Condition | Indicated | Relationship Strength | Studies | Trials |
Plasmodium falciparum Malaria [description not available] | 0 | 2.1 | 1 | 0 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 2.1 | 1 | 0 |
Anemia, Fanconi [description not available] | 0 | 2.13 | 1 | 0 |
Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004) | 0 | 2.13 | 1 | 0 |
Contact Dermatitis [description not available] | 0 | 2.21 | 1 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 10.19 | 126 | 1 |
Itching [description not available] | 0 | 4.11 | 3 | 1 |
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 | 2.21 | 1 | 0 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 4.11 | 3 | 1 |
Congenital Zika Syndrome [description not available] | 0 | 2.25 | 1 | 0 |
Zika Virus Infection A viral disease transmitted by the bite of AEDES mosquitoes infected with ZIKA VIRUS. Its mild DENGUE-like symptoms include fever, rash, headaches and ARTHRALGIA. The viral infection during pregnancy, in rare cases, is associated with congenital brain and ocular abnormalities, called Congenital Zika Syndrome, including MICROCEPHALY and may also lead to GUILLAIN-BARRE SYNDROME. | 0 | 2.25 | 1 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 32.41 | 7,908 | 874 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 25.75 | 889 | 239 |
Apnea, Central [description not available] | 0 | 7.67 | 29 | 0 |
Hypoventilation A reduction in the amount of air entering the pulmonary alveoli. | 0 | 14.5 | 92 | 8 |
Sleep Apnea, Central A condition associated with multiple episodes of sleep apnea which are distinguished from obstructive sleep apnea (SLEEP APNEA, OBSTRUCTIVE) by the complete cessation of efforts to breathe. This disorder is associated with dysfunction of central nervous system centers that regulate respiration. | 0 | 7.67 | 29 | 0 |
Bradyarrhythmia [description not available] | 0 | 22.6 | 587 | 99 |
Bradycardia Cardiac arrhythmias that are characterized by excessively slow HEART RATE, usually below 50 beats per minute in human adults. They can be classified broadly into SINOATRIAL NODE dysfunction and ATRIOVENTRICULAR BLOCK. | 0 | 22.6 | 587 | 99 |
Anoxemia [description not available] | 0 | 29.2 | 765 | 69 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 24.2 | 765 | 69 |
Constriction, Pathological [description not available] | 0 | 3.59 | 9 | 0 |
Acquired Laryngeal Stenosis [description not available] | 0 | 2.93 | 4 | 0 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 18.84 | 299 | 12 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 3.59 | 9 | 0 |
Blood Pressure, Low [description not available] | 0 | 16.79 | 132 | 17 |
Ache [description not available] | 0 | 14.27 | 52 | 9 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 16.79 | 132 | 17 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 14.27 | 52 | 9 |
Cyanosis A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule. | 0 | 12.36 | 138 | 2 |
Blood Pressure, High [description not available] | 0 | 9.93 | 56 | 3 |
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 | 9.93 | 56 | 3 |
Apoplexy [description not available] | 0 | 6.4 | 14 | 1 |
Stroke A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810) | 0 | 11.4 | 14 | 1 |
Complete Trisomy 18 Syndrome [description not available] | 0 | 3.14 | 4 | 0 |
Chronic Illness [description not available] | 0 | 10.37 | 40 | 3 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 7.58 | 23 | 1 |
Anhidrosis [description not available] | 0 | 2.41 | 1 | 0 |
Brachial Paresis [description not available] | 0 | 3.81 | 4 | 0 |
Hydrosyringomyelia [description not available] | 0 | 2.66 | 3 | 0 |
Arnold-Chiari Deformity [description not available] | 0 | 5.57 | 17 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 9.36 | 57 | 3 |
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 | 10.37 | 40 | 3 |
Flushing A transient reddening of the face that may be due to fever, certain drugs, exertion, or stress. | 0 | 4.06 | 5 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 5.25 | 4 | 1 |
Cardiac Failure [description not available] | 0 | 9.77 | 47 | 1 |
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 | 9.77 | 47 | 1 |
Ventricular Dysfunction, Left A condition in which the LEFT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE; MYOCARDIAL INFARCTION; and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the left ventricular wall. | 0 | 5.25 | 4 | 1 |
Disease Exacerbation [description not available] | 0 | 9.04 | 21 | 2 |
Preterm Birth [description not available] | 0 | 10.8 | 35 | 2 |
Infantile Respiratory Distress Syndrome [description not available] | 0 | 17.42 | 168 | 19 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 20.09 | 351 | 12 |
Respiratory Distress Syndrome, Newborn A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause. | 0 | 17.42 | 168 | 19 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 10.8 | 35 | 2 |
Palsy [description not available] | 0 | 7.89 | 46 | 1 |
Obesity A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY). | 0 | 22.38 | 238 | 74 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 12.89 | 46 | 1 |
2019 Novel Coronavirus Disease [description not available] | 0 | 5.33 | 15 | 0 |
Absence Seizure [description not available] | 0 | 12.33 | 238 | 2 |
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 | 12.33 | 238 | 2 |
Multiple System Atrophy Syndrome [description not available] | 0 | 4.6 | 5 | 0 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 16.81 | 191 | 9 |
Long Sleeper Syndrome [description not available] | 0 | 14.33 | 120 | 3 |
Sleep Wake Disorders Abnormal sleep-wake schedule or pattern associated with the CIRCADIAN RHYTHM which affect the length, timing, and/or rigidity of the sleep-wake cycle relative to the day-night cycle. | 0 | 14.33 | 120 | 3 |
Multiple System Atrophy A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92) | 0 | 9.6 | 5 | 0 |
Morbid Obesity [description not available] | 0 | 20.96 | 96 | 24 |
Obesity, Morbid The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2. | 0 | 15.96 | 96 | 24 |
Channelopathies A variety of neuromuscular conditions resulting from MUTATIONS in ION CHANNELS manifesting as episodes of EPILEPSY; HEADACHE DISORDERS; and DYSKINESIAS. | 0 | 2.41 | 1 | 0 |
Aura [description not available] | 0 | 17.72 | 123 | 36 |
Deficiency, Mental [description not available] | 0 | 6.31 | 37 | 0 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 17.72 | 123 | 36 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 6.31 | 37 | 0 |
Canine Diseases [description not available] | 0 | 6.3 | 10 | 4 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 16.42 | 231 | 9 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 16.42 | 231 | 9 |
Bacterial Pneumonia [description not available] | 0 | 2.77 | 3 | 0 |
Bronchiolitis Inflammation of the BRONCHIOLES. | 0 | 8.51 | 31 | 1 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 16.21 | 70 | 7 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 2.77 | 3 | 0 |
Infant, Newborn, Diseases Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. | 0 | 15.03 | 271 | 6 |
Anxiety Neuroses [description not available] | 0 | 3.37 | 2 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 8.94 | 20 | 3 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 3.37 | 2 | 0 |
Suffocation [description not available] | 0 | 16.92 | 59 | 3 |
Panic Attacks [description not available] | 0 | 2.96 | 4 | 0 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 11.92 | 59 | 3 |
Panic Disorder A type of anxiety disorder characterized by unexpected panic attacks that last minutes or, rarely, hours. Panic attacks begin with intense apprehension, fear or terror and, often, a feeling of impending doom. Symptoms experienced during a panic attack include dyspnea or sensations of being smothered; dizziness, loss of balance or faintness; choking sensations; palpitations or accelerated heart rate; shakiness; sweating; nausea or other form of abdominal distress; depersonalization or derealization; paresthesias; hot flashes or chills; chest discomfort or pain; fear of dying and fear of not being in control of oneself or going crazy. Agoraphobia may also develop. Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait. | 0 | 2.96 | 4 | 0 |
Tracheal Stenosis A pathological narrowing of the TRACHEA. | 0 | 5.66 | 19 | 1 |
Brain Dead [description not available] | 0 | 21.16 | 263 | 4 |
Bronchopulmonary Dysplasia A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. | 0 | 19.91 | 127 | 67 |
Neonatal Death The death of a live-born INFANT less than 28 days of age. | 0 | 2.41 | 1 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 4.61 | 10 | 0 |
Bleeding [description not available] | 0 | 5.32 | 22 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 5.32 | 22 | 0 |
Failure to Thrive A condition of substandard growth or diminished capacity to maintain normal function. | 0 | 6.31 | 13 | 0 |
Esophageal Reflux [description not available] | 0 | 15.46 | 147 | 6 |
Emesis [description not available] | 0 | 11.52 | 51 | 5 |
Gastroesophageal Reflux Retrograde flow of gastric juice (GASTRIC ACID) and/or duodenal contents (BILE ACIDS; PANCREATIC JUICE) into the distal ESOPHAGUS, commonly due to incompetence of the LOWER ESOPHAGEAL SPHINCTER. | 0 | 15.46 | 147 | 6 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 16.52 | 51 | 5 |
Hemiplegia, Crossed [description not available] | 0 | 3.6 | 9 | 0 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 3.6 | 9 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 8.33 | 70 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 8.33 | 70 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 10.59 | 57 | 6 |
Daytime Sleepiness [description not available] | 0 | 9.46 | 41 | 1 |
Restless Leg Syndrome [description not available] | 0 | 3.83 | 4 | 0 |
Inadequate Sleep [description not available] | 0 | 6.3 | 5 | 1 |
Excessive Periodic Sleep-Related Leg Movements [description not available] | 0 | 4.36 | 4 | 1 |
Disorders of Excessive Somnolence Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia disorders (e.g., IDIOPATHIC HYPERSOMNOLENCE; NARCOLEPSY; and KLEINE-LEVIN SYNDROME) and secondary hypersomnia disorders where excessive somnolence can be attributed to a known cause (e.g., drug affect, MENTAL DISORDERS, and SLEEP APNEA SYNDROME). (From J Neurol Sci 1998 Jan 8;153(2):192-202; Thorpy, Principles and Practice of Sleep Medicine, 2nd ed, p320) | 0 | 9.46 | 41 | 1 |
Restless Legs Syndrome A disorder characterized by aching or burning sensations in the lower and rarely the upper extremities that occur prior to sleep or may awaken the patient from sleep. | 0 | 3.83 | 4 | 0 |
Patent Foramen Ovale [description not available] | 0 | 2.52 | 2 | 0 |
Bends [description not available] | 0 | 6.61 | 17 | 0 |
Foramen Ovale, Patent A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the two upper chambers of the heart. An isolated patent ovale foramen without other structural heart defects is usually of no hemodynamic significance. | 0 | 2.52 | 2 | 0 |
Nervous System Disorders [description not available] | 0 | 7.96 | 31 | 0 |
Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. | 0 | 7.96 | 31 | 0 |
Acute Ischemic Stroke [description not available] | 0 | 2.82 | 2 | 0 |
Cerebral Ischemia [description not available] | 0 | 12.03 | 13 | 1 |
Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT formed within in a cerebral blood vessel it is a thrombotic stroke. When obstruction is formed elsewhere and moved to block a cerebral blood vessel (see CEREBRAL EMBOLISM) it is referred to as embolic stroke. Wake-up stroke refers to ischemic stroke occurring during sleep while cryptogenic stroke refers to ischemic stroke of unknown origin. | 0 | 2.82 | 2 | 0 |
Brain Ischemia Localized reduction of blood flow to brain tissue due to arterial obstruction or systemic hypoperfusion. This frequently occurs in conjunction with brain hypoxia (HYPOXIA, BRAIN). Prolonged ischemia is associated with BRAIN INFARCTION. | 0 | 7.03 | 13 | 1 |
Injuries, Spinal Cord [description not available] | 0 | 5.25 | 20 | 0 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 5.25 | 20 | 0 |
Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome [description not available] | 0 | 7.49 | 28 | 1 |
Rett Syndrome An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199) | 0 | 7.49 | 28 | 1 |
Atelectasis [description not available] | 0 | 21.61 | 70 | 3 |
Infections, Respiratory Syncytial Virus [description not available] | 0 | 6.51 | 31 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 2.81 | 3 | 0 |
Respiratory Syncytial Virus Infections Pneumovirus infections caused by the RESPIRATORY SYNCYTIAL VIRUSES. Humans and cattle are most affected but infections in goats and sheep have been reported. | 0 | 6.51 | 31 | 0 |
Neurodegenerative Diseases Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures. | 0 | 7.81 | 3 | 0 |
Hyperventilation A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide. | 0 | 12.48 | 160 | 5 |
Hypocapnia Clinical manifestation consisting of a deficiency of carbon dioxide in arterial blood. | 0 | 13.26 | 25 | 5 |
Opiate Overdose Accidental or deliberate use of an OPIOID in excess of normal dosage. It includes overdose for prescription and illicit opioids. | 0 | 2.76 | 2 | 0 |
Drug Overdose Accidental or deliberate use of a medication or street drug in excess of normal dosage. | 0 | 3.26 | 6 | 0 |
Abnormality, Heart [description not available] | 0 | 6.29 | 26 | 0 |
Complex Single Ventricle [description not available] | 0 | 2.6 | 1 | 0 |
Heart Defects, Congenital Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. | 0 | 6.29 | 26 | 0 |
Bartholin-Patau Syndrome [description not available] | 0 | 2.31 | 1 | 0 |
Cardiac Death [description not available] | 0 | 5.52 | 26 | 0 |
Cardiac Arrest, Sudden [description not available] | 0 | 3.19 | 5 | 0 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 3.19 | 5 | 0 |
Cot Death [description not available] | 0 | 17.36 | 401 | 5 |
Convulsive Generalized Seizure Disorder [description not available] | 0 | 3.54 | 8 | 0 |
Sudden Unexpected Death in Epilepsy Sudden death in a patient with EPILEPSY associated with SEIZURES and seizure-related symptoms (e.g., APNEA; HYPOXEMIA) without other identifiable accidental causes (e.g., DROWNING; WOUNDS AND INJURIES). | 0 | 8.97 | 9 | 0 |
Psychophysiologic Disorders A group of disorders characterized by physical symptoms that are affected by emotional factors and involve a single organ system, usually under AUTONOMIC NERVOUS SYSTEM control. (American Psychiatric Glossary, 1988) | 0 | 6.6 | 12 | 1 |
Inguinal Hernia [description not available] | 0 | 10.45 | 47 | 9 |
Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults. | 0 | 10.45 | 47 | 9 |
Drug Refractory Epilepsy [description not available] | 0 | 3.11 | 4 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 8.5 | 54 | 0 |
Addiction, Opioid [description not available] | 0 | 6.25 | 5 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 4.58 | 10 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 6.25 | 5 | 0 |
Substance Withdrawal Syndrome Physiological and psychological symptoms associated with withdrawal from the use of a drug after prolonged administration or habituation. The concept includes withdrawal from smoking or drinking, as well as withdrawal from an administered drug. | 0 | 4.58 | 10 | 0 |
Electrocardiogram QT Prolonged [description not available] | 0 | 4.18 | 3 | 0 |
Long QT Syndrome A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME. | 0 | 4.18 | 3 | 0 |
Precordial Catch [description not available] | 0 | 2.76 | 3 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 2.76 | 3 | 0 |
Craniocerebral Injuries [description not available] | 0 | 6.13 | 17 | 0 |
Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be classified by whether or not the skull is penetrated (i.e., penetrating vs. nonpenetrating) or whether there is an associated hemorrhage. | 0 | 6.13 | 17 | 0 |
Amnionitis [description not available] | 0 | 4.06 | 11 | 0 |
Innate Inflammatory Response [description not available] | 0 | 8.61 | 16 | 1 |
Chorioamnionitis INFLAMMATION of the placental membranes (CHORION; AMNION) and connected tissues such as fetal BLOOD VESSELS and UMBILICAL CORD. It is often associated with intrauterine ascending infections during PREGNANCY. | 0 | 4.06 | 11 | 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 | 13.61 | 16 | 1 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 7.16 | 10 | 4 |
Fetal Growth Restriction [description not available] | 0 | 3.92 | 12 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 3.92 | 12 | 0 |
Patency of the Ductus Arteriosus [description not available] | 0 | 11.61 | 38 | 2 |
Ductus Arteriosus, Patent A congenital heart defect characterized by the persistent opening of fetal DUCTUS ARTERIOSUS that connects the PULMONARY ARTERY to the descending aorta (AORTA, DESCENDING) allowing unoxygenated blood to bypass the lung and flow to the PLACENTA. Normally, the ductus is closed shortly after birth. | 0 | 11.61 | 38 | 2 |
Atrioventricular Nodal Reentrant Tachycardia [description not available] | 0 | 2.45 | 2 | 0 |
Consciousness, Loss of [description not available] | 0 | 11.39 | 44 | 8 |
Brain Disorders [description not available] | 0 | 8.7 | 45 | 0 |
Hypermyotonia [description not available] | 0 | 3.28 | 6 | 0 |
Myoclonic Jerk [description not available] | 0 | 8.79 | 14 | 2 |
Hyperekplexia A neurological disorder characterized by an excessive startle reaction with ABNORMAL REFLEX; MYOCLONIC JERKS; and MUSCLE HYPERTONIA. | 0 | 2.72 | 2 | 0 |
Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. | 0 | 8.7 | 45 | 0 |
Gelineau Syndrome [description not available] | 0 | 5.54 | 17 | 0 |
Narcolepsy A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automatic behaviors and AMNESIA. CATAPLEXY; SLEEP PARALYSIS, and hypnagogic HALLUCINATIONS frequently accompany narcolepsy. The pathophysiology of this disorder includes sleep-onset rapid eye movement (REM) sleep, which normally follows stage III or IV sleep. (From Neurology 1998 Feb;50(2 Suppl 1):S2-S7) | 0 | 5.54 | 17 | 0 |
Dysphagia [description not available] | 0 | 15.13 | 43 | 2 |
Deglutition Disorders Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS. | 0 | 10.13 | 43 | 2 |
Auricular Fibrillation [description not available] | 0 | 3.47 | 8 | 0 |
Atrial Fibrillation Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation. | 0 | 3.47 | 8 | 0 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 16.87 | 202 | 8 |
Laryngeal Spasm [description not available] | 0 | 14.41 | 45 | 19 |
Gagging Contraction of the muscle of the PHARYNX caused by stimulation of sensory receptors on the SOFT PALATE, by psychic stimuli, or systemically by drugs. | 0 | 6.67 | 7 | 3 |
Laryngismus A disorder in which the adductor muscles of the VOCAL CORDS exhibit increased activity leading to laryngeal spasm. Laryngismus causes closure of the VOCAL FOLDS and airflow obstruction during inspiration. | 0 | 14.41 | 45 | 19 |
Arrhythmia [description not available] | 0 | 15.48 | 101 | 6 |
Drop Attack [description not available] | 0 | 9.41 | 51 | 1 |
Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in HEART RATE, disorders of electrical impulse generation, or impulse conduction. | 0 | 15.48 | 101 | 6 |
Syncope A transient loss of consciousness and postural tone caused by diminished blood flow to the brain (i.e., BRAIN ISCHEMIA). Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. (From Adams et al., Principles of Neurology, 6th ed, pp367-9) | 0 | 9.41 | 51 | 1 |
Anoxia-Ischemia, Brain [description not available] | 0 | 5.72 | 10 | 2 |
Hypoxia-Ischemia, Brain A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions. | 0 | 5.72 | 10 | 2 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 10.61 | 52 | 3 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 12.27 | 17 | 1 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 10.61 | 52 | 3 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 12.27 | 17 | 1 |
Adverse Drug Event [description not available] | 0 | 3.85 | 4 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 5.07 | 17 | 0 |
Drug-Related Side Effects and Adverse Reactions Disorders that result from the intended use of PHARMACEUTICAL PREPARATIONS. Included in this heading are a broad variety of chemically-induced adverse conditions due to toxicity, DRUG INTERACTIONS, and metabolic effects of pharmaceuticals. | 0 | 3.85 | 4 | 0 |
Snoring Rough, noisy breathing during sleep, due to vibration of the uvula and soft palate. | 0 | 10.73 | 48 | 1 |
Pain, Procedural Pain associated with examination, treatment or procedures. | 0 | 5.69 | 6 | 0 |
Bone Fractures [description not available] | 0 | 5.21 | 4 | 1 |
Cicatrization The formation of fibrous tissue in the place of normal tissue during the process of WOUND HEALING. It includes scar tissue formation occurring in healing internal organs as well as in the skin after surface injuries. | 0 | 3.93 | 2 | 1 |
Injuries, Maxillofacial [description not available] | 0 | 3.99 | 1 | 1 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 3.93 | 2 | 1 |
Fractures, Bone Breaks in bones. | 0 | 5.21 | 4 | 1 |
Lassitude [description not available] | 0 | 4.59 | 10 | 0 |
Chronic Insomnia [description not available] | 0 | 5.43 | 15 | 0 |
Fatigue The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli. | 0 | 4.59 | 10 | 0 |
Sleep Initiation and Maintenance Disorders Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition. | 0 | 5.43 | 15 | 0 |
Abdominal Epilepsy [description not available] | 0 | 4.74 | 11 | 0 |
Epilepsies, Partial Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317) | 0 | 4.74 | 11 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 2.97 | 4 | 0 |
Devic Disease [description not available] | 0 | 2.6 | 1 | 0 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 2.97 | 4 | 0 |
Neuromyelitis Optica A syndrome characterized by acute OPTIC NEURITIS; MYELITIS, TRANSVERSE; demyelinating and/or necrotizing lesions in the OPTIC NERVES and SPINAL CORD; and presence of specific autoantibodies to AQUAPORIN 4. | 0 | 2.6 | 1 | 0 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 5.39 | 7 | 2 |
Breathing Sounds [description not available] | 0 | 11.08 | 53 | 2 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 11.08 | 53 | 2 |
Apnea, Sleep [description not available] | 0 | 17.65 | 167 | 13 |
Sleep Apnea Syndromes Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types. | 0 | 17.65 | 167 | 13 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 2.6 | 1 | 0 |
Cognitive Decline [description not available] | 0 | 2.6 | 1 | 0 |
Infarction, Middle Cerebral Artery NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction. | 0 | 2.6 | 1 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 2.6 | 1 | 0 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 13.4 | 86 | 4 |
Nocturnal Wandering [description not available] | 0 | 3.59 | 3 | 0 |
Anesthesia Related Hyperthermia [description not available] | 0 | 6.24 | 11 | 0 |
Insulin Sensitivity [description not available] | 0 | 4.68 | 3 | 0 |
Insulin Resistance Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS. | 0 | 4.68 | 3 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 2.6 | 1 | 0 |
Atrioventricular Nodal Re-Entrant Tachycardia [description not available] | 0 | 2.97 | 4 | 0 |
Tachycardia, Ventricular An abnormally rapid ventricular rhythm usually in excess of 150 beats per minute. It is generated within the ventricle below the BUNDLE OF HIS, either as autonomic impulse formation or reentrant impulse conduction. Depending on the etiology, onset of ventricular tachycardia can be paroxysmal (sudden) or nonparoxysmal, its wide QRS complexes can be uniform or polymorphic, and the ventricular beating may be independent of the atrial beating (AV dissociation). | 0 | 2.97 | 4 | 0 |
Necrotizing Enterocolitis [description not available] | 0 | 14.98 | 16 | 2 |
Disease, Pulmonary [description not available] | 0 | 10.22 | 46 | 2 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 10.22 | 46 | 2 |
Enterocolitis, Necrotizing ENTEROCOLITIS with extensive ulceration (ULCER) and NECROSIS. It is observed primarily in LOW BIRTH WEIGHT INFANT. | 0 | 9.98 | 16 | 2 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 8.13 | 21 | 1 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 17.51 | 168 | 35 |
Tachypnea Increased RESPIRATORY RATE. | 0 | 6.07 | 9 | 1 |
Breathlessness [description not available] | 0 | 8.36 | 42 | 1 |
Pyrexia [description not available] | 0 | 6.54 | 34 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 13.36 | 42 | 1 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 6.54 | 34 | 0 |
Deafness, Transitory [description not available] | 0 | 3.81 | 2 | 0 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 3.81 | 2 | 0 |
Complication, Postoperative [description not available] | 0 | 16.7 | 198 | 21 |
Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. | 0 | 16.7 | 198 | 21 |
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 | 11.63 | 63 | 3 |
Motor Disorders Motor skills deficits that significantly and persistently interfere with ACTIVITIES OF DAILY LIVING appropriate to chronological age. (from DSM-5) | 0 | 9.67 | 7 | 5 |
Cerebral Palsy, Athetoid [description not available] | 0 | 15.6 | 51 | 41 |
Cerebral Palsy A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7) | 0 | 15.6 | 51 | 41 |
Complications, Infectious Pregnancy [description not available] | 0 | 2.58 | 2 | 0 |
