.92 | 4 | 0 |
Ache [description not available] | 0 | 3.84 | 1 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 6.48 | 3 | 2 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 3.84 | 1 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 2.7 | 3 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 2.01 | 1 | 0 |
Blood Pressure, High [description not available] | 0 | 2.01 | 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 | 2.01 | 1 | 0 |
Scalp Dermatoses Skin diseases involving the SCALP. | 0 | 3.4 | 1 | 1 |
Innate Inflammatory Response [description not available] | 0 | 5.77 | 4 | 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 | 5.77 | 4 | 2 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 2.02 | 1 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 2.02 | 1 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 2.02 | 1 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 2.69 | 3 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 2.02 | 1 | 0 |
Calcification, Pathologic [description not available] | 0 | 2.41 | 2 | 0 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 2.02 | 1 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 2.41 | 2 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 2.02 | 1 | 0 |
Absence Seizure [description not available] | 0 | 2.02 | 1 | 0 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 2.02 | 1 | 0 |
Pityriasis Rosea A mild exanthematous inflammation of unknown etiology. It is characterized by the presence of salmon-colored maculopapular lesions. The most striking feature is the arrangement of the lesions such that the long axis is parallel to the lines of cleavage. The eruptions are usually generalized, affecting chiefly the trunk, and the course is often self-limiting. | 0 | 2.02 | 1 | 0 |
Dermatoses [description not available] | 0 | 2.94 | 1 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 2.94 | 1 | 0 |
Acute Necrotizing Pancreatitis [description not available] | 0 | 2.03 | 1 | 0 |
Hyperkeratosis Palmaris et Plantaris [description not available] | 0 | 2.03 | 1 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 2.04 | 1 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 2.03 | 1 | 0 |
Cancer of Head [description not available] | 0 | 2.03 | 1 | 0 |
Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 2.03 | 1 | 0 |
Head and Neck Neoplasms Soft tissue tumors or cancer arising from the mucosal surfaces of the LIP; oral cavity; PHARYNX; LARYNX; and cervical esophagus. Other sites included are the NOSE and PARANASAL SINUSES; SALIVARY GLANDS; THYROID GLAND and PARATHYROID GLANDS; and MELANOMA and non-melanoma skin cancers of the head and neck. (from Holland et al., Cancer Medicine, 4th ed, p1651) | 0 | 2.03 | 1 | 0 |
Experimental Leukemia [description not available] | 0 | 2.37 | 2 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 2.65 | 3 | 0 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 2.65 | 3 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 1.96 | 1 | 0 |
Rachitis [description not available] | 0 | 1.96 | 1 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 2.39 | 2 | 0 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 2.39 | 2 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 2.38 | 2 | 0 |
Osteosarcoma A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed) | 0 | 2.38 | 2 | 0 |
Dermatitis, Irritant A non-allergic contact dermatitis caused by prolonged exposure to irritants and not explained by delayed hypersensitivity mechanisms. | 0 | 1.99 | 1 | 0 |
Diabetic Feet [description not available] | 0 | 1.99 | 1 | 0 |
Fasciitis, Necrotizing A fulminating bacterial infection of the deep layers of the skin and FASCIA. It can be caused by many different organisms, with STREPTOCOCCUS PYOGENES being the most common. | 0 | 1.99 | 1 | 0 |
Verruca [description not available] | 0 | 1.99 | 1 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 1.99 | 1 | 0 |
Diabetic Foot Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION. | 0 | 1.99 | 1 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 1.99 | 1 | 0 |
Parakeratosis Persistence of the nuclei of the keratinocytes into the stratum corneum of the skin. This is a normal state only in the epithelium of true mucous membranes in the mouth and vagina. (Dorland, 27th ed) | 0 | 1.99 | 1 | 0 |
Xeroderma [description not available] | 0 | 3.39 | 1 | 1 |
Ichthyosis Simplex [description not available] | 0 | 3.39 | 1 | 1 |
Ichthyosis, Sex-Linked [description not available] | 0 | 3.39 | 1 | 1 |
Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. | 0 | 3.39 | 1 | 1 |
Granulocytic Leukemia [description not available] | 0 | 2.39 | 2 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 2.39 | 2 | 0 |
Leg Dermatoses A nonspecific term used to denote any cutaneous lesion or group of lesions, or eruptions of any type on the leg. (From Stedman, 25th ed) | 0 | 2 | 1 | 0 |
Acantholysis Bullosa [description not available] | 0 | 2.01 | 1 | 0 |
Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. | 0 | 2.01 | 1 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 2.41 | 2 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 2.41 | 2 | 0 |
Bone Loss, Osteoclastic [description not available] | 0 | 2.66 | 3 | 0 |
Labor, Premature [description not available] | 0 | 1.98 | 1 | 0 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 1.98 | 1 | 0 |
Chronic Kidney Failure [description not available] | 0 | 2.38 | 2 | 0 |
Kidney Failure, Chronic The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION. | 0 | 2.38 | 2 | 0 |
Deficiency, Magnesium [description not available] | 0 | 1.98 | 1 | 0 |
Magnesium Deficiency A nutritional condition produced by a deficiency of magnesium in the diet, characterized by anorexia, nausea, vomiting, lethargy, and weakness. Symptoms are paresthesias, muscle cramps, irritability, decreased attention span, and mental confusion, possibly requiring months to appear. Deficiency of body magnesium can exist even when serum values are normal. In addition, magnesium deficiency may be organ-selective, since certain tissues become deficient before others. (Harrison's Principles of Internal Medicine, 12th ed, p1936) | 0 | 1.98 | 1 | 0 |
Endotoxin Shock [description not available] | 0 | 1.97 | 1 | 0 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 1.97 | 1 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 1.96 | 1 | 0 |
Ectopic Hormone Syndromes [description not available] | 0 | 1.96 | 1 | 0 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 1.96 | 1 | 0 |
Autoimmune Disease [description not available] | 0 | 1.96 | 1 | 0 |
Autoimmune Diseases Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides. | 0 | 1.96 | 1 | 0 |