|
Fluorescein
|
D02.455.426.779.347.390 |
|
|
Lysine Carboxypeptidase
|
D08.811.277.656.675.555.750 |
|
|
Reed-Sternberg Cells
|
D016539 |
[Large cells, usually multinucleate, whose presence is a common histologic characteristic of classical HODGKIN DISEASE.
] |
|
Oculocerebrorenal Syndrome
|
C18.452.648.189.640 |
|
|
Polyethylene Terephthalates
|
J01.637.051.720.728.764 |
|
|
Gangliosidosis, GM1
|
D016537 |
[An autosomal recessive neurodegenerative disorder caused by the absence or deficiency of BETA-GALACTOSIDASE. It is characterized by intralysosomal accumulation of G(M1) GANGLIOSIDE and oligosaccharides, primarily in neurons of the central nervous system. The infantile form is characterized by MUSCLE HYPOTONIA, poor psychomotor development, HIRSUTISM, hepatosplenomegaly, and facial abnormalities. The juvenile form features HYPERACUSIS; SEIZURES; and psychomotor retardation. The adult form features progressive DEMENTIA; ATAXIA; and MUSCLE SPASTICITY. (From Menkes, Textbook of Child Neurology, 5th ed, pp96-7)
] |
|
Mucopolysaccharidosis VII
|
D016538 |
[Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase.
] |
|
Friedreich Ataxia
|
C18.452.660.300 |
|
|
Medical Order Entry Systems
|
N04.452.442.452.452.500 |
|
|
Tracheoesophageal Fistula
|
C08.702.750 |
|
|
Cobicistat
|
D02.886.675.182 |
|
|
Mucopolysaccharidosis II
|
D016532 |
[Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.
] |
|
Dasatinib
|
D02.886.675.184 |
|
|
Orthopedic Nursing
|
D016530 |
[The specialty or practice of nursing in the care of the orthopedic patient.
] |
|
Bronchial Hyperreactivity
|
D016535 |
[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.
] |
|
Competitive Medical Plans
|
D016536 |
[Alternative health care delivery mechanisms, such as PREFERRED PROVIDER ORGANIZATIONS or other health insurance services or prepaid plans (other than HEALTH MAINTENANCE ORGANIZATIONS), that meet Medicare qualifications for a risk-sharing contract. (From Facts on File Dictionary of Health Care Management, 1988)
] |
|
Mycological Typing Techniques
|
D016533 |
[Procedures for identifying types and strains of fungi.
] |
|
Dithiazanine
|
D02.886.675.188 |
|
|
Cardiac Output, High
|
D016534 |
[A state of elevated cardiac output due to conditions of either increased hemodynamic demand or reduced cardiac oxygen output. These conditions may include ANEMIA; ARTERIOVENOUS FISTULA; THYROTOXICOSIS; PREGNANCY; EXERCISE; FEVER; and HYPOXIA. In time, compensatory changes of the heart can lead to pathological form of high cardiac output and eventual HEART FAILURE.
] |
|
Leptospira
|
B03.851.475.475 |
|