Grippe [description not available] | 0 | 2.8 | 3 | 0 |
Infections, Respiratory [description not available] | 0 | 6.93 | 39 | 0 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 2.8 | 3 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 6.93 | 39 | 0 |
Audiogenic Epilepsy [description not available] | 0 | 2.31 | 1 | 0 |
Epilepsy, Reflex A subtype of epilepsy characterized by seizures that are consistently provoked by a certain specific stimulus. Auditory, visual, and somatosensory stimuli as well as the acts of writing, reading, eating, and decision making are examples of events or activities that may induce seizure activity in affected individuals. (From Neurol Clin 1994 Feb;12(1):57-8) | 0 | 2.31 | 1 | 0 |
Infection [description not available] | 0 | 6.71 | 19 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 6.71 | 19 | 0 |
Glycine Encephalopathy [description not available] | 0 | 2.8 | 3 | 0 |
Absence of Corpus Callosum [description not available] | 0 | 4.19 | 6 | 0 |
Absence Status [description not available] | 0 | 3.39 | 7 | 0 |
Status Epilepticus A prolonged seizure or seizures repeated frequently enough to prevent recovery between episodes occurring over a period of 20-30 minutes. The most common subtype is generalized tonic-clonic status epilepticus, a potentially fatal condition associated with neuronal injury and respiratory and metabolic dysfunction. Nonconvulsive forms include petit mal status and complex partial status, which may manifest as behavioral disturbances. Simple partial status epilepticus consists of persistent motor, sensory, or autonomic seizures that do not impair cognition (see also EPILEPSIA PARTIALIS CONTINUA). Subclinical status epilepticus generally refers to seizures occurring in an unresponsive or comatose individual in the absence of overt signs of seizure activity. (From N Engl J Med 1998 Apr 2;338(14):970-6; Neurologia 1997 Dec;12 Suppl 6:25-30) | 0 | 3.39 | 7 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 4.68 | 6 | 1 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 4.68 | 6 | 1 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 5.57 | 17 | 0 |
Apnea, Obstructive Sleep [description not available] | 0 | 13.89 | 81 | 6 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 13.89 | 81 | 6 |
Equine Diseases [description not available] | 0 | 3.34 | 7 | 0 |
Abnormalities, Respiratory System [description not available] | 0 | 4.3 | 4 | 0 |
Tachyarrhythmia [description not available] | 0 | 8.49 | 41 | 4 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 8.49 | 41 | 4 |
Chondromalacia of Trachea [description not available] | 0 | 2.55 | 2 | 0 |
Sick Sinus Node Syndrome [description not available] | 0 | 2.61 | 2 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 4.33 | 7 | 0 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 9.33 | 7 | 0 |
Botulism, Infantile [description not available] | 0 | 3.1 | 5 | 0 |
Decreased Muscle Tone [description not available] | 0 | 7.88 | 42 | 1 |
Botulism A disease caused by potent protein NEUROTOXINS produced by CLOSTRIDIUM BOTULINUM which interfere with the presynaptic release of ACETYLCHOLINE at the NEUROMUSCULAR JUNCTION. Clinical features include abdominal pain, vomiting, acute PARALYSIS (including respiratory paralysis), blurred vision, and DIPLOPIA. Botulism may be classified into several subtypes (e.g., food-borne, infant, wound, and others). (From Adams et al., Principles of Neurology, 6th ed, p1208) | 0 | 8.1 | 5 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 2.73 | 3 | 0 |
Asystole [description not available] | 0 | 14.24 | 138 | 4 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 14.24 | 138 | 4 |
Aortic Aneurysm, Abdominal An abnormal balloon- or sac-like dilatation in the wall of the ABDOMINAL AORTA which gives rise to the visceral, the parietal, and the terminal (iliac) branches below the aortic hiatus at the diaphragm. | 0 | 2.73 | 3 | 0 |
Bacterial Meningitides [description not available] | 0 | 2.47 | 2 | 0 |
Meningitis, Bacterial Bacterial infections of the leptomeninges and subarachnoid space, frequently involving the cerebral cortex, cranial nerves, cerebral blood vessels, spinal cord, and nerve roots. | 0 | 2.47 | 2 | 0 |
Bordetella pertussis Infection, Respiratory [description not available] | 0 | 7.46 | 29 | 1 |
Whooping Cough A respiratory infection caused by BORDETELLA PERTUSSIS and characterized by paroxysmal coughing ending in a prolonged crowing intake of breath. | 0 | 7.46 | 29 | 1 |
Aspiration, Respiratory [description not available] | 0 | 4.49 | 8 | 0 |
Metabolic Acidosis [description not available] | 0 | 8.96 | 44 | 0 |
Achalasia [description not available] | 0 | 3.74 | 3 | 0 |
Acidosis A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up. | 0 | 8.96 | 44 | 0 |
Esophageal Achalasia A motility disorder of the ESOPHAGUS in which the LOWER ESOPHAGEAL SPHINCTER (near the CARDIA) fails to relax resulting in functional obstruction of the esophagus, and DYSPHAGIA. Achalasia is characterized by a grossly contorted and dilated esophagus (megaesophagus). | 0 | 3.74 | 3 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 8.44 | 35 | 0 |
Deficiency, Protein C [description not available] | 0 | 3.84 | 2 | 1 |
Brain Hemorrhage [description not available] | 0 | 4.46 | 8 | 0 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 2.49 | 2 | 0 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 4.46 | 8 | 0 |
Anoxia, Fetal [description not available] | 0 | 3.36 | 7 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 6.73 | 21 | 1 |
Fetal Hypoxia Deficient oxygenation of FETAL BLOOD. | 0 | 3.36 | 7 | 0 |
Hypovolemic [description not available] | 0 | 2.79 | 3 | 0 |
Hypovolemia An abnormally low volume of blood circulating through the body. It may result in hypovolemic shock (see SHOCK). | 0 | 2.79 | 3 | 0 |
Cancer of the Thyroid [description not available] | 0 | 2.25 | 1 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 2.25 | 1 | 0 |
Hyaline Membrane Disease A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS). | 0 | 7.94 | 35 | 1 |
Hypertrophic Pyloric Stenosis [description not available] | 0 | 8.42 | 2 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 4.66 | 5 | 0 |
Acute Brain Injuries [description not available] | 0 | 8.85 | 40 | 0 |
Anoxia, Brain [description not available] | 0 | 8.09 | 41 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 4.66 | 5 | 0 |
Brain Injuries Acute and chronic (see also BRAIN INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and BRAIN STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits. | 0 | 8.85 | 40 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 2.25 | 1 | 0 |
Group A Strep Infection [description not available] | 0 | 3.23 | 6 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 2.25 | 1 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 3.23 | 6 | 0 |
Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. | 0 | 9.63 | 81 | 0 |
Infections, Coronavirus [description not available] | 0 | 3.45 | 7 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 3.28 | 6 | 0 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 3.45 | 7 | 0 |
Bronchiolitis, Viral An acute inflammatory disease of the lower RESPIRATORY TRACT, caused by paramyxoviruses, occurring primarily in infants and young children; the viruses most commonly implicated are PARAINFLUENZA VIRUS TYPE 3; RESPIRATORY SYNCYTIAL VIRUS, HUMAN; and METAPNEUMOVIRUS. | 0 | 5.51 | 16 | 0 |
Neuromuscular Blockade The intentional interruption of transmission at the NEUROMUSCULAR JUNCTION by external agents, usually neuromuscular blocking agents. It is distinguished from NERVE BLOCK in which nerve conduction (NEURAL CONDUCTION) is interrupted rather than neuromuscular transmission. Neuromuscular blockade is commonly used to produce MUSCLE RELAXATION as an adjunct to anesthesia during surgery and other medical procedures. It is also often used as an experimental manipulation in basic research. It is not strictly speaking anesthesia but is grouped here with anesthetic techniques. The failure of neuromuscular transmission as a result of pathological processes is not included here. | 0 | 19.09 | 120 | 2 |
Concussive Convulsion [description not available] | 0 | 3.61 | 3 | 0 |
Weight Reduction [description not available] | 0 | 6.99 | 6 | 1 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 6.99 | 6 | 1 |
Symptom Cluster [description not available] | 0 | 11.23 | 127 | 0 |
Syndrome A characteristic symptom complex. | 0 | 11.23 | 127 | 0 |
Cranial Nerve X Diseases [description not available] | 0 | 2.51 | 2 | 0 |
Diathesis [description not available] | 0 | 4.49 | 5 | 1 |
Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. | 0 | 8.24 | 47 | 1 |
Ankyloglossia A severe congenital restriction of TONGUE movement, resulting from fusion or adherence of the tongue to the floor of the mouth. In partial ankyloglossia (tongue-tie) the LINGUAL FRENUM is abnormally short, or is attached too close to the tip of the tongue. OMIM: 106280 | 0 | 3.17 | 1 | 0 |
Ranula A form of retention cyst of the floor of the mouth, usually due to obstruction of the ducts of the submaxillary or sublingual glands, presenting a slowly enlarging painless deep burrowing mucocele of one side of the mouth. It is also called sublingual cyst and sublingual ptyalocele. | 0 | 3.17 | 1 | 0 |
Circulatory Collapse [description not available] | 0 | 11.07 | 21 | 0 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 11.07 | 21 | 0 |
Facies The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or the mongoloid facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed) | 0 | 3.14 | 5 | 0 |
Child Mental Disorders [description not available] | 0 | 3.17 | 1 | 0 |
Child Development Deviations [description not available] | 0 | 17.27 | 79 | 46 |
Developmental Disabilities Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed) | 0 | 17.27 | 79 | 46 |
Neurodevelopmental Disorders These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5). | 0 | 3.17 | 1 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 5.61 | 6 | 1 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 5.61 | 6 | 1 |
Brain Swelling [description not available] | 0 | 5.44 | 15 | 0 |
Acquired Encephalocele [description not available] | 0 | 3.17 | 5 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 5.44 | 15 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 6.5 | 12 | 0 |
Cutis Laxa A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed) | 0 | 2.31 | 1 | 0 |
ALTE Apparent Life-Threatening Event [description not available] | 0 | 4.89 | 7 | 1 |
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans [description not available] | 0 | 5.24 | 12 | 0 |
Achondroplasia An autosomal dominant disorder that is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, GENU VARUM, and trident hand. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#100800, April 20, 2001) | 0 | 5.24 | 12 | 0 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 2.31 | 1 | 0 |
Depressive Disorder, Major Disorder in which five (or more) of the following symptoms have been present during the same 2-week period and represent a change from previous functioning; at least one of the symptoms is either (1) depressed mood or (2) loss of interest or pleasure. Symptoms include: depressed mood most of the day, nearly every daily; markedly diminished interest or pleasure in activities most of the day, nearly every day; significant weight loss when not dieting or weight gain; Insomnia or hypersomnia nearly every day; psychomotor agitation or retardation nearly every day; fatigue or loss of energy nearly every day; feelings of worthlessness or excessive or inappropriate guilt; diminished ability to think or concentrate, or indecisiveness, nearly every day; or recurrent thoughts of death, recurrent suicidal ideation without a specific plan, or a suicide attempt. (DSM-5) | 0 | 2.31 | 1 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 2.69 | 3 | 0 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 2.69 | 3 | 0 |
Organophosphorus Poisoning [description not available] | 0 | 3.53 | 8 | 0 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 5.55 | 28 | 0 |
Organophosphate Poisoning Poisoning due to exposure to ORGANOPHOSPHORUS COMPOUNDS, such as ORGANOPHOSPHATES; ORGANOTHIOPHOSPHATES; and ORGANOTHIOPHOSPHONATES. | 0 | 8.53 | 8 | 0 |
Autism Spectrum Disorder Wide continuum of associated cognitive and neurobehavioral disorders, including, but not limited to, three core-defining features: impairments in socialization, impairments in verbal and nonverbal communication, and restricted and repetitive patterns of behaviors. (from DSM-V) | 0 | 2.41 | 1 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 7.48 | 2 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 5.85 | 23 | 0 |
Pneumothorax An accumulation of air or gas in the PLEURAL CAVITY, which may occur spontaneously or as a result of trauma or a pathological process. The gas may also be introduced deliberately during PNEUMOTHORAX, ARTIFICIAL. | 0 | 5.85 | 23 | 0 |
Colorectal Cancer [description not available] | 0 | 3.8 | 1 | 1 |
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 | 3.8 | 1 | 1 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 9.86 | 75 | 4 |
Edema, Pulmonary [description not available] | 0 | 9.18 | 46 | 1 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 9.18 | 46 | 1 |
Cancer of Lung [description not available] | 0 | 4.85 | 13 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 4.85 | 13 | 0 |
Bilateral Headache [description not available] | 0 | 5.48 | 11 | 0 |
Cerebrospinal Fluid Rhinorrhea Discharge of cerebrospinal fluid through the nose. Common etiologies include trauma, neoplasms, and prior surgery, although the condition may occur spontaneously. (Otolaryngol Head Neck Surg 1997 Apr;116(4):442-9) | 0 | 2.31 | 1 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 5.48 | 11 | 0 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 5.32 | 13 | 0 |
Cryptogenic Infantile Spasms [description not available] | 0 | 4.28 | 7 | 0 |
Epilepsy, Temporal Lobe A localization-related (focal) form of epilepsy characterized by recurrent seizures that arise from foci within the TEMPORAL LOBE, most commonly from its mesial aspect. A wide variety of psychic phenomena may be associated, including illusions, hallucinations, dyscognitive states, and affective experiences. The majority of complex partial seizures (see EPILEPSY, COMPLEX PARTIAL) originate from the temporal lobes. Temporal lobe seizures may be classified by etiology as cryptogenic, familial, or symptomatic. (From Adams et al., Principles of Neurology, 6th ed, p321). | 0 | 5.32 | 13 | 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 | 4.28 | 7 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 2.69 | 3 | 0 |
Ependymoma Glioma derived from EPENDYMOGLIAL CELLS that tend to present as malignant intracranial tumors in children and as benign intraspinal neoplasms in adults. It may arise from any level of the ventricular system or central canal of the spinal cord. Intracranial ependymomas most frequently originate in the FOURTH VENTRICLE and histologically are densely cellular tumors which may contain ependymal tubules and perivascular pseudorosettes. Spinal ependymomas are usually benign papillary or myxopapillary tumors. (From DeVita et al., Principles and Practice of Oncology, 5th ed, p2018; Escourolle et al., Manual of Basic Neuropathology, 2nd ed, pp28-9) | 0 | 7.69 | 3 | 0 |
Labor Pain Pain associated with OBSTETRIC LABOR in CHILDBIRTH. It is caused primarily by UTERINE CONTRACTION as well as pressure on the CERVIX; BLADDER; and the GASTROINTESTINAL TRACT. Labor pain mostly occurs in the ABDOMEN; the GROIN; and the BACK. | 0 | 3.69 | 3 | 0 |
Child Behavior Disorders Disturbances considered to be pathological based on age and stage appropriateness, e.g., conduct disturbances and anaclitic depression. This concept does not include psychoneuroses, psychoses, or personality disorders with fixed patterns. | 0 | 9.2 | 11 | 4 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 8.57 | 9 | 0 |
Recrudescence [description not available] | 0 | 13.93 | 96 | 7 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 5.7 | 7 | 1 |
Blood Poisoning [description not available] | 0 | 12.47 | 47 | 12 |
Food Intolerance Digestive system disorder where a particular food irritates the digestive tract or cannot be properly digested (i.e., due to a lack of a digestive enzyme). It differs from FOOD HYPERSENSITIVITY which is an immune system disorder, usually due to specific proteins in food. http://my.clevelandclinic.org/health/articles/problem-foods-is-it-an-allergy-or-intolerance. | 0 | 3.53 | 1 | 1 |
Sepsis Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK. | 0 | 12.47 | 47 | 12 |
Placental Abruption [description not available] | 0 | 3.12 | 5 | 0 |
Abruptio Placentae Premature separation of the normally implanted PLACENTA from the UTERUS. Signs of varying degree of severity include UTERINE BLEEDING, uterine MUSCLE HYPERTONIA, and FETAL DISTRESS or FETAL DEATH. | 0 | 3.12 | 5 | 0 |
Acromegaly Due To Pituitary Adenoma [description not available] | 0 | 2.15 | 1 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 2.91 | 4 | 0 |
Acromegaly A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) | 0 | 2.91 | 4 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 3.37 | 2 | 0 |
Memory Disorders Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions. | 0 | 3.37 | 2 | 0 |
Cyst [description not available] | 0 | 3.78 | 11 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 6.73 | 22 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 5.6 | 28 | 0 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 9.41 | 8 | 0 |
Hallucination of Body Sensation [description not available] | 0 | 3.81 | 4 | 0 |
Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS. | 0 | 3.81 | 4 | 0 |
Concomitant Strabismus [description not available] | 0 | 3.1 | 5 | 0 |
Strabismus Misalignment of the visual axes of the eyes. In comitant strabismus the degree of ocular misalignment does not vary with the direction of gaze. In noncomitant strabismus the degree of misalignment varies depending on direction of gaze or which eye is fixating on the target. (Miller, Walsh & Hoyt's Clinical Neuro-Ophthalmology, 4th ed, p641) | 0 | 3.1 | 5 | 0 |
Action Tremor [description not available] | 0 | 3.06 | 5 | 0 |
Tremor Cyclical movement of a body part that can represent either a physiologic process or a manifestation of disease. Intention or action tremor, a common manifestation of CEREBELLAR DISEASES, is aggravated by movement. In contrast, resting tremor is maximal when there is no attempt at voluntary movement, and occurs as a relatively frequent manifestation of PARKINSON DISEASE. | 0 | 3.06 | 5 | 0 |
Ureteral Calculi Stones in the URETER that are formed in the KIDNEY. They are rarely more than 5 mm in diameter for larger renal stones cannot enter ureters. They are often lodged at the ureteral narrowing and can cause excruciating renal colic. | 0 | 2.69 | 3 | 0 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 10.5 | 16 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 9.07 | 34 | 1 |
Hypocalcemia Reduction of the blood calcium below normal. Manifestations include hyperactive deep tendon reflexes, Chvostek's sign, muscle and abdominal cramps, and carpopedal spasm. (Dorland, 27th ed) | 0 | 9.68 | 11 | 0 |
Hypoglycemia A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH. | 0 | 14.07 | 34 | 1 |
Ape Diseases Diseases of chimpanzees, gorillas, and orangutans. | 0 | 2.17 | 1 | 0 |
Medically Unexplained Symptoms Persistent health symptoms which remain unexplained after a complete medical evaluation. A cluster of symptoms that consistently appear together but without a known cause are referred to as a MEDICALLY UNEXPLAINED SYNDROME (MUS). | 0 | 2.17 | 1 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 2.39 | 2 | 0 |
Sigmoid Colon Diseases [description not available] | 0 | 2.17 | 1 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 2.39 | 2 | 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 | 3.59 | 3 | 0 |
BCECTS [description not available] | 0 | 2.15 | 1 | 0 |
Exercise-Induced Vocal Cord Dysfunction [description not available] | 0 | 2.87 | 3 | 0 |
Complication, Intraoperative [description not available] | 0 | 16.1 | 92 | 49 |
Atresia, Esophageal [description not available] | 0 | 3.93 | 13 | 0 |
Esophageal Atresia Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA. | 0 | 3.93 | 13 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 21.53 | 77 | 68 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 4.26 | 19 | 0 |
Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. | 0 | 9.26 | 19 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 11.73 | 68 | 2 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 10.51 | 15 | 5 |
Distorted Hearing [description not available] | 0 | 4.98 | 3 | 1 |
Day Blindness [description not available] | 0 | 6.14 | 7 | 1 |
Auditory Processing Disorder, Central [description not available] | 0 | 3.53 | 1 | 1 |
Hemorrhage, Retinal [description not available] | 0 | 4.78 | 7 | 0 |
Congenital X-Linked Retinoschisis [description not available] | 0 | 2.17 | 1 | 0 |
Alcohol Abuse [description not available] | 0 | 6.69 | 12 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 2.88 | 4 | 0 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 11.69 | 12 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 2.88 | 4 | 0 |
Retrolental Fibroplasia [description not available] | 0 | 17.32 | 83 | 37 |
Retinopathy of Prematurity A bilateral retinopathy occurring in premature infants treated with excessively high concentrations of oxygen, characterized by vascular dilatation, proliferation, and tortuosity, edema, and retinal detachment, with ultimate conversion of the retina into a fibrous mass that can be seen as a dense retrolental membrane. Usually growth of the eye is arrested and may result in microophthalmia, and blindness may occur. (Dorland, 27th ed) | 0 | 17.32 | 83 | 37 |
Congenital Myasthenia [description not available] | 0 | 10.12 | 10 | 0 |
Myasthenic Syndromes, Congenital A heterogeneous group of disorders characterized by a congenital defect in neuromuscular transmission at the NEUROMUSCULAR JUNCTION. This includes presynaptic, synaptic, and postsynaptic disorders (that are not of autoimmune origin). The majority of these diseases are caused by mutations of various subunits of the nicotinic acetylcholine receptor (RECEPTORS, NICOTINIC) on the postsynaptic surface of the junction. (From Arch Neurol 1999 Feb;56(2):163-7) | 0 | 5.12 | 10 | 0 |
Blast Injuries Injuries resulting when a person is struck by particles impelled with violent force from an explosion. Blast causes pulmonary concussion and hemorrhage, laceration of other thoracic and abdominal viscera, ruptured ear drums, and minor effects in the central nervous system. (From Dorland, 27th ed) | 0 | 3.14 | 5 | 0 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 3.71 | 10 | 0 |
Briquet Syndrome [description not available] | 0 | 3.62 | 3 | 0 |
Somatoform Disorders Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V) | 0 | 3.62 | 3 | 0 |
Genetic Predisposition [description not available] | 0 | 5.31 | 12 | 1 |
Pneumoperitoneum A condition with trapped gas or air in the PERITONEAL CAVITY, usually secondary to perforation of the internal organs such as the LUNG and the GASTROINTESTINAL TRACT, or to recent surgery. Pneumoperitoneum may be purposely introduced to aid radiological examination. | 0 | 7.68 | 3 | 0 |
Emphysema, Subcutaneous [description not available] | 0 | 3.41 | 2 | 0 |
Anemias, Iron-Deficiency [description not available] | 0 | 4.9 | 8 | 1 |
Anemia, Iron-Deficiency Anemia characterized by decreased or absent iron stores, low serum iron concentration, low transferrin saturation, and low hemoglobin concentration or hematocrit value. The erythrocytes are hypochromic and microcytic and the iron binding capacity is increased. | 0 | 4.9 | 8 | 1 |
Aneurysm, Thoracic Aortic [description not available] | 0 | 2.17 | 1 | 0 |
Aneurysm, Aortic [description not available] | 0 | 2.89 | 4 | 0 |
Aortic Dissection [description not available] | 0 | 2.42 | 2 | 0 |
Coin Lesion, Pulmonary [description not available] | 0 | 3.47 | 2 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 2.89 | 4 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 2.17 | 1 | 0 |
Hemoptysis Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES. | 0 | 2.68 | 3 | 0 |
Aortic Aneurysm, Thoracic An abnormal balloon- or sac-like dilatation in the wall of the THORACIC AORTA. This proximal descending portion of aorta gives rise to the visceral and the parietal branches above the aortic hiatus at the diaphragm. | 0 | 2.17 | 1 | 0 |
Aspiration, Meconium [description not available] | 0 | 3.82 | 2 | 0 |
ACD-MPV [description not available] | 0 | 4.6 | 4 | 0 |
Meconium Aspiration Syndrome A condition caused by inhalation of MECONIUM into the LUNG of FETUS or NEWBORN, usually due to vigorous respiratory movements during difficult PARTURITION or respiratory system abnormalities. Meconium aspirate may block small airways leading to difficulties in PULMONARY GAS EXCHANGE and ASPIRATION PNEUMONIA. | 0 | 3.82 | 2 | 0 |
Persistent Fetal Circulation Syndrome A syndrome of persistent PULMONARY HYPERTENSION in the newborn infant (INFANT, NEWBORN) without demonstrable HEART DISEASES. This neonatal condition can be caused by severe pulmonary vasoconstriction (reactive type), hypertrophy of pulmonary arterial muscle (hypertrophic type), or abnormally developed pulmonary arterioles (hypoplastic type). The newborn patient exhibits CYANOSIS and ACIDOSIS due to the persistence of fetal circulatory pattern of right-to-left shunting of blood through a patent ductus arteriosus (DUCTUS ARTERIOSUS, PATENT) and at times a patent foramen ovale (FORAMEN OVALE, PATENT). | 0 | 4.6 | 4 | 0 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 2.73 | 3 | 0 |
Delirium of Mixed Origin [description not available] | 0 | 2.4 | 2 | 0 |
Delirium A disorder characterized by CONFUSION; inattentiveness; disorientation; ILLUSIONS; HALLUCINATIONS; agitation; and in some instances autonomic nervous system overactivity. It may result from toxic/metabolic conditions or structural brain lesions. (From Adams et al., Principles of Neurology, 6th ed, pp411-2) | 0 | 2.4 | 2 | 0 |
Rotavirus Infections Infection with any of the rotaviruses. Specific infections include human infantile diarrhea, neonatal calf diarrhea, and epidemic diarrhea of infant mice. | 0 | 2.74 | 3 | 0 |
Chemical Dependence [description not available] | 0 | 5.93 | 16 | 0 |
Cocaine Abuse [description not available] | 0 | 4.57 | 3 | 0 |
Cannabis Abuse [description not available] | 0 | 4.27 | 2 | 0 |
Marijuana Abuse Use of marijuana associated with abnormal psychological, social, and or occupational functioning. | 0 | 4.27 | 2 | 0 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 5.93 | 16 | 0 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 4.57 | 3 | 0 |
Prodromal Characteristics [description not available] | 0 | 2.21 | 1 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 3.68 | 3 | 0 |
Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) | 0 | 3.68 | 3 | 0 |
Infections, Picornaviridae [description not available] | 0 | 2.81 | 3 | 0 |
Congenital Limb Deformities [description not available] | 0 | 2.21 | 1 | 0 |
Cheyne-Stokes Respiration An abnormal pattern of breathing characterized by alternating periods of apnea and deep, rapid breathing. The cycle begins with slow, shallow breaths that gradually increase in depth and rate and is then followed by a period of apnea. The period of apnea can last 5 to 30 seconds, then the cycle repeats every 45 seconds to 3 minutes. | 0 | 7.92 | 34 | 1 |
Muscular Weakness [description not available] | 0 | 4.17 | 6 | 0 |
Inferior Dislocation [description not available] | 0 | 2.87 | 4 | 0 |
Hypermobility, Joint [description not available] | 0 | 2.17 | 1 | 0 |
Muscle Weakness A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251) | 0 | 4.17 | 6 | 0 |
Segond Fracture [description not available] | 0 | 2.49 | 2 | 0 |
Fractures, Multiple Injuries involving the breaking of either several bones or one bone in two or more places. | 0 | 2.21 | 1 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 2.49 | 2 | 0 |
Diaphragmatic Paralysis [description not available] | 0 | 5.37 | 14 | 0 |
Delayed Awakening from Anesthesia [description not available] | 0 | 3.74 | 3 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 8.11 | 32 | 1 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 13.11 | 32 | 1 |
Alactasia [description not available] | 0 | 3.59 | 1 | 1 |
Lactose Intolerance The condition resulting from the absence or deficiency of LACTASE in the MUCOSA cells of the GASTROINTESTINAL TRACT, and the inability to break down LACTOSE in milk for ABSORPTION. Bacterial fermentation of the unabsorbed lactose leads to symptoms that range from a mild indigestion (DYSPEPSIA) to severe DIARRHEA. Lactose intolerance may be an inborn error or acquired. | 0 | 3.59 | 1 | 1 |
Abnormal Deep Tendon Reflex [description not available] | 0 | 6.25 | 22 | 0 |
Diabetes Insipidus A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst. | 0 | 3.58 | 3 | 0 |
Reflex, Abnormal An abnormal response to a stimulus applied to the sensory components of the nervous system. This may take the form of increased, decreased, or absent reflexes. | 0 | 6.25 | 22 | 0 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 4.41 | 8 | 0 |
Intracranial Hypertension Increased pressure within the cranial vault. This may result from several conditions, including HYDROCEPHALUS; BRAIN EDEMA; intracranial masses; severe systemic HYPERTENSION; PSEUDOTUMOR CEREBRI; and other disorders. | 0 | 4.41 | 8 | 0 |
Aortic Stenosis [description not available] | 0 | 7.66 | 3 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 3.23 | 6 | 0 |
Carditis [description not available] | 0 | 2.91 | 4 | 0 |
Brazilian Spotted Fever [description not available] | 0 | 2.21 | 1 | 0 |
Endotoxin Shock [description not available] | 0 | 3.37 | 7 | 0 |
Afferent Pupillary Defect [description not available] | 0 | 2.21 | 1 | 0 |
Aortic Valve Stenosis A pathological constriction that can occur above (supravalvular stenosis), below (subvalvular stenosis), or at the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA. | 0 | 2.66 | 3 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 2.67 | 3 | 0 |
Cerebral Infarction The formation of an area of NECROSIS in the CEREBRUM caused by an insufficiency of arterial or venous blood flow. Infarcts of the cerebrum are generally classified by hemisphere (i.e., left vs. right), lobe (e.g., frontal lobe infarction), arterial distribution (e.g., INFARCTION, ANTERIOR CEREBRAL ARTERY), and etiology (e.g., embolic infarction). | 0 | 3.23 | 6 | 0 |
Myocarditis Inflammatory processes of the muscular walls of the heart (MYOCARDIUM) which result in injury to the cardiac muscle cells (MYOCYTES, CARDIAC). Manifestations range from subclinical to sudden death (DEATH, SUDDEN). Myocarditis in association with cardiac dysfunction is classified as inflammatory CARDIOMYOPATHY usually caused by INFECTION, autoimmune diseases, or responses to toxic substances. Myocarditis is also a common cause of DILATED CARDIOMYOPATHY and other cardiomyopathies. | 0 | 2.91 | 4 | 0 |
Rocky Mountain Spotted Fever An acute febrile illness caused by RICKETTSIA RICKETTSII. It is transmitted to humans by bites of infected ticks and occurs only in North and South America. Characteristics include a sudden onset with headache and chills and fever lasting about two to three weeks. A cutaneous rash commonly appears on the extremities and trunk about the fourth day of illness. | 0 | 2.21 | 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 | 3.37 | 7 | 0 |
Cardiac Diseases [description not available] | 0 | 5.87 | 17 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 5.87 | 17 | 0 |
Anemia Neonatorum [description not available] | 0 | 6.17 | 5 | 1 |
Anemia, Neonatal The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation. | 0 | 6.17 | 5 | 1 |
Overweight A status with BODY WEIGHT that is above certain standards. In the scale of BODY MASS INDEX, overweight is defined as having a BMI of 25.0-29.9 kg/m2. Overweight may or may not be due to increases in body fat (ADIPOSE TISSUE), hence overweight does not equal over fat. | 0 | 13.37 | 7 | 5 |
Arthritis, Degenerative [description not available] | 0 | 3.77 | 2 | 1 |
Osteoarthritis A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans. | 0 | 3.77 | 2 | 1 |
Hypothermia, Accidental [description not available] | 0 | 7.8 | 30 | 1 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 12.8 | 30 | 1 |
Lethargy A general state of sluggishness, listless, or uninterested, with being tired, and having difficulty concentrating and doing simple tasks. It may be related to DEPRESSION or DRUG ADDICTION. | 0 | 7.61 | 2 | 0 |
Acquired Metabolic Diseases, Brain [description not available] | 0 | 2.5 | 2 | 0 |
Hiccough [description not available] | 0 | 4.62 | 6 | 0 |
Pancreatic Insufficiency [description not available] | 0 | 2.21 | 1 | 0 |
Familial Hyperinsulinemic Hypoglycemia 1 [description not available] | 0 | 2.21 | 1 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 3.98 | 5 | 0 |
Exocrine Pancreatic Insufficiency A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS. | 0 | 2.21 | 1 | 0 |
Congenital Hyperinsulinism A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8). | 0 | 2.21 | 1 | 0 |
Allergy, Milk [description not available] | 0 | 4.81 | 4 | 0 |
Milk Hypersensitivity Allergic reaction to milk (usually cow's milk) or milk products. MILK HYPERSENSITIVITY should be differentiated from LACTOSE INTOLERANCE, an intolerance to milk as a result of congenital deficiency of lactase. | 0 | 4.81 | 4 | 0 |
Cerebral Microangiopathies [description not available] | 0 | 2.21 | 1 | 0 |
Infarct, Lacunar [description not available] | 0 | 2.21 | 1 | 0 |
Cerebral Small Vessel Diseases Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE. | 0 | 2.21 | 1 | 0 |
Sleepiness Compelling urge to sleep. | 0 | 7.21 | 1 | 0 |
Eulenburg Disease [description not available] | 0 | 2.21 | 1 | 0 |
Myotonic Disorders Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. | 0 | 2.21 | 1 | 0 |
Infections, Staphylococcal [description not available] | 0 | 3.63 | 3 | 0 |
Abscess, Retropharyngeal [description not available] | 0 | 3.42 | 2 | 0 |
Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. | 0 | 8.97 | 5 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 3.63 | 3 | 0 |
Adrenal Gland Hypofunction [description not available] | 0 | 2.07 | 1 | 0 |
Hyperphagia Ingestion of a greater than optimal quantity of food. | 0 | 2.07 | 1 | 0 |
Central Hypothyroidism [description not available] | 0 | 3.22 | 6 | 0 |
Adrenal Insufficiency Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. | 0 | 2.07 | 1 | 0 |
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 | 8.22 | 6 | 0 |
Hypokalemia Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed) | 0 | 3.97 | 5 | 0 |
Airway Remodeling The structural changes in the number, mass, size and/or composition of the airway tissues. | 0 | 2.08 | 1 | 0 |
Inadequate Velopharyngeal Closure [description not available] | 0 | 2.08 | 1 | 0 |
A-Thalassemia [description not available] | 0 | 7.08 | 1 | 0 |
Mental Retardation, X-Linked A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS). | 0 | 2.08 | 1 | 0 |
Chondromalacia of Larynx [description not available] | 0 | 2.51 | 2 | 0 |
alpha-Thalassemia A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. | 0 | 7.08 | 1 | 0 |
Laryngomalacia A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the LARYNX. This results in a floppy laryngeal wall making patency difficult to maintain. | 0 | 7.51 | 2 | 0 |
Cardiovascular Stroke [description not available] | 0 | 7.53 | 23 | 1 |
Shock, Cardiogenic Shock resulting from diminution of cardiac output in heart disease. | 0 | 2.95 | 4 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 7.53 | 23 | 1 |
Acidosis, Respiratory Respiratory retention of carbon dioxide. It may be chronic or acute. | 0 | 6.6 | 29 | 2 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 7.58 | 21 | 1 |
ARPKD [description not available] | 0 | 2.08 | 1 | 0 |
Pre-Eclampsia A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. | 0 | 7.58 | 21 | 1 |
Polycystic Kidney, Autosomal Recessive A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY. | 0 | 2.08 | 1 | 0 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 12.49 | 62 | 3 |
Aorticopulmonary Septal Defect [description not available] | 0 | 2.08 | 1 | 0 |
Altered Level of Consciousness [description not available] | 0 | 5.4 | 14 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 5.2 | 8 | 0 |
Acid Aspiration Syndrome [description not available] | 0 | 8.05 | 30 | 1 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 5.2 | 8 | 0 |
Pneumonia, Aspiration A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT. | 0 | 8.05 | 30 | 1 |
Allergy, Drug [description not available] | 0 | 7.16 | 42 | 0 |
Pediculosis [description not available] | 0 | 2.08 | 1 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 7.16 | 42 | 0 |
Lice Infestations Parasitic attack or subsistence on the skin by members of the order Phthiraptera, especially on humans by Pediculus humanus of the family Pediculidae. The hair of the head, eyelashes, and pubis is a frequent site of infestation. (From Dorland, 28th ed; Stedman, 26th ed) | 0 | 2.08 | 1 | 0 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 3.4 | 2 | 0 |
Cancer of Stomach [description not available] | 0 | 2.08 | 1 | 0 |
Dysembryoma [description not available] | 0 | 3.4 | 2 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 3.63 | 3 | 0 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 2.08 | 1 | 0 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 3.4 | 2 | 0 |
Apical Ballooning Syndrome [description not available] | 0 | 3.01 | 1 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 3.3 | 2 | 0 |
Anesthesia Awareness [description not available] | 0 | 3.71 | 3 | 0 |
Takotsubo Cardiomyopathy A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress. | 0 | 3.01 | 1 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 5.56 | 6 | 1 |
Catheter-Associated Infections [description not available] | 0 | 2.49 | 2 | 0 |
Fungemia The presence of fungi circulating in the blood. Opportunistic fungal sepsis is seen most often in immunosuppressed patients with severe neutropenia or in postoperative patients with intravenous catheters and usually follows prolonged antibiotic therapy. | 0 | 2.08 | 1 | 0 |
Candidemia A form of invasive candidiasis where species of CANDIDA are present in the blood. | 0 | 2.08 | 1 | 0 |
Angioma A vascular anomaly due to proliferation of blood or lymphatic vessels that forms a tumor-like mass. Vessels in the angioma may or may not be dilated. | 0 | 2.68 | 3 | 0 |
Cancer of Mouth [description not available] | 0 | 2.08 | 1 | 0 |
Cancer of Skin [description not available] | 0 | 3.13 | 5 | 0 |
Hemangioma A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000) | 0 | 2.68 | 3 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 2.08 | 1 | 0 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 3.13 | 5 | 0 |
Labhart-Willi Syndrome [description not available] | 0 | 3.88 | 4 | 0 |
Prader-Willi Syndrome An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229) | 0 | 8.88 | 4 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 3.27 | 6 | 0 |
Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA. | 0 | 3.3 | 2 | 0 |
Cleft Palate, Isolated [description not available] | 0 | 6.82 | 10 | 1 |
Cancer of Oropharnyx [description not available] | 0 | 3.42 | 2 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 6.82 | 10 | 1 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 3.42 | 2 | 0 |
Cavernous Angioma, Central Nervous System [description not available] | 0 | 2.1 | 1 | 0 |
Hemangioma, Cavernous, Central Nervous System A vascular anomaly composed of a collection of large, thin walled tortuous VEINS that can occur in any part of the central nervous system but lack intervening nervous tissue. Familial occurrence is common and has been associated with a number of genes mapped to 7q, 7p and 3q. Clinical features include SEIZURES; HEADACHE; STROKE; and progressive neurological deficit. | 0 | 2.1 | 1 | 0 |
Harelip [description not available] | 0 | 2.75 | 3 | 0 |
Alobar Holoprosencephaly [description not available] | 0 | 2.08 | 1 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 7.75 | 3 | 0 |
Glossoptosis, Micrognathia, and Cleft Palate [description not available] | 0 | 5.32 | 8 | 0 |
Basedow Disease [description not available] | 0 | 3 | 1 | 0 |
Hyperthyroid [description not available] | 0 | 3 | 1 | 0 |
Complications, Pregnancy [description not available] | 0 | 10.73 | 32 | 2 |
Graves Disease A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMULATING HORMONE RECEPTOR. These autoantibodies activate the TSH receptor, thereby stimulating the THYROID GLAND and hypersecretion of THYROID HORMONES. These autoantibodies can also affect the eyes (GRAVES OPHTHALMOPATHY) and the skin (Graves dermopathy). | 0 | 3 | 1 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 3 | 1 | 0 |
Acute Post-operative Pain [description not available] | 0 | 11.92 | 29 | 12 |
Pain, Postoperative Pain during the period after surgery. | 0 | 11.92 | 29 | 12 |
Cystic Periventricular Leukomalacia [description not available] | 0 | 5.93 | 3 | 1 |
Leukomalacia, Periventricular Degeneration of white matter adjacent to the CEREBRAL VENTRICLES following cerebral hypoxia or BRAIN ISCHEMIA in neonates. The condition primarily affects white matter in the perfusion zone between superficial and deep branches of the MIDDLE CEREBRAL ARTERY. Clinical manifestations include VISION DISORDERS; CEREBRAL PALSY; PARAPLEGIA; SEIZURES; and cognitive disorders. (From Adams et al., Principles of Neurology, 6th ed, p1021; Joynt, Clinical Neurology, 1997, Ch4, pp30-1) | 0 | 5.93 | 3 | 1 |
Acquired Meningomyelocele [description not available] | 0 | 3.49 | 8 | 0 |
Lung Injury, Ventilator-Induced [description not available] | 0 | 3.4 | 2 | 0 |
Cancer of Ovary [description not available] | 0 | 2.08 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 2.89 | 4 | 0 |
Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. | 0 | 2.08 | 1 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 2.89 | 4 | 0 |
Respiratory Syndrome, Acute, Severe [description not available] | 0 | 2.1 | 1 | 0 |
Severe Acute Respiratory Syndrome A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent. | 0 | 2.1 | 1 | 0 |
Blood Loss, Postoperative [description not available] | 0 | 2.7 | 3 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 2.39 | 2 | 0 |
Amaurosis [description not available] | 0 | 9.12 | 10 | 4 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 8.06 | 21 | 1 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 6.31 | 14 | 1 |
Kidney Stones [description not available] | 0 | 2.65 | 3 | 0 |
Labor, Premature [description not available] | 0 | 2.88 | 4 | 0 |
Primary Peritonitis [description not available] | 0 | 2.65 | 3 | 0 |
Embolism, Pulmonary [description not available] | 0 | 3.97 | 14 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 4.31 | 20 | 0 |
Avulsed Tooth [description not available] | 0 | 2.08 | 1 | 0 |
Injuries, Leg [description not available] | 0 | 2.47 | 2 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 9.12 | 10 | 4 |
Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. | 0 | 2.65 | 3 | 0 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 2.65 | 3 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 3.97 | 14 | 0 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 3.82 | 4 | 0 |
Munchausen Syndrome by Proxy A phenomenon in which symptoms of a disease are fabricated by an individual other than the patient causing unnecessary, and often painful, physical examinations and treatments. This syndrome is considered a form of CHILD ABUSE, since another individual, usually a parent, is the source of the fabrication of symptoms and presents the child for medical care. | 0 | 5.52 | 16 | 0 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 3.1 | 5 | 0 |
Cardiac Sinus Arrest [description not available] | 0 | 2.11 | 1 | 0 |
Pallor A clinical manifestation consisting of an unnatural paleness of the skin. | 0 | 4.17 | 6 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 4.52 | 9 | 0 |
Myotonic Dystrophy Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. | 0 | 9.52 | 9 | 0 |
Enterovirus Infections Diseases caused by ENTEROVIRUS. | 0 | 2.94 | 4 | 0 |
Iron Metabolism Disorders Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (From Mosby's Medical, Nursing, & Allied Health Dictionary, 4th ed) | 0 | 2.1 | 1 | 0 |
Dextrocardia A congenital defect in which the heart is located on the right side of the THORAX instead of on the left side (levocardia, the normal position). When dextrocardia is accompanied with inverted HEART ATRIA, a right-sided STOMACH, and a left-sided LIVER, the combination is called dextrocardia with SITUS INVERSUS. Dextrocardia may adversely affect other thoracic organs. | 0 | 2.38 | 2 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 6.73 | 16 | 4 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 2.78 | 3 | 0 |
Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | 0 | 2.1 | 1 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 2.42 | 2 | 0 |
Muscle Disorders [description not available] | 0 | 6.39 | 16 | 1 |
Bone Marrow Failure Syndromes, Congenital [description not available] | 0 | 2.1 | 1 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 6.39 | 16 | 1 |
Mitochondrial Diseases Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | 0 | 2.78 | 3 | 0 |
Co-infection [description not available] | 0 | 2.1 | 1 | 0 |
Developmental Coordination Disorder [description not available] | 0 | 4.4 | 1 | 1 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 3.81 | 4 | 0 |
Icterus Gravis Neonatorum [description not available] | 0 | 6.08 | 21 | 0 |
Jaundice, Neonatal Yellow discoloration of the SKIN; MUCOUS MEMBRANE; and SCLERA in the NEWBORN. It is a sign of NEONATAL HYPERBILIRUBINEMIA. Most cases are transient self-limiting (PHYSIOLOGICAL NEONATAL JAUNDICE) occurring in the first week of life, but some can be a sign of pathological disorders, particularly LIVER DISEASES. | 0 | 6.08 | 21 | 0 |
Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility. | 0 | 3.81 | 4 | 0 |
Laryngitis Inflammation of the LARYNGEAL MUCOSA, including the VOCAL CORDS. Laryngitis is characterized by irritation, edema, and reduced pliability of the mucosa leading to VOICE DISORDERS such as APHONIA and HOARSENESS. | 0 | 2.67 | 3 | 0 |
Regurgitation, Gastric GASTROESOPHAGEAL REFLUX wherein the retrograde flow passes through the UPPER ESOPHAGEAL SPHINCTER | 0 | 2.52 | 2 | 0 |
Laryngopharyngeal Reflux Back flow of gastric contents to the LARYNGOPHARYNX where it comes in contact with tissues of the upper aerodigestive tract. Laryngopharyngeal reflux is an extraesophageal manifestation of GASTROESOPHAGEAL REFLUX. | 0 | 2.52 | 2 | 0 |
Celiac Sprue [description not available] | 0 | 2.1 | 1 | 0 |
Celiac Disease A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. | 0 | 2.1 | 1 | 0 |
Perforated Appendicitis [description not available] | 0 | 2.9 | 4 | 0 |
Femur Neck Fractures [description not available] | 0 | 2.1 | 1 | 0 |
Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 2.9 | 4 | 0 |
Femoral Neck Fractures Fractures of the short, constricted portion of the thigh bone between the femur head and the trochanters. It excludes intertrochanteric fractures which are HIP FRACTURES. | 0 | 2.1 | 1 | 0 |
Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | 0 | 3.28 | 6 | 0 |
Barotrauma Injury following pressure changes; includes injury to the eustachian tube, ear drum, lung and stomach. | 0 | 5.61 | 12 | 0 |
Coronary Thrombosis Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION. | 0 | 2.1 | 1 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 5.2 | 7 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 2.46 | 2 | 0 |
Amyotonia Congenita [description not available] | 0 | 3.07 | 5 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 2.91 | 4 | 0 |
Neuromuscular Diseases A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. | 0 | 3.07 | 5 | 0 |
Direct Hyperbilirubinemia, Neonatal [description not available] | 0 | 5.08 | 3 | 0 |
Bilirubin Encephalopathy [description not available] | 0 | 5.69 | 7 | 0 |
Kernicterus A term used pathologically to describe BILIRUBIN staining of the BASAL GANGLIA; BRAIN STEM; and CEREBELLUM and clinically to describe a syndrome associated with HYPERBILIRUBINEMIA. Clinical features include athetosis, MUSCLE SPASTICITY or hypotonia, impaired vertical gaze, and DEAFNESS. Nonconjugated bilirubin enters the brain and acts as a neurotoxin, often in association with conditions that impair the BLOOD-BRAIN BARRIER (e.g., SEPSIS). This condition occurs primarily in neonates (INFANT, NEWBORN), but may rarely occur in adults. (Menkes, Textbook of Child Neurology, 5th ed, p613) | 0 | 5.69 | 7 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.81 | 3 | 0 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 2.81 | 3 | 0 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 5.68 | 2 | 1 |
Diabetes Mellitus, Type 2 A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY. | 0 | 5.68 | 2 | 1 |
Conus Medullaris Syndrome [description not available] | 0 | 3.22 | 6 | 0 |
Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | 0 | 2.92 | 4 | 0 |
Polysyndactyly [description not available] | 0 | 2.1 | 1 | 0 |
Abnormalities, Urogenital [description not available] | 0 | 2.1 | 1 | 0 |
Abnormalities, Mouth [description not available] | 0 | 2.1 | 1 | 0 |
Lower Extremity Deformities, Congenital Congenital structural abnormalities of the LOWER EXTREMITY. | 0 | 2.1 | 1 | 0 |
CACH Syndrome [description not available] | 0 | 2.49 | 2 | 0 |
Catatonic Rigidity [description not available] | 0 | 4.3 | 7 | 0 |
Muscle Rigidity Continuous involuntary sustained muscle contraction which is often a manifestation of BASAL GANGLIA DISEASES. When an affected muscle is passively stretched, the degree of resistance remains constant regardless of the rate at which the muscle is stretched. This feature helps to distinguish rigidity from MUSCLE SPASTICITY. (From Adams et al., Principles of Neurology, 6th ed, p73) | 0 | 4.3 | 7 | 0 |
Allergic Reaction [description not available] | 0 | 3.81 | 4 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 3.81 | 4 | 0 |
Chronic Lung Injury [description not available] | 0 | 4.61 | 4 | 0 |
Centriacinar Emphysema [description not available] | 0 | 4.94 | 15 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 9.97 | 32 | 4 |
Chromosomal Triplication [description not available] | 0 | 2.48 | 2 | 0 |
Drowning Death that occurs as a result of anoxia or heart arrest, associated with immersion in liquid. | 0 | 11.26 | 20 | 0 |
MODS [description not available] | 0 | 2.48 | 2 | 0 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 2.48 | 2 | 0 |
Asthma, Bronchial [description not available] | 0 | 9.76 | 47 | 2 |
Premature Rupture of Fetal Membranes [description not available] | 0 | 2.11 | 1 | 0 |
Delayed Postpartum Hemorrhage [description not available] | 0 | 4.28 | 4 | 1 |
Bilirubinemia [description not available] | 0 | 3.69 | 10 | 0 |
Diabetes Mellitus, Gestational [description not available] | 0 | 3.36 | 2 | 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 | 9.76 | 47 | 2 |
Fetal Membranes, Premature Rupture Spontaneous tearing of the membranes surrounding the FETUS any time before the onset of OBSTETRIC LABOR. Preterm PROM is membrane rupture before 37 weeks of GESTATION. | 0 | 2.11 | 1 | 0 |
Postpartum Hemorrhage Excess blood loss from uterine bleeding associated with OBSTETRIC LABOR or CHILDBIRTH. It is defined as blood loss greater than 500 ml or of the amount that adversely affects the maternal physiology, such as BLOOD PRESSURE and HEMATOCRIT. Postpartum hemorrhage is divided into two categories, immediate (within first 24 hours after birth) or delayed (after 24 hours postpartum). | 0 | 4.28 | 4 | 1 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 3.39 | 7 | 0 |
Diabetes, Gestational Diabetes mellitus induced by PREGNANCY but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS). Gestational diabetes usually develops in late pregnancy when insulin antagonistic hormones peaks leading to INSULIN RESISTANCE; GLUCOSE INTOLERANCE; and HYPERGLYCEMIA. | 0 | 3.36 | 2 | 0 |
Esophageal Perforation An opening or hole in the ESOPHAGUS that is caused by TRAUMA, injury, or pathological process. | 0 | 2.38 | 2 | 0 |
Cholera Infantum [description not available] | 0 | 3.24 | 6 | 0 |
Experimental Spinal Cord Ischemia [description not available] | 0 | 2.11 | 1 | 0 |
Near Drowning Non-fatal immersion or submersion in water. The subject is resuscitable. | 0 | 4.28 | 7 | 0 |
Alkalosis A pathological condition that removes acid or adds base to the body fluids. | 0 | 9.74 | 12 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 4.41 | 1 | 1 |
Cancer of Colon [description not available] | 0 | 4.74 | 2 | 1 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 4.41 | 1 | 1 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 4.74 | 2 | 1 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 2.43 | 2 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 2.43 | 2 | 0 |
Cerebral Concussion [description not available] | 0 | 3.58 | 9 | 0 |
Closed Head Injuries [description not available] | 0 | 2.43 | 2 | 0 |
Brain Concussion A nonspecific term used to describe transient alterations or loss of consciousness following closed head injuries. The duration of UNCONSCIOUSNESS generally lasts a few seconds, but may persist for several hours. Concussions may be classified as mild, intermediate, and severe. Prolonged periods of unconsciousness (often defined as greater than 6 hours in duration) may be referred to as post-traumatic coma (COMA, POST-HEAD INJURY). (From Rowland, Merritt's Textbook of Neurology, 9th ed, p418) | 0 | 3.58 | 9 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 2.89 | 4 | 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 | 2.89 | 4 | 0 |
Nasal Bleeding [description not available] | 0 | 3.76 | 2 | 1 |
Epistaxis Bleeding from the nose. | 0 | 3.76 | 2 | 1 |
Hyperpotassemia [description not available] | 0 | 5.52 | 6 | 1 |
Hyperkalemia Abnormally high potassium concentration in the blood, most often due to defective renal excretion. It is characterized clinically by electrocardiographic abnormalities (elevated T waves and depressed P waves, and eventually by atrial asystole). In severe cases, weakness and flaccid paralysis may occur. (Dorland, 27th ed) | 0 | 5.52 | 6 | 1 |
Hemorrhagic Shock [description not available] | 0 | 3.22 | 6 | 0 |
Bacterial Disease [description not available] | 0 | 7.71 | 15 | 2 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 7.71 | 15 | 2 |
Fat Necrosis A condition in which the death of adipose tissue results in neutral fats being split into fatty acids and glycerol. | 0 | 2.11 | 1 | 0 |
Cold Panniculitis [description not available] | 0 | 2.11 | 1 | 0 |
Emesis, Postoperative [description not available] | 0 | 9.9 | 9 | 4 |
Postoperative Nausea and Vomiting Emesis and queasiness occurring after anesthesia. | 0 | 9.9 | 9 | 4 |
Pulmonary Hypertension [description not available] | 0 | 5.28 | 21 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 5.28 | 21 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 2.88 | 4 | 0 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 2.88 | 4 | 0 |
Crigler Najjar Syndrome [description not available] | 0 | 2.11 | 1 | 0 |
Idiopathic Hypoparathyroidism A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome. | 0 | 2.13 | 1 | 0 |
Aldosteronism with Hyperplasia of the Adrenal Cortex [description not available] | 0 | 2.53 | 2 | 0 |
Hypoparathyroidism A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone. | 0 | 7.13 | 1 | 0 |
Adolescent Obesity [description not available] | 0 | 2.13 | 1 | 0 |
Viral Diseases [description not available] | 0 | 4.47 | 5 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 4.47 | 5 | 0 |
Neonatal Early-Onset Sepsis [description not available] | 0 | 2.13 | 1 | 0 |
Neonatal Sepsis Blood infection that occurs in an infant younger than 90 days old. Early-onset sepsis is seen in the first week of life and most often appears within 24 hours of birth. Late-onset occurs after 1 week and before 3 months of age. | 0 | 2.13 | 1 | 0 |
Breast Cancer [description not available] | 0 | 7.7 | 3 | 0 |
Neoplasms, Pleural [description not available] | 0 | 2.13 | 1 | 0 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 2.7 | 3 | 0 |
Fasciculation Involuntary contraction of the muscle fibers innervated by a motor unit. Fasciculations may be visualized as a muscle twitch or dimpling under the skin, but usually do not generate sufficient force to move a limb. They may represent a benign condition or occur as a manifestation of MOTOR NEURON DISEASE or PERIPHERAL NERVOUS SYSTEM DISEASES. (Adams et al., Principles of Neurology, 6th ed, p1294) | 0 | 6 | 5 | 2 |
Cystic Kidney Diseases [description not available] | 0 | 2.5 | 2 | 0 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 2.5 | 2 | 0 |
Behavior Disorders [description not available] | 0 | 6.84 | 11 | 1 |
Mental Disorders Psychiatric illness or diseases manifested by breakdowns in the adaptational process expressed primarily as abnormalities of thought, feeling, and behavior producing either distress or impairment of function. | 0 | 6.84 | 11 | 1 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 2.49 | 2 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 2.13 | 1 | 0 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 2.13 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 3.66 | 10 | 0 |
Coronary Disease An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels. | 0 | 3.66 | 10 | 0 |
Transient Tachypnea of Newborn [description not available] | 0 | 3.42 | 2 | 0 |
Esophagotracheal Fistula [description not available] | 0 | 3.57 | 9 | 0 |
Acute Kidney Failure [description not available] | 0 | 4.84 | 8 | 0 |
Chronic Liver Failure [description not available] | 0 | 3.04 | 1 | 0 |
Agitated Emergence [description not available] | 0 | 3.04 | 1 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 3.04 | 1 | 0 |
Acute Kidney Injury Abrupt reduction in kidney function. Acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; ACUTE KIDNEY TUBULAR NECROSIS; and other less severe conditions. | 0 | 4.84 | 8 | 0 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 3.04 | 1 | 0 |
Malnourishment [description not available] | 0 | 2.46 | 2 | 0 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 2.46 | 2 | 0 |
Appetite Disorders [description not available] | 0 | 3.08 | 5 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 4.28 | 7 | 0 |
Basal Ganglia Cerebrovascular Disease A pathological condition caused by impaired blood flow in the basal regions of cerebral hemispheres (BASAL GANGLIA), such as INFARCTION; HEMORRHAGE; or ISCHEMIA in vessels of this brain region including the lateral lenticulostriate arteries. Primary clinical manifestations include involuntary movements (DYSKINESIAS) and muscle weakness (HEMIPARESIS). | 0 | 2.15 | 1 | 0 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 3.08 | 5 | 0 |
Movement Disorders Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions. | 0 | 4.28 | 7 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 2.43 | 2 | 0 |
Tuberous Sclerosis Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. | 0 | 2.43 | 2 | 0 |
Amyoplasia Congenita [description not available] | 0 | 2.13 | 1 | 0 |
Allergy, Wheat [description not available] | 0 | 2.13 | 1 | 0 |
Anaphylactic Reaction [description not available] | 0 | 5.49 | 16 | 0 |
Anaphylaxis An acute hypersensitivity reaction due to exposure to a previously encountered ANTIGEN. The reaction may include rapidly progressing URTICARIA, respiratory distress, vascular collapse, systemic SHOCK, and death. | 0 | 10.49 | 16 | 0 |
Atrial Ectopic Beats [description not available] | 0 | 2.49 | 2 | 0 |
Refractory Depression [description not available] | 0 | 2.15 | 1 | 0 |
Depressive Disorder, Treatment-Resistant Failure to respond to two or more trials of antidepressant monotherapy or failure to respond to four or more trials of different antidepressant therapies. (Campbell's Psychiatric Dictionary, 9th ed.) | 0 | 2.15 | 1 | 0 |
Abdominal Cryptorchidism [description not available] | 0 | 3.12 | 1 | 0 |
Ambiguous Genitalia [description not available] | 0 | 3.12 | 1 | 0 |
Agyria [description not available] | 0 | 3.12 | 1 | 0 |
Disorders of Sex Development In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure to abnormal levels of GONADAL HORMONES in the maternal environment, or disruption of the function of those hormones by ENDOCRINE DISRUPTORS are included. | 0 | 3.12 | 1 | 0 |
Shock, Traumatic Shock produced as a result of trauma. | 0 | 2.65 | 3 | 0 |
Chest Injuries [description not available] | 0 | 2.88 | 4 | 0 |
Blunt Injuries [description not available] | 0 | 2.67 | 3 | 0 |
Happy Puppet Syndrome [description not available] | 0 | 2.04 | 1 | 0 |
Angelman Syndrome A syndrome characterized by multiple abnormalities, MENTAL RETARDATION, and movement disorders. Present usually are skull and other abnormalities, frequent infantile spasms (SPASMS, INFANTILE); easily provoked and prolonged paroxysms of laughter (hence happy); jerky puppetlike movements (hence puppet); continuous tongue protrusion; motor retardation; ATAXIA; MUSCLE HYPOTONIA; and a peculiar facies. It is associated with maternal deletions of chromosome 15q11-13 and other genetic abnormalities. (From Am J Med Genet 1998 Dec 4;80(4):385-90; Hum Mol Genet 1999 Jan;8(1):129-35) | 0 | 2.04 | 1 | 0 |
Blood Clot [description not available] | 0 | 4.44 | 5 | 1 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 4.44 | 5 | 1 |
Convulsions, Grand Mal [description not available] | 0 | 5.38 | 14 | 0 |
Epilepsy, Tonic-Clonic A generalized seizure disorder characterized by recurrent major motor seizures. The initial brief tonic phase is marked by trunk flexion followed by diffuse extension of the trunk and extremities. The clonic phase features rhythmic flexor contractions of the trunk and limbs, pupillary dilation, elevations of blood pressure and pulse, urinary incontinence, and tongue biting. This is followed by a profound state of depressed consciousness (post-ictal state) which gradually improves over minutes to hours. The disorder may be cryptogenic, familial, or symptomatic (caused by an identified disease process). (From Adams et al., Principles of Neurology, 6th ed, p329) | 0 | 5.38 | 14 | 0 |
Pachymeningitis [description not available] | 0 | 4.28 | 7 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 3.48 | 8 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 4.28 | 7 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 3.48 | 8 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 2.44 | 2 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 2.44 | 2 | 0 |
Angor Pectoris [description not available] | 0 | 4.13 | 6 | 0 |
Coronary Vessel Anomalies Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANEURYSM; MYOCARDIAL BRIDGING; and others. | 0 | 2.43 | 2 | 0 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 4.13 | 6 | 0 |
Microcephaly A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) | 0 | 4.02 | 5 | 0 |
Advanced Sleep Phase Syndrome [description not available] | 0 | 2.04 | 1 | 0 |
Sleep Disorders, Circadian Rhythm Dyssomnias associated with disruption of the normal 24 hour sleep wake cycle secondary to travel (e.g., JET LAG SYNDROME), shift work, or other causes. | 0 | 2.04 | 1 | 0 |
Brown Tendon Sheath Syndrome [description not available] | 0 | 4.54 | 9 | 0 |
Chronic Kidney Failure [description not available] | 0 | 5.2 | 7 | 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 | 5.2 | 7 | 0 |
Dirofilariasis Infection with nematodes of the genus DIROFILARIA, usually in animals, especially dogs, but occasionally in man. | 0 | 2.44 | 2 | 0 |
Esophageal Dysmotility [description not available] | 0 | 2.41 | 2 | 0 |
Cranial Airocele [description not available] | 0 | 2.96 | 1 | 0 |
Brain Injuries, Penetrating [description not available] | 0 | 2.04 | 1 | 0 |
Wounds, Gunshot Disruption of structural continuity of the body as a result of the discharge of firearms. | 0 | 2.4 | 2 | 0 |
Central Nervous System Disease [description not available] | 0 | 5.85 | 17 | 0 |
Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | 0 | 5.85 | 17 | 0 |
Aqueductal Stenosis [description not available] | 0 | 4.58 | 26 | 0 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 9.83 | 13 | 0 |
Hangman Fracture [description not available] | 0 | 3.11 | 5 | 0 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 3.11 | 5 | 0 |
Bacteriuria The presence of bacteria in the urine which is normally bacteria-free. These bacteria are from the URINARY TRACT and are not contaminants of the surrounding tissues. Bacteriuria can be symptomatic or asymptomatic. Significant bacteriuria is an indicator of urinary tract infection. | 0 | 2.05 | 1 | 0 |
Bacteremia The presence of viable bacteria circulating in the blood. Fever, chills, tachycardia, and tachypnea are common acute manifestations of bacteremia. The majority of cases are seen in already hospitalized patients, most of whom have underlying diseases or procedures which render their bloodstreams susceptible to invasion. | 0 | 2.94 | 4 | 0 |
Postintubation Croup [description not available] | 0 | 2.05 | 1 | 0 |
Infections, Respirovirus [description not available] | 0 | 4.11 | 16 | 0 |
Croup Inflammation involving the GLOTTIS or VOCAL CORDS and the subglottic larynx. Croup is characterized by a barking cough, HOARSENESS, and persistent inspiratory STRIDOR (a high-pitched breathing sound). It occurs chiefly in infants and children. | 0 | 2.05 | 1 | 0 |
Cardiac Output, Low A state of subnormal or depressed cardiac output at rest or during stress. It is a characteristic of CARDIOVASCULAR DISEASES, including congenital, valvular, rheumatic, hypertensive, coronary, and cardiomyopathic. The serious form of low cardiac output is characterized by marked reduction in STROKE VOLUME, and systemic vasoconstriction resulting in cold, pale, and sometimes cyanotic extremities. | 0 | 4.78 | 4 | 0 |
Food Poisoning [description not available] | 0 | 2.88 | 4 | 0 |
A-V Dissociation [description not available] | 0 | 4.21 | 18 | 0 |
Meningitis, Viral Viral infections of the leptomeninges and subarachnoid space. TOGAVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; RUBELLA; BUNYAVIRIDAE INFECTIONS; ORBIVIRUS infections; PICORNAVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RHABDOVIRIDAE INFECTIONS; ARENAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; JC VIRUS infections; and RETROVIRIDAE INFECTIONS may cause this form of meningitis. Clinical manifestations include fever, headache, neck pain, vomiting, PHOTOPHOBIA, and signs of meningeal irritation. (From Joynt, Clinical Neurology, 1996, Ch26, pp1-3) | 0 | 2.4 | 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 | 2.91 | 4 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Icterus [description not available] | 0 | 3.05 | 5 | 0 |
Sclerema Neonatorum A severe, sometimes fatal, disorder of adipose tissue occurring chiefly in preterm or debilitated infants suffering from an underlying illness and manifested by a diffuse, nonpitting induration of the affected tissue. The skin becomes cold, yellowish, mottled, and inflexible. | 0 | 2.05 | 1 | 0 |
Jaundice A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction. | 0 | 3.05 | 5 | 0 |
Axonal Injury, Diffuse [description not available] | 0 | 2.43 | 2 | 0 |
Abdomen, Acute A clinical syndrome with acute abdominal pain that is severe, localized, and rapid in onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases. | 0 | 2.05 | 1 | 0 |
Epididymitis Inflammation of the EPIDIDYMIS. Its clinical features include enlarged epididymis, a swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related to infections in the URINARY TRACT, which likely spread to the EPIDIDYMIS through either the VAS DEFERENS or the lymphatics of the SPERMATIC CORD. | 0 | 2.05 | 1 | 0 |
Infection, Wound [description not available] | 0 | 2.05 | 1 | 0 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 2.42 | 2 | 0 |
Spermatic Cord Torsion The twisting of the SPERMATIC CORD due to an anatomical abnormality that left the TESTIS mobile and dangling in the SCROTUM. The initial effect of testicular torsion is obstruction of venous return. Depending on the duration and degree of cord rotation, testicular symptoms range from EDEMA to interrupted arterial flow and testicular pain. If blood flow to testis is absent for 4 to 6 h, SPERMATOGENESIS may be permanently lost. | 0 | 2.05 | 1 | 0 |
Rib Fractures Fractures of any of the RIBS. | 0 | 4.51 | 5 | 0 |
Adiadochokinesis [description not available] | 0 | 3.62 | 3 | 0 |
Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) | 0 | 3.62 | 3 | 0 |
Agenesis of Hemidiaphragm [description not available] | 0 | 2.37 | 2 | 0 |
Diaphragmatic Hernia [description not available] | 0 | 3.46 | 8 | 0 |
Hernias, Diaphragmatic, Congenital Protrusion of abdominal structures into the THORAX as a result of embryologic defects in the DIAPHRAGM often present in the neonatal period. It can be isolated, syndromic, non-syndromic or be a part of chromosome abnormality. Associated pulmonary hypoplasia and PULMONARY HYPERTENSION can further complicate stabilization and surgical intervention. | 0 | 2.37 | 2 | 0 |
CBS Deficiency [description not available] | 0 | 2.39 | 2 | 0 |
Homocystinuria Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979) | 0 | 2.39 | 2 | 0 |
Ptosis, Eyelid [description not available] | 0 | 2.05 | 1 | 0 |
Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. | 0 | 2.05 | 1 | 0 |
Bruise [description not available] | 0 | 2.96 | 1 | 0 |
Linear Skull Fracture [description not available] | 0 | 4.63 | 6 | 0 |
Injuries, Neck [description not available] | 0 | 3.6 | 3 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 2.96 | 1 | 0 |
Embryopathies [description not available] | 0 | 5.36 | 14 | 0 |
Neurally Mediated Faint [description not available] | 0 | 4.33 | 4 | 0 |
Hypotension, Postural [description not available] | 0 | 4.37 | 8 | 0 |
Hypotension, Orthostatic A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE. | 0 | 4.37 | 8 | 0 |
Agitation, Psychomotor [description not available] | 0 | 7.98 | 6 | 5 |
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 | 7.98 | 6 | 5 |
Hay Fever [description not available] | 0 | 2.05 | 1 | 0 |
Nasal Catarrh [description not available] | 0 | 2.89 | 4 | 0 |
Rhinitis, Allergic, Nonseasonal [description not available] | 0 | 2.05 | 1 | 0 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 2.05 | 1 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 7.89 | 4 | 0 |
Rhinitis, Allergic, Perennial Inflammation of the mucous membrane of the nose similar to that found in hay fever except that symptoms persist throughout the year. The causes are usually air-borne allergens, particularly dusts, feathers, molds, animal fur, etc. | 0 | 2.05 | 1 | 0 |
Abnormal Movements [description not available] | 0 | 2.43 | 2 | 0 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 3.3 | 2 | 0 |
Benign Infantile Myoclonic Epilepsy [description not available] | 0 | 2.44 | 2 | 0 |
Encephalomyelitis, Subacute Necrotizing [description not available] | 0 | 2.71 | 3 | 0 |
Epilepsies, Myoclonic A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic. | 0 | 2.44 | 2 | 0 |
Leigh Disease A group of metabolic disorders primarily of infancy characterized by the subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, dysphagia, and lactic acidosis. Pathological features include spongy degeneration of the neuropile of the basal ganglia, thalamus, brain stem, and spinal cord. Patterns of inheritance include X-linked recessive, autosomal recessive, and mitochondrial. Leigh disease has been associated with mutations in genes for the PYRUVATE DEHYDROGENASE COMPLEX; CYTOCHROME-C OXIDASE; ATP synthase subunit 6; and subunits of mitochondrial complex I. (From Menkes, Textbook of Child Neurology, 5th ed, p850). | 0 | 2.71 | 3 | 0 |
Lipodystrophy, Intestinal [description not available] | 0 | 2.05 | 1 | 0 |
Benedict Syndrome [description not available] | 0 | 2.43 | 2 | 0 |
Basilar Artery Insufficiency [description not available] | 0 | 2.05 | 1 | 0 |
Dissecting Vertebral Artery Aneurysm [description not available] | 0 | 2.05 | 1 | 0 |
Gastroenteritis INFLAMMATION of any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. Causes of gastroenteritis are many including genetic, infection, HYPERSENSITIVITY, drug effects, and CANCER. | 0 | 2.05 | 1 | 0 |
Complex Partial Epilepsy [description not available] | 0 | 3.35 | 2 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 3.09 | 5 | 0 |
Epilepsy, Complex Partial A disorder characterized by recurrent partial seizures marked by impairment of cognition. During the seizure the individual may experience a wide variety of psychic phenomenon including formed hallucinations, illusions, deja vu, intense emotional feelings, confusion, and spatial disorientation. Focal motor activity, sensory alterations and AUTOMATISM may also occur. Complex partial seizures often originate from foci in one or both temporal lobes. The etiology may be idiopathic (cryptogenic partial complex epilepsy) or occur as a secondary manifestation of a focal cortical lesion (symptomatic partial complex epilepsy). (From Adams et al., Principles of Neurology, 6th ed, pp317-8) | 0 | 3.35 | 2 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 3.08 | 5 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 8.08 | 5 | 0 |
Air Embolism [description not available] | 0 | 4.49 | 9 | 0 |
Dysesthesia [description not available] | 0 | 2.87 | 4 | 0 |
Shaken Baby Syndrome Brain injuries resulted from vigorous shaking of an infant or young child held by the chest, shoulders, or extremities causing extreme cranial acceleration. It is characterized by the intracranial and intraocular hemorrhages with no evident external trauma. Serious cases may result in death. | 0 | 2.44 | 2 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 4.25 | 7 | 0 |
Abdominal Cramps [description not available] | 0 | 4.15 | 6 | 0 |
E coli Infections [description not available] | 0 | 2.89 | 4 | 0 |
Cardiac Hypertrophy Enlargement of the HEART due to chamber HYPERTROPHY, an increase in wall thickness without an increase in the number of cells (MYOCYTES, CARDIAC). It is the result of increase in myocyte size, mitochondrial and myofibrillar mass, as well as changes in extracellular matrix. | 0 | 3.21 | 6 | 0 |
Bacterial Endocarditides [description not available] | 0 | 2.69 | 3 | 0 |
Diaphragmatic Hernia, Traumatic [description not available] | 0 | 2.05 | 1 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 3.37 | 7 | 0 |
Endocarditis, Bacterial Inflammation of the ENDOCARDIUM caused by BACTERIA that entered the bloodstream. The strains of bacteria vary with predisposing factors, such as CONGENITAL HEART DEFECTS; HEART VALVE DISEASES; HEART VALVE PROSTHESIS IMPLANTATION; or intravenous drug use. | 0 | 2.69 | 3 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 2.89 | 4 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 3.21 | 6 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 2.4 | 2 | 0 |
Lung Injury, Acute [description not available] | 0 | 2.05 | 1 | 0 |
Acute Lung Injury A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological). | 0 | 2.05 | 1 | 0 |
Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | 0 | 7.7 | 3 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 3.07 | 5 | 0 |
Anterior Fascicular Block [description not available] | 0 | 3.8 | 4 | 0 |
Carbohydrate Metabolism, Inborn Error [description not available] | 0 | 2.44 | 2 | 0 |
Deficiency of Glucose-6-Phosphate Dehydrogenase [description not available] | 0 | 4.58 | 4 | 0 |
Bronze Diabetes [description not available] | 0 | 2.05 | 1 | 0 |
Elevated Cholesterol [description not available] | 0 | 2.05 | 1 | 0 |
Diseases, Metabolic [description not available] | 0 | 4.95 | 9 | 0 |
Neuroleptic Malignant Syndrome A potentially fatal syndrome associated primarily with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS) which are in turn associated with dopaminergic receptor blockade (see RECEPTORS, DOPAMINE) in the BASAL GANGLIA and HYPOTHALAMUS, and sympathetic dysregulation. Clinical features include diffuse MUSCLE RIGIDITY; TREMOR; high FEVER; diaphoresis; labile blood pressure; cognitive dysfunction; and autonomic disturbances. Serum CPK level elevation and a leukocytosis may also be present. (From Adams et al., Principles of Neurology, 6th ed, p1199; Psychiatr Serv 1998 Sep;49(9):1163-72) | 0 | 7.42 | 2 | 0 |
Porphyria [description not available] | 0 | 2.38 | 2 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 2.05 | 1 | 0 |
Glucosephosphate Dehydrogenase Deficiency A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia. | 0 | 4.58 | 4 | 0 |
Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) | 0 | 2.05 | 1 | 0 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 2.05 | 1 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 4.95 | 9 | 0 |
Porphyrias A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues. | 0 | 2.38 | 2 | 0 |
Conducted Energy Weapon Injuries The injuries caused by conducted energy weapons such as stun guns, shock batons, and cattle prods. | 0 | 2.05 | 1 | 0 |
Female Genital Neoplasms [description not available] | 0 | 2.05 | 1 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 2.05 | 1 | 0 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 2.05 | 1 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 2.05 | 1 | 0 |
Endotoxemia A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators. | 0 | 2.42 | 2 | 0 |
Desmoid [description not available] | 0 | 2.05 | 1 | 0 |
Extrasystole, Ventricular [description not available] | 0 | 2.05 | 1 | 0 |
Cardiac Cancer [description not available] | 0 | 2.38 | 2 | 0 |
Angiomyxoma [description not available] | 0 | 2.38 | 2 | 0 |
Fibromatosis, Aggressive A childhood counterpart of abdominal or extra-abdominal desmoid tumors, characterized by firm subcutaneous nodules that grow rapidly in any part of the body but do not metastasize. The adult form of abdominal fibromatosis is FIBROMATOSIS, ABDOMINAL. (Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Intestinal Volvulus A twisting in the intestine (INTESTINES) that can cause INTESTINAL OBSTRUCTION. | 0 | 2.05 | 1 | 0 |
Neoplasms, Nerve Sheath [description not available] | 0 | 2.05 | 1 | 0 |
Nasal Diseases [description not available] | 0 | 2.05 | 1 | 0 |
Nerve Sheath Neoplasms Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category. | 0 | 2.05 | 1 | 0 |
Ganglion Cysts Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE, especially of the hands, wrists, or feet. They are not true cysts as they lack epithelial wall. They are distinguished from SYNOVIAL CYSTS by the lack of communication with a joint cavity or the SYNOVIAL MEMBRANE. | 0 | 2.06 | 1 | 0 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 8.31 | 14 | 6 |
Out-of-Hospital Cardiac Arrest Occurrence of heart arrest in an individual when there is no immediate access to medical personnel or equipment. | 0 | 2.05 | 1 | 0 |
Inclusion Body Myopathy, Sporadic [description not available] | 0 | 2.05 | 1 | 0 |
AIRE Deficiency [description not available] | 0 | 2.05 | 1 | 0 |
Acidosis, Renal Tubular Type IV [description not available] | 0 | 2.05 | 1 | 0 |
Myositis, Inclusion Body Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10) | 0 | 2.05 | 1 | 0 |
Catatonic Schizophrenia [description not available] | 0 | 2.06 | 1 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 2.06 | 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 | 2.06 | 1 | 0 |
Injuries, Radiation [description not available] | 0 | 2.06 | 1 | 0 |
Aganglionic Megacolon [description not available] | 0 | 3.14 | 5 | 0 |
Hirschsprung Disease Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON. | 0 | 3.14 | 5 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 2.69 | 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 | 2.69 | 3 | 0 |
Convulsions, Febrile [description not available] | 0 | 4.07 | 3 | 0 |
Seizures, Febrile Seizures that occur during a febrile episode. It is a common condition, affecting 2-5% of children aged 3 months to five years. An autosomal dominant pattern of inheritance has been identified in some families. The majority are simple febrile seizures (generally defined as generalized onset, single seizures with a duration of less than 30 minutes). Complex febrile seizures are characterized by focal onset, duration greater than 30 minutes, and/or more than one seizure in a 24 hour period. The likelihood of developing epilepsy (i.e., a nonfebrile seizure disorder) following simple febrile seizures is low. Complex febrile seizures are associated with a moderately increased incidence of epilepsy. (From Menkes, Textbook of Child Neurology, 5th ed, p784) | 0 | 4.07 | 3 | 0 |
Mouth Breathing Abnormal breathing through the mouth, usually associated with obstructive disorders of the nasal passages. | 0 | 4.15 | 6 | 0 |
Constricted Pupil [description not available] | 0 | 2.42 | 2 | 0 |
Decerebrate Posturing [description not available] | 0 | 6.6 | 32 | 0 |
Miosis Pupillary constriction. This may result from congenital absence of the dilatator pupillary muscle, defective sympathetic innervation, or irritation of the CONJUNCTIVA or CORNEA. | 0 | 2.42 | 2 | 0 |
Heritable Pulmonary Arterial Hypertension [description not available] | 0 | 2.06 | 1 | 0 |
Familial Primary Pulmonary Hypertension Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease. | 0 | 2.06 | 1 | 0 |
Cancer of Kidney [description not available] | 0 | 2.37 | 2 | 0 |
Double Nuchal Cord [description not available] | 0 | 2.06 | 1 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 2.37 | 2 | 0 |
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 | 2.43 | 2 | 0 |
Laryngeal Nerve Avulsion [description not available] | 0 | 2.07 | 1 | 0 |
Injuries, Multiple [description not available] | 0 | 2.98 | 1 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 5.74 | 15 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 5.74 | 15 | 0 |
Mydriasis Dilation of pupils to greater than 6 mm combined with failure of the pupils to constrict when stimulated with light. This condition may occur due to injury of the pupillary fibers in the oculomotor nerve, in acute angle-closure glaucoma, and in ADIE SYNDROME. | 0 | 7.96 | 4 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 2.37 | 2 | 0 |
Apple Peel Small Bowel Syndrome [description not available] | 0 | 2.66 | 3 | 0 |
Constipation Infrequent or difficult evacuation of FECES. These symptoms are associated with a variety of causes, including low DIETARY FIBER intake, emotional or nervous disturbances, systemic and structural disorders, drug-induced aggravation, and infections. | 0 | 2.37 | 2 | 0 |
Deaf Mutism [description not available] | 0 | 8.84 | 7 | 4 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 8.84 | 7 | 4 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 2.99 | 1 | 0 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 2.99 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 2.07 | 1 | 0 |
Cirrhosis, Liver [description not available] | 0 | 2.37 | 2 | 0 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 2.37 | 2 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 2.07 | 1 | 0 |
Lock Jaw [description not available] | 0 | 2.41 | 2 | 0 |
Auricular Flutter [description not available] | 0 | 7.65 | 3 | 0 |
Atrial Flutter Rapid, irregular atrial contractions caused by a block of electrical impulse conduction in the right atrium and a reentrant wave front traveling up the inter-atrial septum and down the right atrial free wall or vice versa. Unlike ATRIAL FIBRILLATION which is caused by abnormal impulse generation, typical atrial flutter is caused by abnormal impulse conduction. As in atrial fibrillation, patients with atrial flutter cannot effectively pump blood into the lower chambers of the heart (HEART VENTRICLES). | 0 | 2.65 | 3 | 0 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 2.7 | 3 | 0 |
Bilateral Multicystic Dysplastic Kidneys [description not available] | 0 | 2.07 | 1 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 3.84 | 4 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 5.97 | 5 | 2 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 5.97 | 5 | 2 |
Depth Intoxication [description not available] | 0 | 4.85 | 4 | 0 |
Antidiuretic Hormone, Inappropriate Secretion [description not available] | 0 | 2.4 | 2 | 0 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 3.78 | 11 | 0 |
Inappropriate ADH Syndrome A condition of HYPONATREMIA and renal salt loss attributed to overexpansion of BODY FLUIDS resulting from sustained release of ANTIDIURETIC HORMONES which stimulates renal resorption of water. It is characterized by normal KIDNEY function, high urine OSMOLALITY, low serum osmolality, and neurological dysfunction. Etiologies include ADH-producing neoplasms, injuries or diseases involving the HYPOTHALAMUS, the PITUITARY GLAND, and the LUNG. This syndrome can also be drug-induced. | 0 | 2.4 | 2 | 0 |
Astrocytosis [description not available] | 0 | 2.9 | 4 | 0 |
Methemoglobinemia The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed) | 0 | 3.6 | 3 | 0 |
Benign Neonatal Sleep Myoclonus [description not available] | 0 | 2.99 | 1 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 4.39 | 8 | 0 |
Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than one hour, caused by transient thrombotic or embolic blood vessel occlusion or stenosis. Events may be classified by arterial distribution, temporal pattern, or etiology (e.g., embolic vs. thrombotic). (From Adams et al., Principles of Neurology, 6th ed, pp814-6) | 0 | 4.39 | 8 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 2.07 | 1 | 0 |
Benign Neoplasms [description not available] | 0 | 6.76 | 10 | 1 |
Nicotine Addiction [description not available] | 0 | 2.07 | 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 | 6.76 | 10 | 1 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 2.07 | 1 | 0 |
Masked Hypertension Phenomenon where increased BLOOD PRESSURE readings taken in non-clinical settings (e.g., HOME BLOOD PRESSURE MONITORING) do not replicate in clinical settings. | 0 | 3.46 | 1 | 1 |
Bewilderment [description not available] | 0 | 2.39 | 2 | 0 |
Tachycardia, Supraventricular A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | 0 | 2.71 | 3 | 0 |
Benign Meningeal Neoplasms [description not available] | 0 | 2.39 | 2 | 0 |
Angioblastic Meningioma [description not available] | 0 | 2.07 | 1 | 0 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 2.39 | 2 | 0 |
Meningioma A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7) | 0 | 2.07 | 1 | 0 |
Arrhythmia, Sinoatrial [description not available] | 0 | 4.9 | 14 | 0 |
Hemorrhage, Uterine [description not available] | 0 | 2.68 | 3 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 2.68 | 3 | 0 |
Benign Supratentorial Neoplasms [description not available] | 0 | 2.1 | 1 | 0 |
Chylothorax The presence of chyle in the thoracic cavity. (Dorland, 27th ed) | 0 | 2.07 | 1 | 0 |
Craniofacial Microsomia [description not available] | 0 | 2.99 | 1 | 0 |
Franceschetti-Zwahlen-Klein Syndrome [description not available] | 0 | 2.99 | 1 | 0 |
Congenital Micrognathia [description not available] | 0 | 4.67 | 11 | 0 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 9.27 | 7 | 0 |
Infections, Pseudomonas [description not available] | 0 | 2.65 | 3 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 2.65 | 3 | 0 |
Kahler Disease [description not available] | 0 | 3.47 | 1 | 1 |
Multiple Myeloma A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 3.47 | 1 | 1 |
Beuren Syndrome [description not available] | 0 | 7.08 | 1 | 0 |
Bronchial Pneumonia [description not available] | 0 | 4.37 | 8 | 0 |
Abnormalities, Congenital [description not available] | 0 | 3.66 | 10 | 0 |
Pyloric Stenosis Narrowing of the pyloric canal with varied etiology. A common form is due to muscle hypertrophy (PYLORIC STENOSIS, HYPERTROPHIC) seen in infants. | 0 | 4.97 | 9 | 1 |
Acquired Vocal Cord Palsy [description not available] | 0 | 4.5 | 9 | 0 |
Vocal Cord Paralysis Congenital or acquired paralysis of one or both VOCAL CORDS. This condition is caused by defects in the CENTRAL NERVOUS SYSTEM, the VAGUS NERVE and branches of LARYNGEAL NERVES. Common symptoms are VOICE DISORDERS including HOARSENESS or APHONIA. | 0 | 9.5 | 9 | 0 |
Convalescence The period of recovery following an illness. | 0 | 3.29 | 2 | 0 |
Fungus Poisoning [description not available] | 0 | 3.34 | 2 | 0 |
Fungal Lung Diseases [description not available] | 0 | 2.01 | 1 | 0 |
Lactic Acidosis [description not available] | 0 | 2.68 | 3 | 0 |
Acidosis, Lactic Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. It may occur spontaneously or in association with diseases such as DIABETES MELLITUS; LEUKEMIA; or LIVER FAILURE. | 0 | 2.68 | 3 | 0 |
Coagulation Disorders, Blood [description not available] | 0 | 4.45 | 5 | 1 |
Hydatid Mole [description not available] | 0 | 2.01 | 1 | 0 |
Blood Coagulation Disorders Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions. | 0 | 4.45 | 5 | 1 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 2.01 | 1 | 0 |
Cataract, Membranous [description not available] | 0 | 2.89 | 4 | 0 |
Cataract Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed) | 0 | 2.89 | 4 | 0 |
Phlegmon [description not available] | 0 | 2.01 | 1 | 0 |
Dacryoadenitis [description not available] | 0 | 2.01 | 1 | 0 |
Lacrimal Duct Obstruction Interference with the secretion of tears by the lacrimal glands. Obstruction of the LACRIMAL SAC or NASOLACRIMAL DUCT causing acute or chronic inflammation of the lacrimal sac (DACRYOCYSTITIS). It is caused also in infants by failure of the nasolacrimal duct to open into the inferior meatus and occurs about the third week of life. In adults occlusion may occur spontaneously or after injury or nasal disease. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p250) | 0 | 2.01 | 1 | 0 |
Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. | 0 | 2.01 | 1 | 0 |
Colitis, Granulomatous [description not available] | 0 | 2.01 | 1 | 0 |
Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients. | 0 | 2.01 | 1 | 0 |
Health Care Associated Infection [description not available] | 0 | 3.09 | 5 | 0 |
Acute Hepatic Failure [description not available] | 0 | 2.01 | 1 | 0 |
Cronobacter Infections [description not available] | 0 | 2.01 | 1 | 0 |
Echo Virus Infections [description not available] | 0 | 2.39 | 2 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 3.09 | 5 | 0 |
Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | 0 | 2.01 | 1 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 2.01 | 1 | 0 |
Liver Failure, Acute A form of rapid-onset LIVER FAILURE, also known as fulminant hepatic failure, caused by severe liver injury or massive loss of HEPATOCYTES. It is characterized by sudden development of liver dysfunction and JAUNDICE. Acute liver failure may progress to exhibit cerebral dysfunction even HEPATIC COMA depending on the etiology that includes hepatic ISCHEMIA, drug toxicity, malignant infiltration, and viral hepatitis such as post-transfusion HEPATITIS B and HEPATITIS C. | 0 | 2.01 | 1 | 0 |
Middle Ear Inflammation [description not available] | 0 | 3.33 | 2 | 0 |
Sinus Infections [description not available] | 0 | 2.93 | 1 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 3.33 | 2 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 2.93 | 1 | 0 |
Bronchial Hyperreactivity Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory. | 0 | 4.72 | 2 | 1 |
Behavior Disorder, Rapid Eye Movement Sleep [description not available] | 0 | 2.01 | 1 | 0 |
REM Sleep Behavior Disorder A disorder characterized by episodes of vigorous and often violent motor activity during REM sleep (SLEEP, REM). The affected individual may inflict self injury or harm others, and is difficult to awaken from this condition. Episodes are usually followed by a vivid recollection of a dream that is consistent with the aggressive behavior. This condition primarily affects adult males. (From Adams et al., Principles of Neurology, 6th ed, p393) | 0 | 2.01 | 1 | 0 |
Narcosis A state of depressed CENTRAL NERVOUS SYSTEM marked by stupor or insensibility. | 0 | 2.84 | 4 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 4.26 | 4 | 1 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 2.62 | 3 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 4.26 | 4 | 1 |
Complications, Labor [description not available] | 0 | 4.12 | 6 | 0 |
Anton Syndrome [description not available] | 0 | 1.93 | 1 | 0 |
Bouillaud Disease [description not available] | 0 | 2.34 | 2 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 2.63 | 3 | 0 |
Rheumatic Heart Disease Cardiac manifestation of systemic rheumatological conditions, such as RHEUMATIC FEVER. Rheumatic heart disease can involve any part the heart, most often the HEART VALVES and the ENDOCARDIUM. | 0 | 2.34 | 2 | 0 |
Anuria Absence of urine formation. It is usually associated with complete bilateral ureteral (URETER) obstruction, complete lower urinary tract obstruction, or unilateral ureteral obstruction when a solitary kidney is present. | 0 | 7.85 | 4 | 0 |
Encephalitis, Polio [description not available] | 0 | 1.93 | 1 | 0 |
Clostridium tetani Infection [description not available] | 0 | 3.45 | 8 | 0 |
Bulbar Polio [description not available] | 0 | 1.93 | 1 | 0 |
Poliomyelitis An acute infectious disease of humans, particularly children, caused by any of three serotypes of human poliovirus (POLIOVIRUS). Usually the infection is limited to the gastrointestinal tract and nasopharynx, and is often asymptomatic. The central nervous system, primarily the spinal cord, may be affected, leading to rapidly progressive paralysis, coarse FASCICULATION and hyporeflexia. Motor neurons are primarily affected. Encephalitis may also occur. The virus replicates in the nervous system, and may cause significant neuronal loss, most notably in the spinal cord. A rare related condition, nonpoliovirus poliomyelitis, may result from infections with nonpoliovirus enteroviruses. (From Adams et al., Principles of Neurology, 6th ed, pp764-5) | 0 | 1.93 | 1 | 0 |
Tetanus A disease caused by tetanospasmin, a powerful protein toxin produced by CLOSTRIDIUM TETANI. Tetanus usually occurs after an acute injury, such as a puncture wound or laceration. Generalized tetanus, the most common form, is characterized by tetanic muscular contractions and hyperreflexia. Localized tetanus presents itself as a mild condition with manifestations restricted to muscles near the wound. It may progress to the generalized form. | 0 | 3.45 | 8 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 3.44 | 8 | 0 |
Bodily Distress Disorder [description not available] | 0 | 1.93 | 1 | 0 |
Incompetence, Pulmonary Valve [description not available] | 0 | 2.34 | 2 | 0 |
Koch's Disease [description not available] | 0 | 2.64 | 3 | 0 |
Pulmonary Consumption [description not available] | 0 | 3.55 | 3 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 7.64 | 3 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 3.55 | 3 | 0 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 1.93 | 1 | 0 |
Dystocia Slow or difficult OBSTETRIC LABOR or CHILDBIRTH. | 0 | 1.93 | 1 | 0 |
Buphthalmos [description not available] | 0 | 1.93 | 1 | 0 |
Mitral Incompetence [description not available] | 0 | 4.24 | 7 | 0 |
Mitral Stenosis [description not available] | 0 | 3.04 | 5 | 0 |
Mitral Valve Insufficiency Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation. | 0 | 4.24 | 7 | 0 |
Mitral Valve Stenosis Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause. | 0 | 3.04 | 5 | 0 |
Thyroglossal Cyst A cyst in the neck caused by persistence of portions of, or by lack of closure of, the primitive thyroglossal duct. (Dorland, 27th ed) | 0 | 3.07 | 5 | 0 |
Cancer of the Tongue [description not available] | 0 | 2.34 | 2 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 2.34 | 2 | 0 |
Diseases, Occupational [description not available] | 0 | 3.21 | 6 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 4.73 | 12 | 0 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 2.63 | 3 | 0 |
Cor Pulmonale [description not available] | 0 | 4.83 | 8 | 0 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 5.97 | 15 | 2 |
Pericarditis Inflammation of the PERICARDIUM from various origins, such as infection, neoplasm, autoimmune process, injuries, or drug-induced. Pericarditis usually leads to PERICARDIAL EFFUSION, or CONSTRICTIVE PERICARDITIS. | 0 | 2.63 | 3 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 2.64 | 3 | 0 |
Aneurysm Pathological outpouching or sac-like dilatation in the wall of any blood vessel (ARTERIES or VEINS) or the heart (HEART ANEURYSM). It indicates a thin and weakened area in the wall which may later rupture. Aneurysms are classified by location, etiology, or other characteristics. | 0 | 2.64 | 3 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 3.75 | 2 | 1 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 2.86 | 4 | 0 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 2.64 | 3 | 0 |
Brain Emboli [description not available] | 0 | 1.94 | 1 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 2.64 | 3 | 0 |
Gastric Ulcer [description not available] | 0 | 8.81 | 4 | 0 |
Peptic Ulcer Perforation Penetration of a PEPTIC ULCER through the wall of DUODENUM or STOMACH allowing the leakage of luminal contents into the PERITONEAL CAVITY. | 0 | 1.93 | 1 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 3.81 | 4 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 6.02 | 20 | 0 |
Brain Neoplasms Neoplasms of the intracranial components of the central nervous system, including the cerebral hemispheres, basal ganglia, hypothalamus, thalamus, brain stem, and cerebellum. Brain neoplasms are subdivided into primary (originating from brain tissue) and secondary (i.e., metastatic) forms. Primary neoplasms are subdivided into benign and malignant forms. In general, brain tumors may also be classified by age of onset, histologic type, or presenting location in the brain. | 0 | 6.02 | 20 | 0 |
Emphysema, Mediastinal [description not available] | 0 | 3.8 | 4 | 0 |
Abortion, Tubal [description not available] | 0 | 1.93 | 1 | 0 |
Abortion, Threatened UTERINE BLEEDING from a GESTATION of less than 20 weeks without any CERVICAL DILATATION. It is characterized by vaginal bleeding, lower back discomfort, or midline pelvic cramping and a risk factor for MISCARRIAGE. | 0 | 1.93 | 1 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 1.93 | 1 | 0 |
Brain Inflammation [description not available] | 0 | 3.05 | 5 | 0 |
Rubeola [description not available] | 0 | 1.94 | 1 | 0 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 3.05 | 5 | 0 |
Measles A highly contagious infectious disease caused by MORBILLIVIRUS, common among children but also seen in the nonimmune of any age, in which the virus enters the respiratory tract via droplet nuclei and multiplies in the epithelial cells, spreading throughout the MONONUCLEAR PHAGOCYTE SYSTEM. | 0 | 1.94 | 1 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 2.64 | 3 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 2.64 | 3 | 0 |
Pyoderma Any purulent skin disease (Dorland, 27th ed). | 0 | 1.94 | 1 | 0 |
Neuroses [description not available] | 0 | 1.93 | 1 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 1.93 | 1 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 1.94 | 1 | 0 |
Cancer of Rectum [description not available] | 0 | 2.36 | 2 | 0 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 2.36 | 2 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 3.57 | 3 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 3.57 | 3 | 0 |
Cushing's Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Aldosteronism [description not available] | 0 | 3.28 | 2 | 0 |
Potassium Deficiency A condition due to decreased dietary intake of potassium, as in starvation or failure to administer in intravenous solutions, or to gastrointestinal loss in diarrhea, chronic laxative abuse, vomiting, gastric suction, or bowel diversion. Severe potassium deficiency may produce muscular weakness and lead to paralysis and respiratory failure. Muscular malfunction may result in hypoventilation, paralytic ileus, hypotension, muscle twitches, tetany, and rhabomyolysis. Nephropathy from potassium deficit impairs the concentrating mechanism, producing POLYURIA and decreased maximal urinary concentrating ability with secondary POLYDIPSIA. (Merck Manual, 16th ed) | 0 | 2.34 | 2 | 0 |
Adrenal Gland Hyperfunction [description not available] | 0 | 2.64 | 3 | 0 |
Adrenocortical Hyperfunction Excess production of ADRENAL CORTEX HORMONES such as ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE. Hyperadrenal syndromes include CUSHING SYNDROME; HYPERALDOSTERONISM; and VIRILISM. | 0 | 2.64 | 3 | 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 | 1.94 | 1 | 0 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 3.28 | 2 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 2.36 | 2 | 0 |
Fracture, Pathologic [description not available] | 0 | 2.34 | 2 | 0 |
Injuries, Spinal [description not available] | 0 | 2.35 | 2 | 0 |
Catatonia A neuropsychiatric disorder characterized by one or more of the following essential features: immobility, mutism, negativism (active or passive refusal to follow commands), mannerisms, stereotypies, posturing, grimacing, excitement, echolalia, echopraxia, muscular rigidity, and stupor; sometimes punctuated by sudden violent outbursts, panic, or hallucinations. This condition may be associated with psychiatric illnesses (e.g., SCHIZOPHRENIA; MOOD DISORDERS) or organic disorders (NEUROLEPTIC MALIGNANT SYNDROME; ENCEPHALITIS, etc.). (From DSM-IV, 4th ed, 1994; APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 2.35 | 2 | 0 |
Paranoia [description not available] | 0 | 2.35 | 2 | 0 |
Psychoses [description not available] | 0 | 2.63 | 3 | 0 |
Dementia Praecox [description not available] | 0 | 3.06 | 5 | 0 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 2.63 | 3 | 0 |
Schizophrenia A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. | 0 | 3.06 | 5 | 0 |
Urinary Incontinence Involuntary loss of URINE, such as leaking of urine. It is a symptom of various underlying pathological processes. Major types of incontinence include URINARY URGE INCONTINENCE and URINARY STRESS INCONTINENCE. | 0 | 3.8 | 4 | 0 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 2.65 | 3 | 0 |
Intracranial Aneurysm Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms ( | 0 | 2.65 | 3 | 0 |
Deficiency Diseases A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 3.96 | 5 | 0 |
Abscess, Hepatic [description not available] | 0 | 1.94 | 1 | 0 |
Abscess, Amebic, Hepatic [description not available] | 0 | 1.94 | 1 | 0 |
Lung Diseases, Parasitic Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS). | 0 | 1.94 | 1 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 1.94 | 1 | 0 |
Carotid Artery Thrombosis Blood clot formation in any part of the CAROTID ARTERIES. This may produce CAROTID STENOSIS or occlusion of the vessel, leading to TRANSIENT ISCHEMIC ATTACK; CEREBRAL INFARCTION; or AMAUROSIS FUGAX. | 0 | 2.34 | 2 | 0 |
Mandibular Retroposition [description not available] | 0 | 3.05 | 5 | 0 |
Cerebromeningitis [description not available] | 0 | 2.36 | 2 | 0 |
Obesity Hypoventilation Syndrome HYPOVENTILATION syndrome in very obese persons with excessive ADIPOSE TISSUE around the ABDOMEN and DIAPHRAGM. It is characterized by diminished to absent ventilatory chemoresponsiveness; chronic HYPOXIA; HYPERCAPNIA; POLYCYTHEMIA; and long periods of sleep during day and night (HYPERSOMNOLENCE). It is a condition often related to OBSTRUCTIVE SLEEP APNEA but can occur separately. | 0 | 6.14 | 23 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 2.64 | 3 | 0 |
Sarcoidosis An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands. | 0 | 2.64 | 3 | 0 |
Erythrocytosis [description not available] | 0 | 2.64 | 3 | 0 |
Embolus [description not available] | 0 | 1.94 | 1 | 0 |
Embolism Blocking of a blood vessel by an embolus which can be a blood clot or other undissolved material in the blood stream. | 0 | 1.94 | 1 | 0 |
Extravascular Hemolysis [description not available] | 0 | 2.34 | 2 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 2.34 | 2 | 0 |
Tracheitis INFLAMMATION of the TRACHEA that is usually associated with RESPIRATORY TRACT INFECTIONS. | 0 | 2.64 | 3 | 0 |
Hypernatremia Excessive amount of sodium in the blood. (Dorland, 27th ed) | 0 | 2.37 | 2 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 3.05 | 5 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 3.05 | 5 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 2.35 | 2 | 0 |
Esophageal Hernia [description not available] | 0 | 2.64 | 3 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 2.35 | 2 | 0 |
Hypopituitarism Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions. | 0 | 2.35 | 2 | 0 |
Lacerations Torn, ragged, mangled wounds. | 0 | 1.93 | 1 | 0 |
Cranial Epidural Hematoma [description not available] | 0 | 4.04 | 3 | 0 |
Battered Child Syndrome A clinical condition resulting from repeated physical and psychological injuries inflicted on a child by the parents or caregivers. | 0 | 3.61 | 3 | 0 |
Aerophagy Spasmodic swallowing of air. | 0 | 2.41 | 2 | 0 |
Anal Atresia [description not available] | 0 | 2.01 | 1 | 0 |
Bladder Exstrophy A birth defect in which the URINARY BLADDER is malformed and exposed, inside out, and protruded through the ABDOMINAL WALL. It is caused by closure defects involving the top front surface of the bladder, as well as the lower abdominal wall; SKIN; MUSCLES; and the pubic bone. | 0 | 2.39 | 2 | 0 |
Acquired Meningocele [description not available] | 0 | 2.01 | 1 | 0 |
Abnormalities, Digestive System [description not available] | 0 | 2.01 | 1 | 0 |
Arousal Disorders, Sleep [description not available] | 0 | 2.42 | 2 | 0 |
Spasmophilia [description not available] | 0 | 2.85 | 4 | 0 |
Psychoses, Drug [description not available] | 0 | 2.34 | 2 | 0 |
Libman-Sacks Disease [description not available] | 0 | 3.58 | 3 | 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 | 3.58 | 3 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 3.6 | 3 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 3.6 | 3 | 0 |
Nanism [description not available] | 0 | 4.06 | 3 | 0 |
Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. | 0 | 4.06 | 3 | 0 |
Calcification, Pathologic [description not available] | 0 | 2.02 | 1 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 2.02 | 1 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 2.93 | 1 | 0 |
Cerebromalacia [description not available] | 0 | 2.37 | 2 | 0 |
Autism [description not available] | 0 | 2.39 | 2 | 0 |
Absence Seizure Disorder [description not available] | 0 | 4.12 | 6 | 0 |
Autistic Disorder A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V) | 0 | 2.39 | 2 | 0 |
Epilepsy, Absence A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736) | 0 | 4.12 | 6 | 0 |
Stunted Growth [description not available] | 0 | 3.21 | 6 | 0 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 3.21 | 6 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 3.6 | 3 | 0 |
HMN (Hereditary Motor Neuropathy) Proximal Type I [description not available] | 0 | 2.02 | 1 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 3.6 | 3 | 0 |
Spinal Muscular Atrophies of Childhood A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3) | 0 | 2.02 | 1 | 0 |
Ataxia Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions. | 0 | 3.57 | 9 | 0 |
Depression, Endogenous [description not available] | 0 | 2.34 | 2 | 0 |
Depressive Disorder An affective disorder manifested by either a dysphoric mood or loss of interest or pleasure in usual activities. The mood disturbance is prominent and relatively persistent. | 0 | 2.34 | 2 | 0 |
Adolescent Myoclonic Epilepsy [description not available] | 0 | 2.02 | 1 | 0 |
Conjugate Nystagmus [description not available] | 0 | 3.08 | 5 | 0 |
Developmental Psychomotor Disorders [description not available] | 0 | 3.48 | 8 | 0 |
Dyskinesia, Medication-Induced [description not available] | 0 | 2.67 | 3 | 0 |
Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199) | 0 | 2.67 | 3 | 0 |
Academic Disorder, Developmental [description not available] | 0 | 4.3 | 4 | 0 |
Learning Disabilities Conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills. These may result from organic or psychological conditions. Relatively common subtypes include DYSLEXIA, DYSCALCULIA, and DYSGRAPHIA. | 0 | 4.3 | 4 | 0 |
Nonsynostotic Plagiocephaly [description not available] | 0 | 2.94 | 1 | 0 |
Congenital Oculofacial Paralysis, Moebius [description not available] | 0 | 2.02 | 1 | 0 |
Benign Infratentorial Neoplasms [description not available] | 0 | 2.02 | 1 | 0 |
Brain Abscess A circumscribed collection of purulent exudate in the brain, due to bacterial and other infections. The majority are caused by spread of infected material from a focus of suppuration elsewhere in the body, notably the PARANASAL SINUSES, middle ear (see EAR, MIDDLE); HEART (see also ENDOCARDITIS, BACTERIAL), and LUNG. Penetrating CRANIOCEREBRAL TRAUMA and NEUROSURGICAL PROCEDURES may also be associated with this condition. Clinical manifestations include HEADACHE; SEIZURES; focal neurologic deficits; and alterations of consciousness. (Adams et al., Principles of Neurology, 6th ed, pp712-6) | 0 | 2.02 | 1 | 0 |
Atrial Septal Defect [description not available] | 0 | 2.02 | 1 | 0 |
Exanthem [description not available] | 0 | 2.02 | 1 | 0 |
Enterocolitis Inflammation of the MUCOSA of both the SMALL INTESTINE and the LARGE INTESTINE. Etiology includes ISCHEMIA, infections, allergic, and immune responses. | 0 | 2.02 | 1 | 0 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 2.02 | 1 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 3.8 | 4 | 0 |
Purpura Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is | 0 | 3.8 | 4 | 0 |
Complete Breech [description not available] | 0 | 2.38 | 2 | 0 |
Breech Presentation A malpresentation of the FETUS at near term or during OBSTETRIC LABOR with the fetal cephalic pole in the fundus of the UTERUS. There are three types of breech: the complete breech with flexed hips and knees; the incomplete breech with one or both hips partially or fully extended; the frank breech with flexed hips and extended knees. | 0 | 2.38 | 2 | 0 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 2.03 | 1 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 2.02 | 1 | 0 |
Cancer of Pituitary [description not available] | 0 | 2.02 | 1 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 2.02 | 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 | 2.02 | 1 | 0 |
Acquired Language Disorders [description not available] | 0 | 2.03 | 1 | 0 |
Language Disorders Conditions characterized by deficiencies of comprehension or expression of written and spoken forms of language. These include acquired and developmental disorders. | 0 | 2.03 | 1 | 0 |
Fibroid [description not available] | 0 | 2.37 | 2 | 0 |
Leiomyoma A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues. | 0 | 2.37 | 2 | 0 |
Brain Vascular Disorders [description not available] | 0 | 5.29 | 13 | 1 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 5.29 | 13 | 1 |
Rachitis [description not available] | 0 | 2.65 | 3 | 0 |
Cancer of Head [description not available] | 0 | 4.67 | 2 | 1 |
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 | 4.67 | 2 | 1 |
Bronchospasm [description not available] | 0 | 9.95 | 15 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 2.02 | 1 | 0 |
Anorectal Diseases [description not available] | 0 | 2.02 | 1 | 0 |
Drooling [description not available] | 0 | 3.35 | 2 | 0 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 4.95 | 15 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 2.02 | 1 | 0 |
Sialorrhea Increased salivary flow. | 0 | 3.35 | 2 | 0 |
Dystonia An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77) | 0 | 7.64 | 5 | 4 |
Acute Edematous Pancreatitis [description not available] | 0 | 3.56 | 3 | 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 | 3.56 | 3 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 2.03 | 1 | 0 |
Thrombopenia [description not available] | 0 | 3.08 | 5 | 0 |
Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder. | 0 | 2.03 | 1 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 8.08 | 5 | 0 |
Decapitation Traumatic or experimentally induced separation of the head from the body in an animal or human. | 0 | 2.42 | 2 | 0 |
Water Intoxication A condition resulting from the excessive retention of water with sodium depletion. | 0 | 2.03 | 1 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 7.03 | 1 | 0 |
Gallstone Disease [description not available] | 0 | 2.03 | 1 | 0 |
Clubfeet [description not available] | 0 | 2.03 | 1 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 2.03 | 1 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 2.37 | 2 | 0 |
Fra(X) Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
Fragile X Syndrome A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226) | 0 | 2.03 | 1 | 0 |
Genetic Diseases [description not available] | 0 | 2.03 | 1 | 0 |
Colitis Gravis [description not available] | 0 | 2.03 | 1 | 0 |
Colitis, Ulcerative Inflammation of the COLON that is predominantly confined to the MUCOSA. Its major symptoms include DIARRHEA, rectal BLEEDING, the passage of MUCUS, and ABDOMINAL PAIN. | 0 | 2.03 | 1 | 0 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 2.03 | 1 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 3.76 | 2 | 0 |
Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. | 0 | 4.59 | 6 | 0 |
Capillary Telangiectasia, Brain [description not available] | 0 | 2.03 | 1 | 0 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 2.03 | 1 | 0 |
Aortic Incompetence [description not available] | 0 | 3.06 | 5 | 0 |
Classic Galactosemia [description not available] | 0 | 2.03 | 1 | 0 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 2.4 | 2 | 0 |
Foot Injuries General or unspecified injuries involving the foot. | 0 | 2.03 | 1 | 0 |
Aortic Valve Insufficiency Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root). | 0 | 3.06 | 5 | 0 |
Diverticulitis Inflammation of a DIVERTICULUM or diverticula. | 0 | 2.37 | 2 | 0 |
Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) | 0 | 2.03 | 1 | 0 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 2.39 | 2 | 0 |
Bladder Calculi [description not available] | 0 | 2.03 | 1 | 0 |
Exertional Heat Illness [description not available] | 0 | 2.03 | 1 | 0 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 2.94 | 1 | 0 |
Fibromyalgia A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscle pain is typically aggravated by inactivity or exposure to cold. This condition is often associated with general symptoms, such as sleep disturbances, fatigue, stiffness, HEADACHES, and occasionally DEPRESSION. There is significant overlap between fibromyalgia and the chronic fatigue syndrome (FATIGUE SYNDROME, CHRONIC). Fibromyalgia may arise as a primary or secondary disease process. It is most frequent in females aged 20 to 50 years. (From Adams et al., Principles of Neurology, 6th ed, p1494-95) | 0 | 2.94 | 1 | 0 |
Central Pontine Myelinolysis [description not available] | 0 | 2.03 | 1 | 0 |
Alexander Disease Rare leukoencephalopathy with infantile-onset accumulation of Rosenthal fibers in the subpial, periventricular, and subependymal zones of the brain. Rosenthal fibers are GLIAL FIBRILLARY ACIDIC PROTEIN aggregates found in ASTROCYTES. Juvenile- and adult-onset types show progressive atrophy of the lower brainstem instead. De novo mutations in the GFAP gene are associated with the disease with propensity for paternal inheritance. | 0 | 2.03 | 1 | 0 |
Wallerian Degeneration Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH. | 0 | 2.03 | 1 | 0 |
Anorexia The lack or loss of APPETITE accompanied by an aversion to food and the inability to eat. It is the defining characteristic of the disorder ANOREXIA NERVOSA. | 0 | 2.4 | 2 | 0 |
HbS Disease [description not available] | 0 | 3.8 | 4 | 0 |
Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. | 0 | 3.8 | 4 | 0 |
Priapism A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments. | 0 | 2.94 | 1 | 0 |
Bordetella Infections Infections with bacteria of the genus BORDETELLA. | 0 | 2.37 | 2 | 0 |
Glial Cell Tumors [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Cardiometabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components not only include metabolic dysfunctions of METABOLIC SYNDROME but also HYPERTENSION, and ABDOMINAL OBESITY. | 0 | 2.95 | 1 | 0 |
Liver Steatosis [description not available] | 0 | 3.99 | 5 | 0 |
Acquired Adult Flatfoot Deformity [description not available] | 0 | 2.95 | 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 | 3.99 | 5 | 0 |
Metabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome include ABDOMINAL OBESITY; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. | 0 | 2.95 | 1 | 0 |
Agricultural Worker Disease [description not available] | 0 | 2.03 | 1 | 0 |
47,XX,+21 [description not available] | 0 | 3.35 | 2 | 0 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 3.35 | 2 | 0 |
Alcohol-Induced Disorders Disorders stemming from the misuse and abuse of alcohol. | 0 | 2.02 | 1 | 0 |
Gasser Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 2.37 | 2 | 0 |
Lymphocytosis Excess of normal lymphocytes in the blood or in any effusion. | 0 | 2.03 | 1 | 0 |
Hemolytic-Uremic Syndrome A syndrome that is associated with microvascular diseases of the KIDNEY, such as RENAL CORTICAL NECROSIS. It is characterized by hemolytic anemia (ANEMIA, HEMOLYTIC); THROMBOCYTOPENIA; and ACUTE RENAL FAILURE. | 0 | 2.03 | 1 | 0 |
Hematoma, Subdural, Cranial [description not available] | 0 | 2.95 | 1 | 0 |
Hematoma, Subdural, Intracranial Accumulation of blood in the SUBDURAL SPACE over the CEREBRAL HEMISPHERE. | 0 | 2.95 | 1 | 0 |
Abdominal Migraine [description not available] | 0 | 3.3 | 2 | 0 |
Migraine Disorders A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 3.3 | 2 | 0 |
Infections, Paramyxoviridae [description not available] | 0 | 2.41 | 2 | 0 |
Paramyxoviridae Infections Infections with viruses of the family PARAMYXOVIRIDAE. This includes MORBILLIVIRUS INFECTIONS; RESPIROVIRUS INFECTIONS; PNEUMOVIRUS INFECTIONS; HENIPAVIRUS INFECTIONS; AVULAVIRUS INFECTIONS; and RUBULAVIRUS INFECTIONS. | 0 | 2.41 | 2 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 3.82 | 4 | 0 |
Ganglioglioma Rare indolent tumors comprised of neoplastic glial and neuronal cells which occur primarily in children and young adults. Benign lesions tend to be associated with long survival unless the tumor degenerates into a histologically malignant form. They tend to occur in the optic nerve and white matter of the brain and spinal cord. | 0 | 2.44 | 2 | 0 |
Astrocytoma Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082) | 0 | 8.82 | 4 | 0 |
Brucella Infection [description not available] | 0 | 2.03 | 1 | 0 |
Cranial Nerve Diseases Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain stem nuclei from which the cranial nerves originate or terminate. | 0 | 3.61 | 3 | 0 |
Autoimmune Demyelinating Disease, Peripheral [description not available] | 0 | 2.03 | 1 | 0 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 2.03 | 1 | 0 |
Flexor Tendon Entrapment [description not available] | 0 | 2.04 | 1 | 0 |
Myelopathy [description not available] | 0 | 3.58 | 3 | 0 |
Spinal Cord Diseases Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. | 0 | 3.58 | 3 | 0 |
Albers-Schoenberg Disease [description not available] | 0 | 2.04 | 1 | 0 |
Osteopetrosis Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). | 0 | 2.04 | 1 | 0 |
Angiitis [description not available] | 0 | 2.04 | 1 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 2.04 | 1 | 0 |
Adipocere [description not available] | 0 | 2.68 | 3 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 3.34 | 2 | 0 |
Diverticula [description not available] | 0 | 2.39 | 2 | 0 |
Tracheal Diseases Diseases involving the TRACHEA. | 0 | 4.9 | 14 | 0 |
Aortic Arch Syndrome [description not available] | 0 | 2.04 | 1 | 0 |
DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. | 0 | 3.34 | 2 | 0 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 4.59 | 6 | 1 |
Thoracic Diseases Disorders affecting the organs of the thorax. | 0 | 2.34 | 2 | 0 |
Altidudinal Hemianopia [description not available] | 0 | 1.94 | 1 | 0 |
Infarct [description not available] | 0 | 2.34 | 2 | 0 |
Muscular Dystrophy [description not available] | 0 | 3.56 | 3 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 1.94 | 1 | 0 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 2.35 | 2 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 3.56 | 3 | 0 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 1.94 | 1 | 0 |
Fetal Distress A nonreassuring fetal status (NRFS) indicating that the FETUS is compromised (American College of Obstetricians and Gynecologists 1988). It can be identified by sub-optimal values in FETAL HEART RATE; oxygenation of FETAL BLOOD; and other parameters. | 0 | 4.03 | 3 | 1 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 3.2 | 6 | 0 |
Huntington Disease A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) | 0 | 3.2 | 6 | 0 |
Abdominal Injuries General or unspecified injuries involving organs in the abdominal cavity. | 0 | 2.65 | 3 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 2.37 | 2 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 1.96 | 1 | 0 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 2.37 | 2 | 0 |
Carcinoma, Intraductal, Noninfiltrating A noninvasive (noninfiltrating) carcinoma of the breast characterized by a proliferation of malignant epithelial cells confined to the mammary ducts or lobules, without light-microscopy evidence of invasion through the basement membrane into the surrounding stroma. | 0 | 1.96 | 1 | 0 |
Alkalosis, Respiratory A state due to excess loss of carbon dioxide from the body. (Dorland, 27th ed) | 0 | 4.25 | 4 | 0 |
Alcoholic Liver Diseases [description not available] | 0 | 2.88 | 1 | 0 |
Liver Diseases, Alcoholic Liver diseases associated with ALCOHOLISM. It usually refers to the coexistence of two or more subentities, i.e., ALCOHOLIC FATTY LIVER; ALCOHOLIC HEPATITIS; and ALCOHOLIC CIRRHOSIS. | 0 | 2.88 | 1 | 0 |
Diseases of Endocrine System [description not available] | 0 | 2.88 | 1 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 2.88 | 1 | 0 |
Absence of Brain, Congenital [description not available] | 0 | 4.05 | 3 | 0 |
Deficiency, Vitamin E [description not available] | 0 | 2.88 | 1 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 2.88 | 1 | 0 |
Brown Lung [description not available] | 0 | 1.96 | 1 | 0 |
Adam-Stokes Attacks [description not available] | 0 | 2.36 | 2 | 0 |
Amentia [description not available] | 0 | 2.37 | 2 | 0 |
Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness. | 0 | 2.37 | 2 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 2.66 | 3 | 0 |
Tracheal Neoplasms New abnormal growth of tissue in the TRACHEA. | 0 | 3.79 | 4 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 3.98 | 5 | 0 |
Epiglottitis Inflammation of the EPIGLOTTIS. | 0 | 1.96 | 1 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 3.97 | 5 | 0 |
Enterocolitis, Pseudomembranous An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization. | 0 | 3.97 | 5 | 0 |
Muscle Spasm [description not available] | 0 | 5.45 | 11 | 0 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 5.45 | 11 | 0 |
Dysplasia Linguofacialis [description not available] | 0 | 2.37 | 2 | 0 |
Esophagitis, Reflux [description not available] | 0 | 2.36 | 2 | 0 |
Esophagitis, Peptic INFLAMMATION of the ESOPHAGUS that is caused by the reflux of GASTRIC JUICE with contents of the STOMACH and DUODENUM. | 0 | 2.36 | 2 | 0 |
Diseases of Pharynx [description not available] | 0 | 2.36 | 2 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 7.82 | 24 | 1 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 7.82 | 24 | 1 |
Hyperkyphosis [description not available] | 0 | 2.36 | 2 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 2.65 | 3 | 0 |
Active Hyperemia [description not available] | 0 | 2.64 | 3 | 0 |
Mast-Cell Sarcoma A unifocal malignant tumor that consists of atypical pathological MAST CELLS without systemic involvement. It causes local destructive growth in organs other than in skin or bone marrow. | 0 | 1.96 | 1 | 0 |
Hyperemia The presence of an increased amount of blood in a body part or an organ leading to congestion or engorgement of blood vessels. Hyperemia can be due to increase of blood flow into the area (active or arterial), or due to obstruction of outflow of blood from the area (passive or venous). | 0 | 2.64 | 3 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 2.87 | 1 | 0 |
Arthropathies [description not available] | 0 | 1.96 | 1 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 1.96 | 1 | 0 |
Cretinism [description not available] | 0 | 2.36 | 2 | 0 |
Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. | 0 | 2.36 | 2 | 0 |
Facial Injuries General or unspecified injuries to the soft tissue or bony portions of the face. | 0 | 2.36 | 2 | 0 |
Mandibular Fractures Fractures of the lower jaw. | 0 | 2.36 | 2 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 4.72 | 7 | 0 |
Kaposi Sarcoma [description not available] | 0 | 1.96 | 1 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 4.72 | 7 | 0 |
Sarcoma, Kaposi A multicentric, malignant neoplastic vascular proliferation characterized by the development of bluish-red cutaneous nodules, usually on the lower extremities, most often on the toes or feet, and slowly increasing in size and number and spreading to more proximal areas. The tumors have endothelium-lined channels and vascular spaces admixed with variably sized aggregates of spindle-shaped cells, and often remain confined to the skin and subcutaneous tissue, but widespread visceral involvement may occur. Kaposi's sarcoma occurs spontaneously in Jewish and Italian males in Europe and the United States. An aggressive variant in young children is endemic in some areas of Africa. A third form occurs in about 0.04% of kidney transplant patients. There is also a high incidence in AIDS patients. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, pp2105-7) HHV-8 is the suspected cause. | 0 | 1.96 | 1 | 0 |
Infant Malnutrition Malnutrition, occurring in infants ages 1 month to 24 months, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected. | 0 | 3.55 | 3 | 0 |
P carinii Pneumonia [description not available] | 0 | 3.8 | 4 | 0 |
Pneumonia, Pneumocystis A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis. | 0 | 3.8 | 4 | 0 |
Female Genital Diseases [description not available] | 0 | 1.96 | 1 | 0 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 1.96 | 1 | 0 |
Infections, Chlamydia [description not available] | 0 | 2.88 | 4 | 0 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 2.88 | 4 | 0 |
Nasopharyngitis Inflammation of the NASOPHARYNX, usually including its mucosa, related lymphoid structure, and glands. | 0 | 8.21 | 6 | 0 |
Dandy-Walker Complex [description not available] | 0 | 2.67 | 3 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 2.65 | 3 | 0 |
Vertigo An illusion of movement, either of the external world revolving around the individual or of the individual revolving in space. Vertigo may be associated with disorders of the inner ear (EAR, INNER); VESTIBULAR NERVE; BRAINSTEM; or CEREBRAL CORTEX. Lesions in the TEMPORAL LOBE and PARIETAL LOBE may be associated with FOCAL SEIZURES that may feature vertigo as an ictal manifestation. (From Adams et al., Principles of Neurology, 6th ed, pp300-1) | 0 | 2.65 | 3 | 0 |
Cochlear Hearing Loss [description not available] | 0 | 2.36 | 2 | 0 |
Middle Ear Effusion [description not available] | 0 | 1.96 | 1 | 0 |
Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. | 0 | 2.36 | 2 | 0 |
Otitis Media with Effusion Inflammation of the middle ear with a clear pale yellow-colored transudate. | 0 | 1.96 | 1 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 1.96 | 1 | 0 |
Oligodendroglioma A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655) | 0 | 1.96 | 1 | 0 |
Chloasma [description not available] | 0 | 1.96 | 1 | 0 |
Atrophy, Muscle [description not available] | 0 | 1.96 | 1 | 0 |
External Ophthalmoplegia [description not available] | 0 | 1.96 | 1 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 6.96 | 1 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 1.96 | 1 | 0 |
Diseases of Nasopharynx [description not available] | 0 | 2.37 | 2 | 0 |
Experimental Pneumococcal Meningitis [description not available] | 0 | 1.96 | 1 | 0 |
Infections, Pneumococcal [description not available] | 0 | 2.35 | 2 | 0 |
Meningitis, Pneumococcal An acute purulent infection of the meninges and subarachnoid space caused by Streptococcus pneumoniae, most prevalent in children and adults over the age of 60. This illness may be associated with OTITIS MEDIA; MASTOIDITIS; SINUSITIS; RESPIRATORY TRACT INFECTIONS; sickle cell disease (ANEMIA, SICKLE CELL); skull fractures; and other disorders. Clinical manifestations include FEVER; HEADACHE; neck stiffness; and somnolence followed by SEIZURES; focal neurologic deficits (notably DEAFNESS); and COMA. (From Miller et al., Merritt's Textbook of Neurology, 9th ed, p111) | 0 | 1.96 | 1 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 2.35 | 2 | 0 |
Bovine Diseases [description not available] | 0 | 2.65 | 3 | 0 |
Alcohol Related Neurodevelopmental Disorder [description not available] | 0 | 1.96 | 1 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 3.05 | 5 | 0 |
Bilharziasis [description not available] | 0 | 1.95 | 1 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 1.95 | 1 | 0 |
Schistosomiasis Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States. | 0 | 1.95 | 1 | 0 |
Esophageal Stricture [description not available] | 0 | 2.35 | 2 | 0 |
Cervical Dystonia A common form of DYSTONIA due to involuntary sustained or spasmodic, repetitive muscle contractions in the neck region. According to the position of the twisted neck and head, cervical dystonia can be categorized as torticollis, laterocollis, retrocollis, and a combination of these abnormal postures. | 0 | 2.35 | 2 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 2.35 | 2 | 0 |
Torticollis A symptom, not a disease, of a twisted neck. In most instances, the head is tipped toward one side and the chin rotated toward the other. The involuntary muscle contractions in the neck region of patients with torticollis can be due to congenital defects, trauma, inflammation, tumors, and neurological or other factors. | 0 | 2.35 | 2 | 0 |
Acathisia, Drug-Induced [description not available] | 0 | 3.82 | 4 | 0 |
Brachmann-De Lange Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
De Lange Syndrome A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231) | 0 | 1.98 | 1 | 0 |
Beckwith-Wiedemann Syndrome A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities. | 0 | 1.98 | 1 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 4.29 | 4 | 1 |
Cardiomyopathy, Dilated A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. | 0 | 4.29 | 4 | 1 |
Pleural Effusion Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself. | 0 | 2.66 | 3 | 0 |
Angina Pectoris with Normal Coronary Arteriogram [description not available] | 0 | 1.98 | 1 | 0 |
Dizzyness [description not available] | 0 | 3.76 | 2 | 1 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 3.76 | 2 | 1 |
Airway Hyper-Responsiveness [description not available] | 0 | 2.65 | 3 | 0 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 1.98 | 1 | 0 |
Encephalomyelitis A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature. | 0 | 6.98 | 1 | 0 |
Hydrophobia [description not available] | 0 | 2.37 | 2 | 0 |
Cancer of Esophagus [description not available] | 0 | 2.65 | 3 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 2.65 | 3 | 0 |
Glandular Fever [description not available] | 0 | 2.36 | 2 | 0 |
Infectious Mononucleosis A common, acute infection usually caused by the Epstein-Barr virus (HERPESVIRUS 4, HUMAN). There is an increase in mononuclear white blood cells and other atypical lymphocytes, generalized lymphadenopathy, splenomegaly, and occasionally hepatomegaly with hepatitis. | 0 | 2.36 | 2 | 0 |
Bilateral Nasal Obstruction [description not available] | 0 | 3.81 | 4 | 0 |
Nasal Obstruction Any hindrance to the passage of air into and out of the nose. The obstruction may be unilateral or bilateral, and may involve any part of the NASAL CAVITY. | 0 | 3.81 | 4 | 0 |
Congenital Stiff-Man Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Stiff-Person Syndrome A condition characterized by persistent spasms (SPASM) involving multiple muscles, primarily in the lower limbs and trunk. The illness tends to occur in the fourth to sixth decade of life, presenting with intermittent spasms that become continuous. Minor sensory stimuli, such as noise and light touch, precipitate severe spasms. Spasms do not occur during sleep and only rarely involve cranial muscles. Respiration may become impaired in advanced cases. (Adams et al., Principles of Neurology, 6th ed, p1492; Neurology 1998 Jul;51(1):85-93) | 0 | 1.98 | 1 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 2.37 | 2 | 0 |
Neurofibroma A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016) | 0 | 7.36 | 2 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 2.37 | 2 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 1.98 | 1 | 0 |
Cancer of Mediastinum [description not available] | 0 | 2.4 | 2 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 1.98 | 1 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 2.4 | 2 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 1.98 | 1 | 0 |
B Virus Infection [description not available] | 0 | 1.98 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 1.98 | 1 | 0 |
Asthmatic Crisis [description not available] | 0 | 2.9 | 1 | 0 |
Status Asthmaticus A sudden intense and continuous aggravation of a state of asthma, marked by dyspnea to the point of exhaustion and collapse and not responding to the usual therapeutic efforts. | 0 | 2.9 | 1 | 0 |
Infections, Listeria [description not available] | 0 | 2.36 | 2 | 0 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 1.98 | 1 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 2.38 | 2 | 0 |
Coronaviridae Infections Virus diseases caused by CORONAVIRIDAE. | 0 | 1.98 | 1 | 0 |
Aberrant Tissue [description not available] | 0 | 1.98 | 1 | 0 |
Microstomia A congenital defect in which the mouth is unusually small. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 1.98 | 1 | 0 |
Peripheral Nervous System Neoplasms Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1) | 0 | 1.98 | 1 | 0 |
Paroxysmal Reciprocal Tachycardia [description not available] | 0 | 3.05 | 5 | 0 |
Tachycardia, Paroxysmal Abnormally rapid heartbeats with sudden onset and cessation. | 0 | 3.05 | 5 | 0 |
Corynebacterium diphtheriae Infection [description not available] | 0 | 2.9 | 1 | 0 |
Diphtheria A localized infection of mucous membranes or skin caused by toxigenic strains of CORYNEBACTERIUM DIPHTHERIAE. It is characterized by the presence of a pseudomembrane at the site of infection. DIPHTHERIA TOXIN, produced by C. diphtheriae, can cause myocarditis, polyneuritis, and other systemic toxic effects. | 0 | 2.9 | 1 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 2.37 | 2 | 0 |
Macrostomia Greatly exaggerated width of the mouth, resulting from failure of union of the maxillary and mandibular processes, with extension of the oral orifice toward the ear. The defect may be unilateral or bilateral. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Craniofacial Dysarthrosis [description not available] | 0 | 1.98 | 1 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 1.98 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 4.28 | 4 | 1 |
Enlarged Spleen [description not available] | 0 | 3.79 | 2 | 1 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 2.37 | 2 | 0 |
Disseminated Intravascular Coagulation A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS. | 0 | 2.37 | 2 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 2.39 | 2 | 0 |
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 | 2.39 | 2 | 0 |
Injuries, Whiplash [description not available] | 0 | 1.98 | 1 | 0 |
Infantile Diarrhea [description not available] | 0 | 3.3 | 2 | 0 |
Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. | 0 | 3.3 | 2 | 0 |
Anomalous Ventricular Excitation Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
Wolff-Parkinson-White Syndrome A form of ventricular pre-excitation characterized by a short PR interval and a long QRS interval with a delta wave. In this syndrome, atrial impulses are abnormally conducted to the HEART VENTRICLES via an ACCESSORY CONDUCTING PATHWAY that is located between the wall of the right or left atria and the ventricles, also known as a BUNDLE OF KENT. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated protein kinase. | 0 | 1.99 | 1 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 4.07 | 3 | 1 |
Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). | 0 | 4.07 | 3 | 1 |
Drug Abuse, Intravenous [description not available] | 0 | 2.9 | 1 | 0 |
Sneezing The sudden, forceful, involuntary expulsion of air from the NOSE and MOUTH caused by irritation to the MUCOUS MEMBRANES of the upper RESPIRATORY TRACT. | 0 | 4.27 | 4 | 0 |
Teeth, Impacted [description not available] | 0 | 2.37 | 2 | 0 |
Liver Dysfunction [description not available] | 0 | 3.57 | 3 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 8.57 | 3 | 0 |
Eye Disorders [description not available] | 0 | 2.65 | 3 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 2.65 | 3 | 0 |
Goldblatt Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
Renal Artery Stenosis [description not available] | 0 | 1.99 | 1 | 0 |
Hypertension, Renovascular Hypertension due to RENAL ARTERY OBSTRUCTION or compression. | 0 | 1.99 | 1 | 0 |
Renal Artery Obstruction Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR). | 0 | 1.99 | 1 | 0 |
Urinary Retention Inability to empty the URINARY BLADDER with voiding (URINATION). | 0 | 2.91 | 1 | 0 |
Caprine Diseases [description not available] | 0 | 3.38 | 1 | 1 |
Carotid Artery Narrowing [description not available] | 0 | 1.99 | 1 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 1.99 | 1 | 0 |
Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in the ANTERIOR CEREBRAL ARTERY; MIDDLE CEREBRAL ARTERY; and POSTERIOR CEREBRAL ARTERY. | 0 | 1.99 | 1 | 0 |
Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp 822-3) | 0 | 1.99 | 1 | 0 |
Childhood Eating and Feeding Disorders [description not available] | 0 | 3.38 | 1 | 1 |
Autoimmune Diabetes [description not available] | 0 | 2.67 | 3 | 0 |
Acidosis, Diabetic [description not available] | 0 | 1.99 | 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 | 2.67 | 3 | 0 |
Diabetic Ketoacidosis A life-threatening complication of diabetes mellitus, primarily of TYPE 1 DIABETES MELLITUS with severe INSULIN deficiency and extreme HYPERGLYCEMIA. It is characterized by KETOSIS; DEHYDRATION; and depressed consciousness leading to COMA. | 0 | 1.99 | 1 | 0 |
Mast Cell Activation Disease [description not available] | 0 | 3.32 | 2 | 0 |
Mastocytosis A rare neoplastic disorder characterized by a clonal proliferation of MAST CELLS, associated with KIT-D816 mutations, and accompanied by aberrant mast cell activation. The abnormal increase of MAST CELLS may occur in only the skin (MASTOCYTOSIS, CUTANEOUS), in extracutaneous tissues involving multiple organs (MASTOCYTOSIS, SYSTEMIC), or in solid tumors (MASTOCYTOMA). | 0 | 8.32 | 2 | 0 |
Cancer of Larynx [description not available] | 0 | 2.66 | 3 | 0 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 2.66 | 3 | 0 |
Atherosclerotic Parkinsonism [description not available] | 0 | 1.99 | 1 | 0 |
Parkinson Disease, Secondary Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42) | 0 | 1.99 | 1 | 0 |
Chondrodystrophic Myotonia [description not available] | 0 | 1.99 | 1 | 0 |
Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | 0 | 2.66 | 3 | 0 |
Capillary Leak Syndrome A condition characterized by recurring episodes of fluid leaking from capillaries into extra-vascular compartments causing hematocrit to rise precipitously. If not treated, generalized vascular leak can lead to generalized EDEMA; SHOCK; cardiovascular collapse; and MULTIPLE ORGAN FAILURE. | 0 | 2.91 | 1 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.91 | 1 | 0 |
Leukemia, Lymphocytic, Chronic, B-Cell A chronic leukemia characterized by abnormal B-lymphocytes and often generalized lymphadenopathy. In patients presenting predominately with blood and bone marrow involvement it is called chronic lymphocytic leukemia (CLL); in those predominately with enlarged lymph nodes it is called small lymphocytic lymphoma. These terms represent spectrums of the same disease. | 0 | 2.91 | 1 | 0 |
Fatty Liver with Encephalopathy [description not available] | 0 | 2.37 | 2 | 0 |
Uremia A clinical syndrome associated with the retention of renal waste products or uremic toxins in the blood. It is usually the result of RENAL INSUFFICIENCY. Most uremic toxins are end products of protein or nitrogen CATABOLISM, such as UREA or CREATININE. Severe uremia can lead to multiple organ dysfunctions with a constellation of symptoms. | 0 | 2.91 | 1 | 0 |
Myxedema A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips. | 0 | 2.91 | 1 | 0 |
Abnormalities, Autosome [description not available] | 0 | 2.66 | 3 | 0 |
Anasarca [description not available] | 0 | 4.26 | 7 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 4.26 | 7 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 2 | 1 | 0 |
Facial Palsy [description not available] | 0 | 2 | 1 | 0 |
Epileptiform Neuralgia [description not available] | 0 | 2.37 | 2 | 0 |
Bernard Syndrome [description not available] | 0 | 2 | 1 | 0 |
Trigeminal Neuralgia A syndrome characterized by recurrent episodes of excruciating pain lasting several seconds or longer in the sensory distribution of the TRIGEMINAL NERVE. Pain may be initiated by stimulation of trigger points on the face, lips, or gums or by movement of facial muscles or chewing. Associated conditions include MULTIPLE SCLEROSIS, vascular anomalies, ANEURYSMS, and neoplasms. (Adams et al., Principles of Neurology, 6th ed, p187) | 0 | 2.37 | 2 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 2 | 1 | 0 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 2.37 | 2 | 0 |
Dermatitis, Irritant A non-allergic contact dermatitis caused by prolonged exposure to irritants and not explained by delayed hypersensitivity mechanisms. | 0 | 2 | 1 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 2.65 | 3 | 0 |
Prurigo A name applied to several itchy skin eruptions of unknown cause. The characteristic course is the formation of a dome-shaped papule with a small transient vesicle on top, followed by crusting over or lichenification. (From Dorland, 27th ed) | 0 | 2 | 1 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 2 | 1 | 0 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 2 | 1 | 0 |
Acid-Base Imbalance Disturbances in the ACID-BASE EQUILIBRIUM of the body. | 0 | 2.65 | 3 | 0 |
Xanthoma [description not available] | 0 | 2 | 1 | 0 |
Encephalitis Lethargica Type Parkinsonism [description not available] | 0 | 2 | 1 | 0 |
Parkinson Disease, Postencephalitic Parkinsonism following encephalitis, historically seen as a sequella of encephalitis lethargica (Von Economo Encephalitis). The early age of onset, the rapid progression of symptoms followed by stabilization, and the presence of a variety of other neurological disorders (e.g., sociopathic behavior; TICS; MUSCLE SPASMS; oculogyric crises; hyperphagia; and bizarre movements) distinguish this condition from primary PARKINSON DISEASE. Pathologic features include neuronal loss and gliosis concentrated in the MESENCEPHALON; SUBTHALAMUS; and HYPOTHALAMUS. (From Adams et al., Principles of Neurology, 6th ed, p754) | 0 | 2 | 1 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 2.36 | 2 | 0 |
Autosomal Hemophilia A [description not available] | 0 | 2 | 1 | 0 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 2 | 1 | 0 |
Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. | 0 | 2 | 1 | 0 |
Craniomandibular Diseases [description not available] | 0 | 2 | 1 | 0 |
Angle's Classification [description not available] | 0 | 2.4 | 2 | 0 |
Malocclusion Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982) | 0 | 2.4 | 2 | 0 |
Adrenal Cancer [description not available] | 0 | 2 | 1 | 0 |
Diabetic Coma A state of unconsciousness as a complication of diabetes mellitus. It occurs in cases of extreme HYPERGLYCEMIA or extreme HYPOGLYCEMIA as a complication of INSULIN therapy. | 0 | 2.37 | 2 | 0 |
Colicky Pain [description not available] | 0 | 2 | 1 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 2 | 1 | 0 |
Congenital Fissure of the Abdominal Cavity [description not available] | 0 | 2 | 1 | 0 |
Gastroschisis A congenital defect with major fissure in the ABDOMINAL WALL lateral to, but not at, the UMBILICUS. This results in the extrusion of VISCERA. Unlike OMPHALOCELE, herniated structures in gastroschisis are not covered by a sac or PERITONEUM. | 0 | 2 | 1 | 0 |
ENT Diseases [description not available] | 0 | 2 | 1 | 0 |
Microglossia [description not available] | 0 | 3.29 | 2 | 0 |
Apraxia [description not available] | 0 | 2.66 | 3 | 0 |
Aprosodia [description not available] | 0 | 2.65 | 3 | 0 |
Bulbar Palsy [description not available] | 0 | 2.38 | 2 | 0 |
Apraxias A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7) | 0 | 2.66 | 3 | 0 |
Urination Disorders Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE. | 0 | 2.37 | 2 | 0 |
Leukoma [description not available] | 0 | 3.39 | 1 | 1 |
alpha-L-Iduronidase Deficiency [description not available] | 0 | 3.76 | 2 | 1 |
Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | 0 | 3.39 | 1 | 1 |
Mucopolysaccharidosis I Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing. | 0 | 3.76 | 2 | 1 |
Compensatory Hyperinsulinemia A GLUCOSE-induced HYPERINSULINEMIA, a marker of insulin-resistant state. It is a mechanism to compensate for reduced sensitivity to insulin. | 0 | 2.37 | 2 | 0 |
Hyperinsulinism A syndrome with excessively high INSULIN levels in the BLOOD. It may cause HYPOGLYCEMIA. Etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor (INSULINOMA); autoantibodies against insulin (INSULIN ANTIBODIES); defective insulin receptor (INSULIN RESISTANCE); or overuse of exogenous insulin or HYPOGLYCEMIC AGENTS. | 0 | 2.37 | 2 | 0 |
Hyperdactyly [description not available] | 0 | 2.41 | 2 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 2 | 1 | 0 |
Germinoblastoma [description not available] | 0 | 2 | 1 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 2 | 1 | 0 |
Plasma Cell Tumor [description not available] | 0 | 2 | 1 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 2 | 1 | 0 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 2 | 1 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 2 | 1 | 0 |
Precursor Cell Lymphoblastic Leukemia-Lymphoma A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias. | 0 | 2 | 1 | 0 |
Amniotic Fluid Embolism [description not available] | 0 | 2 | 1 | 0 |
Blood Diseases [description not available] | 0 | 2.92 | 1 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 2.92 | 1 | 0 |
Chronic Fatigue and Immune Dysfunction Syndrome [description not available] | 0 | 2 | 1 | 0 |
Fatigue Syndrome, Chronic A syndrome characterized by persistent or recurrent fatigue, diffuse musculoskeletal pain, sleep disturbances, and subjective cognitive impairment of 6 months duration or longer. Symptoms are not caused by ongoing exertion; are not relieved by rest; and result in a substantial reduction of previous levels of occupational, educational, social, or personal activities. Minor alterations of immune, neuroendocrine, and autonomic function may be associated with this syndrome. There is also considerable overlap between this condition and FIBROMYALGIA. (From Semin Neurol 1998;18(2):237-42; Ann Intern Med 1994 Dec 15;121(12): 953-9) | 0 | 2 | 1 | 0 |
Cancer of Prostate [description not available] | 0 | 2 | 1 | 0 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 2 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 2 | 1 | 0 |
Sinus Tachycardia [description not available] | 0 | 2 | 1 | 0 |
Babesia Infection [description not available] | 0 | 2 | 1 | 0 |
Candida Infection [description not available] | 0 | 2.01 | 1 | 0 |
Candidiasis Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed) | 0 | 2.01 | 1 | 0 |
Coloboma Congenital anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation. | 0 | 2.01 | 1 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 2.65 | 3 | 0 |
Deficiency, Vitamin K [description not available] | 0 | 2.01 | 1 | 0 |
Vitamin K Deficiency A nutritional condition produced by a deficiency of VITAMIN K in the diet, characterized by an increased tendency to hemorrhage (HEMORRHAGIC DISORDERS). Such bleeding episodes may be particularly severe in newborn infants. (From Cecil Textbook of Medicine, 19th ed, p1182) | 0 | 2.01 | 1 | 0 |
Serotonin Syndrome An adverse drug interaction characterized by altered mental status, autonomic dysfunction, and neuromuscular abnormalities. It is most frequently caused by use of both serotonin reuptake inhibitors and monoamine oxidase inhibitors, leading to excess serotonin availability in the CNS at the serotonin 1A receptor. | 0 | 7.01 | 1 | 0 |
Hakim Syndrome [description not available] | 0 | 3.31 | 2 | 0 |
Entrapment Neuropathies [description not available] | 0 | 2.92 | 1 | 0 |
Arachnoid Cysts Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115) | 0 | 2.92 | 1 | 0 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 3.31 | 2 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 4.12 | 6 | 0 |
Cardiac Complex, Premature [description not available] | 0 | 4.84 | 8 | 1 |
Acute Myelogenous Leukemia [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Amnesia-Memory Loss [description not available] | 0 | 5.15 | 6 | 2 |
Amnesia Pathologic partial or complete loss of the ability to recall past experiences (AMNESIA, RETROGRADE) or to form new memories (AMNESIA, ANTEROGRADE). This condition may be of organic or psychologic origin. Organic forms of amnesia are usually associated with dysfunction of the DIENCEPHALON or HIPPOCAMPUS. (From Adams et al., Principles of Neurology, 6th ed, pp426-7) | 0 | 5.15 | 6 | 2 |
Cataleptic Attacks [description not available] | 0 | 3.78 | 4 | 0 |
Enuresis Involuntary discharge of URINE after expected age of completed development of urinary control. This can happen during the daytime (DIURNAL ENURESIS) while one is awake or during sleep (NOCTURNAL ENURESIS). Enuresis can be in children or in adults (as persistent primary enuresis and secondary adult-onset enuresis). | 0 | 3.56 | 3 | 0 |
Heroin Abuse [description not available] | 0 | 2.87 | 1 | 0 |
Heroin Dependence Strong dependence or addiction, both physiological and emotional, upon HEROIN. | 0 | 2.87 | 1 | 0 |
Anemia, Hemolytic, Acquired [description not available] | 0 | 4.57 | 4 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 1.95 | 1 | 0 |
Anemia, Hemolytic A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES). | 0 | 4.57 | 4 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 1.95 | 1 | 0 |
Water-Electrolyte Imbalance Disturbances in the body's WATER-ELECTROLYTE BALANCE. | 0 | 1.95 | 1 | 0 |
Hemorrhagic Disease of Newborn Neonatal nasogastric or intracranial hemorrhage caused by vitamin K deficiency. | 0 | 1.95 | 1 | 0 |
Alcohol Withdrawal Associated Autonomic Hyperactivity [description not available] | 0 | 1.95 | 1 | 0 |
Deficiency, Thiamine [description not available] | 0 | 3.27 | 2 | 0 |
Thiamine Deficiency A nutritional condition produced by a deficiency of THIAMINE in the diet, characterized by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, BERIBERI prevalence is very high. (From Cecil Textbook of Medicine, 19th ed, p1171) | 0 | 3.27 | 2 | 0 |
Akinetic Autism [description not available] | 0 | 1.95 | 1 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 2.35 | 2 | 0 |
Anus Prolapse [description not available] | 0 | 2.35 | 2 | 0 |
ADDH [description not available] | 0 | 3.27 | 2 | 0 |
Attention Deficit Disorder with Hyperactivity A behavior disorder originating in childhood in which the essential features are signs of developmentally inappropriate inattention, impulsivity, and hyperactivity. Although most individuals have symptoms of both inattention and hyperactivity-impulsivity, one or the other pattern may be predominant. The disorder is more frequent in males than females. Onset is in childhood. Symptoms often attenuate during late adolescence although a minority experience the full complement of symptoms into mid-adulthood. (From DSM-V) | 0 | 3.27 | 2 | 0 |
Allergy, Food [description not available] | 0 | 3.27 | 2 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 2.87 | 1 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 2.87 | 1 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 3.27 | 2 | 0 |
Acoustic Neuroma [description not available] | 0 | 1.95 | 1 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 1.95 | 1 | 0 |
Encephalitis, Inclusion Body, Measles [description not available] | 0 | 1.95 | 1 | 0 |
Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) | 0 | 1.95 | 1 | 0 |
Hysteria Historical term for a chronic, but fluctuating, disorder beginning in early life and characterized by recurrent and multiple somatic complaints not apparently due to physical illness. This diagnosis is not used in contemporary practice. | 0 | 4.11 | 6 | 0 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 1.95 | 1 | 0 |
Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, and sneezing. | 0 | 1.95 | 1 | 0 |
Varices [description not available] | 0 | 2.37 | 2 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 2.37 | 2 | 0 |
Ovine Diseases [description not available] | 0 | 2.36 | 2 | 0 |
Sore Throat [description not available] | 0 | 3.05 | 5 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 8.05 | 5 | 0 |
Sex Disorders [description not available] | 0 | 1.95 | 1 | 0 |
Sexual Dysfunction, Physiological Physiological disturbances in normal sexual performance in either the male or the female. | 0 | 1.95 | 1 | 0 |
Autolysis The spontaneous disintegration of tissues or cells by the action of their own autogenous enzymes. | 0 | 1.95 | 1 | 0 |
Bowel Incontinence [description not available] | 0 | 1.95 | 1 | 0 |
Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | 0 | 1.95 | 1 | 0 |
Cadaver A dead body, usually a human body. | 0 | 1.95 | 1 | 0 |
Haemophilus influenzae Meningitis Type B [description not available] | 0 | 1.95 | 1 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 1.95 | 1 | 0 |
Glycosuria The appearance of an abnormally large amount of GLUCOSE in the urine, such as more than 500 mg/day in adults. It can be due to HYPERGLYCEMIA or genetic defects in renal reabsorption (RENAL GLYCOSURIA). | 0 | 2.35 | 2 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 1.95 | 1 | 0 |
Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology. | 0 | 1.95 | 1 | 0 |
Deficiency, Magnesium [description not available] | 0 | 5.37 | 5 | 1 |
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 | 5.37 | 5 | 1 |
Cardiac Septal Defect [description not available] | 0 | 1.95 | 1 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 3.26 | 2 | 0 |
Polyuria Urination of a large volume of urine with an increase in urinary frequency, commonly seen in diabetes (DIABETES MELLITUS; DIABETES INSIPIDUS). | 0 | 1.95 | 1 | 0 |
Acetonemia [description not available] | 0 | 1.95 | 1 | 0 |
Beriberi, Cerebral [description not available] | 0 | 1.95 | 1 | 0 |
Hyperactivity, Motor [description not available] | 0 | 2.65 | 3 | 0 |
Placental Insufficiency Failure of the PLACENTA to deliver an adequate supply of nutrients and OXYGEN to the FETUS. | 0 | 1.95 | 1 | 0 |
Cleft Spine [description not available] | 0 | 2.64 | 3 | 0 |
Erythroblastosis Fetalis [description not available] | 0 | 3.78 | 4 | 0 |
Poultry Diseases Diseases of birds which are raised as a source of meat or eggs for human consumption and are usually found in barnyards, hatcheries, etc. The concept is differentiated from BIRD DISEASES which is for diseases of birds not considered poultry and usually found in zoos, parks, and the wild. | 0 | 1.95 | 1 | 0 |
Neoplasms, Skull [description not available] | 0 | 2.35 | 2 | 0 |
Paralysis, Legs [description not available] | 0 | 2.35 | 2 | 0 |
Paraplegia Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness. | 0 | 2.35 | 2 | 0 |
Benign Intracranial Hypertension [description not available] | 0 | 2.36 | 2 | 0 |
Pseudotumor Cerebri A condition marked by raised intracranial pressure and characterized clinically by HEADACHES; NAUSEA; PAPILLEDEMA, peripheral constriction of the visual fields, transient visual obscurations, and pulsatile TINNITUS. OBESITY is frequently associated with this condition, which primarily affects women between 20 and 44 years of age. Chronic PAPILLEDEMA may lead to optic nerve injury (see OPTIC NERVE DISEASES) and visual loss (see BLINDNESS). | 0 | 2.36 | 2 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 1.95 | 1 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 1.95 | 1 | 0 |
Kussmaul Aphasia [description not available] | 0 | 1.98 | 1 | 0 |
Vestibular Diseases Pathological processes of the VESTIBULAR LABYRINTH which contains part of the balancing apparatus. Patients with vestibular diseases show instability and are at risk of frequent falls. | 0 | 1.98 | 1 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Esophageal Spasm [description not available] | 0 | 1.98 | 1 | 0 |
HIV Coinfection [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Wounds, Stab Penetrating wounds caused by a pointed object. | 0 | 1.97 | 1 | 0 |
Cardiac Tamponade Compression of the heart by accumulated fluid (PERICARDIAL EFFUSION) or blood (HEMOPERICARDIUM) in the PERICARDIUM surrounding the heart. The affected cardiac functions and CARDIAC OUTPUT can range from minimal to total hemodynamic collapse. | 0 | 2.64 | 3 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 1.97 | 1 | 0 |
Abstinence Syndrome, Neonatal [description not available] | 0 | 2.38 | 2 | 0 |
Neonatal Abstinence Syndrome Fetal and neonatal addiction and withdrawal as a result of the mother's dependence on drugs during pregnancy. Withdrawal or abstinence symptoms develop shortly after birth. Symptoms exhibited are loud, high-pitched crying, sweating, yawning and gastrointestinal disturbances. | 0 | 2.38 | 2 | 0 |
Cardiac Neurosis [description not available] | 0 | 2.36 | 2 | 0 |
Diseases of Immune System [description not available] | 0 | 3.28 | 2 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 3.28 | 2 | 0 |
Ataxias, Hereditary [description not available] | 0 | 2.38 | 2 | 0 |
Envenomation, Snakebite [description not available] | 0 | 2.36 | 2 | 0 |
Compartment Syndromes Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the causes of increased pressure are TRAUMA, tight dressings, HEMORRHAGE, and exercise. Sequelae include nerve compression (NERVE COMPRESSION SYNDROMES); PARALYSIS; and ISCHEMIC CONTRACTURE. FASCIOTOMY is often used to decompress increased pressure and eliminate pain associated with compartment syndromes. | 0 | 1.97 | 1 | 0 |
Disgerminoma [description not available] | 0 | 2.89 | 1 | 0 |
Dysgerminoma A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646) | 0 | 2.89 | 1 | 0 |
Eaton-Lambert Myasthenic Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Lambert-Eaton Myasthenic Syndrome An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471) | 0 | 1.97 | 1 | 0 |
Atresia, Choanal [description not available] | 0 | 2.38 | 2 | 0 |
Dextro-Looped Transposition of the Great Arteries [description not available] | 0 | 2.36 | 2 | 0 |
Transposition of Great Vessels A congenital cardiovascular malformation in which the AORTA arises entirely from the RIGHT VENTRICLE, and the PULMONARY ARTERY arises from the LEFT VENTRICLE. Consequently, the pulmonary and the systemic circulations are parallel and not sequential, so that the venous return from the peripheral circulation is re-circulated by the right ventricle via aorta to the systemic circulation without being oxygenated in the lungs. This is a potentially lethal form of heart disease in newborns and infants. | 0 | 2.36 | 2 | 0 |
Hospital-Addiction Syndrome [description not available] | 0 | 3.22 | 6 | 0 |
Avian Diseases [description not available] | 0 | 1.97 | 1 | 0 |
Anankastic Personality [description not available] | 0 | 1.97 | 1 | 0 |
Obsessive-Compulsive Disorder An anxiety disorder characterized by recurrent, persistent obsessions or compulsions. Obsessions are the intrusive ideas, thoughts, or images that are experienced as senseless or repugnant. Compulsions are repetitive and seemingly purposeful behavior which the individual generally recognizes as senseless and from which the individual does not derive pleasure although it may provide a release from tension. | 0 | 1.97 | 1 | 0 |
Dejerine-Thomas Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 3.28 | 2 | 0 |
Infectious Myelitis [description not available] | 0 | 1.97 | 1 | 0 |
Demyelinative Myelitis [description not available] | 0 | 1.97 | 1 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 1.97 | 1 | 0 |
Lymphangioma A benign tumor resulting from a congenital malformation of the lymphatic system. Lymphangioendothelioma is a type of lymphangioma in which endothelial cells are the dominant component. | 0 | 1.97 | 1 | 0 |
Shock, Surgical A type of shock that occurs as a result of a surgical procedure. | 0 | 2.36 | 2 | 0 |
Bezoars Concretions of swallowed hair, fruit or vegetable fibers, or similar substances found in the alimentary canal. | 0 | 1.97 | 1 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 1.97 | 1 | 0 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 1.97 | 1 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 2.36 | 2 | 0 |
Arteriosclerosis Thickening and loss of elasticity of the walls of ARTERIES of all sizes. There are many forms classified by the types of lesions and arteries involved, such as ATHEROSCLEROSIS with fatty lesions in the ARTERIAL INTIMA of medium and large muscular arteries. | 0 | 3.56 | 3 | 0 |
Bile Duct Obstruction [description not available] | 0 | 2.37 | 2 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 2.37 | 2 | 0 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 1.97 | 1 | 0 |
Esophageal Fistula Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA. | 0 | 1.97 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 1.97 | 1 | 0 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 1.97 | 1 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 1.97 | 1 | 0 |
Bed Sores [description not available] | 0 | 2.88 | 1 | 0 |
Pressure Ulcer An ulceration caused by prolonged pressure on the SKIN and TISSUES when one stays in one position for a long period of time, such as lying in bed. The bony areas of the body are the most frequently affected sites which become ischemic (ISCHEMIA) under sustained and constant pressure. | 0 | 2.88 | 1 | 0 |
Burns, Inhalation Burns of the respiratory tract caused by heat or inhaled chemicals. | 0 | 2.88 | 1 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 2.65 | 3 | 0 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 0 | 1.97 | 1 | 0 |
Pulmonary Fibrosis A process in which normal lung tissues are progressively replaced by FIBROBLASTS and COLLAGEN causing an irreversible loss of the ability to transfer oxygen into the bloodstream via PULMONARY ALVEOLI. Patients show progressive DYSPNEA finally resulting in death. | 0 | 2.65 | 3 | 0 |
Gangliocytoma [description not available] | 0 | 1.97 | 1 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 2.35 | 2 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Impotence [description not available] | 0 | 2.88 | 1 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 2.88 | 1 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 1.96 | 1 | 0 |
Cancer of Nose [description not available] | 0 | 1.96 | 1 | 0 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Dermoid [description not available] | 0 | 1.96 | 1 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 1.96 | 1 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 1.96 | 1 | 0 |
Clerambault Syndrome [description not available] | 0 | 1.96 | 1 | 0 |
Clostridioides difficile Infection [description not available] | 0 | 1.94 | 1 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 2.35 | 2 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 1.94 | 1 | 0 |
Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. | 0 | 3.27 | 2 | 0 |
Gigantism The condition of accelerated and excessive GROWTH in children or adolescents who are exposed to excess HUMAN GROWTH HORMONE before the closure of EPIPHYSES. It is usually caused by somatotroph hyperplasia or a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. These patients are of abnormally tall stature, more than 3 standard deviations above normal mean height for age. | 0 | 1.95 | 1 | 0 |
Malabsorption Syndromes General term for a group of MALNUTRITION syndromes caused by failure of normal INTESTINAL ABSORPTION of nutrients. | 0 | 1.95 | 1 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 1.95 | 1 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 1.94 | 1 | 0 |
Hypoproteinemia A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. | 0 | 1.94 | 1 | 0 |
Arbovirus Infections Infections caused by arthropod-borne viruses, general or unspecified. | 0 | 1.95 | 1 | 0 |
Necrotizing Pyelonephritis [description not available] | 0 | 2.86 | 4 | 0 |
Pyelonephritis Inflammation of the KIDNEY involving the renal parenchyma (the NEPHRONS); KIDNEY PELVIS; and KIDNEY CALICES. It is characterized by ABDOMINAL PAIN; FEVER; NAUSEA; VOMITING; and occasionally DIARRHEA. | 0 | 2.86 | 4 | 0 |
Hypertension, Renal Persistent high BLOOD PRESSURE due to KIDNEY DISEASES, such as those involving the renal parenchyma, the renal vasculature, or tumors that secrete RENIN. | 0 | 1.94 | 1 | 0 |
Island Cell Tumor [description not available] | 0 | 1.95 | 1 | 0 |
Metastase [description not available] | 0 | 1.95 | 1 | 0 |
Cancer of Pancreas [description not available] | 0 | 1.95 | 1 | 0 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 1.95 | 1 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 1.95 | 1 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 1.95 | 1 | 0 |
Pulmonary Stenoses [description not available] | 0 | 1.95 | 1 | 0 |
Burns, Electric Burns produced by contact with electric current or from a sudden discharge of electricity. | 0 | 1.95 | 1 | 0 |
Anthracosilicosis A form of pneumoconiosis caused by inhalation of dust that contains both CARBON and crystalline SILICON DIOXIDE. These foreign matters induce fibrous nodule formation in the lung. | 0 | 6.95 | 1 | 0 |
Staphylococcal Pneumonia [description not available] | 0 | 1.95 | 1 | 0 |
Pneumonia, Staphylococcal Pneumonia caused by infections with bacteria of the genus STAPHYLOCOCCUS, usually with STAPHYLOCOCCUS AUREUS. | 0 | 1.95 | 1 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 2.35 | 2 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 2.35 | 2 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.35 | 2 | 0 |
Heart Septal Defects, Ventricular Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect. | 0 | 2.35 | 2 | 0 |
Arteriovenous Malformations Abnormal formation of blood vessels that shunt arterial blood directly into veins without passing through the CAPILLARIES. They usually are crooked, dilated, and with thick vessel walls. A common type is the congenital arteriovenous fistula. The lack of blood flow and oxygen in the capillaries can lead to tissue damage in the affected areas. | 0 | 2.86 | 1 | 0 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 2.86 | 1 | 0 |
Absence of Voice [description not available] | 0 | 2.64 | 3 | 0 |
Hepatitis, Infectious [description not available] | 0 | 2.86 | 1 | 0 |
Hepatitis A INFLAMMATION of the LIVER in humans caused by a member of the HEPATOVIRUS genus, HUMAN HEPATITIS A VIRUS. It can be transmitted through fecal contamination of food or water. | 0 | 2.86 | 1 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 2.86 | 1 | 0 |
Psychoses, Alcoholic A group of mental disorders associated with organic brain damage and caused by poisoning from alcohol. | 0 | 1.94 | 1 | 0 |
Placenta Praevia [description not available] | 0 | 2.35 | 2 | 0 |
Placenta Previa Abnormal placentation in which the PLACENTA implants in the lower segment of the UTERUS (the zone of dilation) and may cover part or all of the opening of the CERVIX. It is often associated with serious antepartum bleeding and PREMATURE LABOR. | 0 | 2.35 | 2 | 0 |
Enterocele An intestinal HERNIA. | 0 | 1.95 | 1 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 1.95 | 1 | 0 |
Hernia Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired. | 0 | 1.95 | 1 | 0 |
Fibromatosis [description not available] | 0 | 1.95 | 1 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 1.95 | 1 | 0 |
Air Sickness [description not available] | 0 | 1.95 | 1 | 0 |
Motion Sickness Disorder caused by motion. It includes sea sickness, train sickness, roller coaster rides, rocking chair, hammock swing, car sickness, air sickness, or SPACE MOTION SICKNESS. Symptoms include nausea, vomiting and/or dizziness. | 0 | 1.95 | 1 | 0 |
Claustrophobia [description not available] | 0 | 1.95 | 1 | 0 |
Phobic Disorders Anxiety disorders in which the essential feature is persistent and irrational fear of a specific object, activity, or situation that the individual feels compelled to avoid. The individual recognizes the fear as excessive or unreasonable. | 0 | 1.95 | 1 | 0 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 1.95 | 1 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 1.95 | 1 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 1.95 | 1 | 0 |
Chylopericardium [description not available] | 0 | 1.95 | 1 | 0 |
Pericardial Effusion Fluid accumulation within the PERICARDIUM. Serous effusions are associated with pericardial diseases. Hemopericardium is associated with trauma. Lipid-containing effusion (chylopericardium) results from leakage of THORACIC DUCT. Severe cases can lead to CARDIAC TAMPONADE. | 0 | 1.95 | 1 | 0 |
Cystic Echinococcosis [description not available] | 0 | 1.95 | 1 | 0 |
Leukocytopenia [description not available] | 0 | 1.95 | 1 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 1.95 | 1 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 1.94 | 1 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 1.94 | 1 | 0 |
Asthma, Cardiac [description not available] | 0 | 2.35 | 2 | 0 |
Pleural Diseases Diseases involving the PLEURA. | 0 | 1.94 | 1 | 0 |
Cancer of Pharynx [description not available] | 0 | 1.94 | 1 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 1.94 | 1 | 0 |
Myoglobinuria The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis. | 0 | 1.94 | 1 | 0 |
Abnormalities, Severe Teratoid Marked developmental anomalies of a fetus or infant. | 0 | 1.94 | 1 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 1.94 | 1 | 0 |
Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement. | 0 | 1.94 | 1 | 0 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 2.35 | 2 | 0 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 1.94 | 1 | 0 |
Splenic Rupture Rupture of the SPLEEN due to trauma or disease. | 0 | 1.94 | 1 | 0 |
Astasia-Abasia [description not available] | 0 | 1.94 | 1 | 0 |
Menopause The last menstrual period. Permanent cessation of menses (MENSTRUATION) is usually defined after 6 to 12 months of AMENORRHEA in a woman over 45 years of age. In the United States, menopause generally occurs in women between 48 and 55 years of age. | 0 | 1.94 | 1 | 0 |
Inner Ear Disease [description not available] | 0 | 1.94 | 1 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 1.94 | 1 | 0 |
Hives [description not available] | 0 | 1.94 | 1 | 0 |
Urticaria A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress. | 0 | 1.94 | 1 | 0 |
Listeria Cerebritis [description not available] | 0 | 1.94 | 1 | 0 |
Polyradiculitis [description not available] | 0 | 1.94 | 1 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 1.94 | 1 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 1.94 | 1 | 0 |
Peptic Ulcer Ulcer that occurs in the regions of the GASTROINTESTINAL TRACT which come into contact with GASTRIC JUICE containing PEPSIN and GASTRIC ACID. It occurs when there are defects in the MUCOSA barrier. The common forms of peptic ulcers are associated with HELICOBACTER PYLORI and the consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 1.94 | 1 | 0 |
Endometrial Diseases [description not available] | 0 | 1.94 | 1 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 1.94 | 1 | 0 |
Dominant Hereditary Sensory Neuropathy, Type III [description not available] | 0 | 2.35 | 2 | 0 |
Dysautonomia, Familial An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4) | 0 | 2.35 | 2 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 1.94 | 1 | 0 |
Crisis, Thyrotoxic [description not available] | 0 | 1.94 | 1 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 1.94 | 1 | 0 |
Amyotrophic Neuralgia [description not available] | 0 | 1.94 | 1 | 0 |
Brachial Plexus Neuritis A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) | 0 | 1.94 | 1 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 1.94 | 1 | 0 |
Familial Mediterranean Fever A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene. | 0 | 1.94 | 1 | 0 |
Hematuria Presence of blood in the urine. | 0 | 1.94 | 1 | 0 |
Acrodynia A condition seen primarily in childhood, most often resulting from chronic exposure to MERCURY COMPOUNDS which may result in encephalopathy and POLYNEUROPATHY. Clinical features include pain, swelling and pinkish discoloration of the fingers and toes, weakness in the extremities, extreme irritability, HYPERESTHESIA, and alterations in level of consciousness. (From Menkes, Textbook of Child Neurology, 5th ed, p603) | 0 | 1.94 | 1 | 0 |
Gas Poisoning Poisoning that results from exposure to gases such as CARBON MONOXIDE; NOBLE GASES; OXYGEN; or NATURAL GAS. | 0 | 1.94 | 1 | 0 |
Dermatoses [description not available] | 0 | 2.35 | 2 | 0 |
Bone Diseases Diseases of BONES. | 0 | 1.94 | 1 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 2.35 | 2 | 0 |
Coarctation of Aorta [description not available] | 0 | 2.35 | 2 | 0 |
Aortic Coarctation A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion. | 0 | 2.35 | 2 | 0 |
Choked Disk [description not available] | 0 | 1.94 | 1 | 0 |
Papilledema Swelling of the OPTIC DISK, usually in association with increased intracranial pressure, characterized by hyperemia, blurring of the disk margins, microhemorrhages, blind spot enlargement, and engorgement of retinal veins. Chronic papilledema may cause OPTIC ATROPHY and visual loss. (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p175) | 0 | 1.94 | 1 | 0 |
Cramp [description not available] | 0 | 1.94 | 1 | 0 |
Muscle Cramp A sustained and usually painful contraction of muscle fibers. This may occur as an isolated phenomenon or as a manifestation of an underlying disease process (e.g., UREMIA; HYPOTHYROIDISM; MOTOR NEURON DISEASE; etc.). (From Adams et al., Principles of Neurology, 6th ed, p1398) | 0 | 1.94 | 1 | 0 |
Uterine Prolapse Downward displacement of the UTERUS. It is classified in various degrees: in the first degree the UTERINE CERVIX is within the vaginal orifice; in the second degree the cervix is outside the orifice; in the third degree the entire uterus is outside the orifice. | 0 | 1.94 | 1 | 0 |
Dental Enamel Hypoplasia An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors. | 0 | 1.94 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 1.94 | 1 | 0 |
Cancer of Cervix [description not available] | 0 | 1.94 | 1 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 1.94 | 1 | 0 |
Atypical Lipoma [description not available] | 0 | 1.94 | 1 | 0 |
Lipoma A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule. | 0 | 1.94 | 1 | 0 |
Gastric Dilatation Abnormal distention of the STOMACH due to accumulation of gastric contents that may reach 10 to 15 liters. Gastric dilatation may be the result of GASTRIC OUTLET OBSTRUCTION; ILEUS; GASTROPARESIS; or denervation. | 0 | 1.94 | 1 | 0 |
Tuberculosis, Female Genital MYCOBACTERIUM infections of the female reproductive tract (GENITALIA, FEMALE). | 0 | 1.94 | 1 | 0 |
As If Personality [description not available] | 0 | 1.94 | 1 | 0 |