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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.545 Huntington Disease .
C10.228.140.380 Dementia .
C10.228.140.380.278 Huntington Disease .
C10.228.662 Movement Disorders .
C10.228.662.262 Dyskinesias .
C10.228.662.262.249 Chorea .
C10.228.662.262.249.750 Huntington Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.497 Huntington Disease .
C10.597 Neurologic Manifestations .
C10.597.350 Dyskinesias .
C10.597.350.250 Chorea .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.430 Huntington Disease .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.350 Dyskinesias .
C23.888.592.350.250 Chorea .
F03 Mental Disorders .
F03.615 Neurocognitive Disorders .
F03.615.250 Cognition Disorders .
F03.615.250.400 Huntington Disease .
F03.615.400 Dementia .
F03.615.400.390 Huntington Disease .
G05 Genetic Phenomena .
G05.390 Heredity .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Heredity .
The transmission of traits encoded in GENES from parent to offspring. .
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/genetics .
/heredity .
Used for mechanisms of heredity and the genetics of organisms, for the genetic basis of normal and pathologic states, and for the genetic aspects of endogenous chemicals. It includes biochemical and molecular influence on genetic material. .
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Genetic Diseases, Inborn .
Genetic Diseases .
Genetic Disorders .
Hereditary Disease .
Inborn Genetic Diseases .
Single-Gene Defects .
Defect, Single-Gene .
Defects, Single-Gene .
Disease, Genetic .
Disease, Hereditary .
Disease, Inborn Genetic .
Diseases, Genetic .
Diseases, Hereditary .
Diseases, Inborn Genetic .
Disorder, Genetic .
Disorders, Genetic .
Genetic Disease .
Genetic Disease, Inborn .
Genetic Disorder .
Inborn Genetic Disease .
Single Gene Defects .
Single-Gene Defect .
Hereditary Diseases .
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. .
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Chorea .
Chorea Disorders .
Chorea Syndromes .
Chorea, Benign Hereditary .
Chorea, Chronic Progressive .
Chorea, Rheumatic .
Chorea, Senile .
Chorea, Sydenham .
Choreatic Syndromes .
Choreic Movement .
Dyskinesias, Paroxysmal .
Hereditary Chorea .
Hereditary Progressive Chorea Without Dementia .
Paroxysmal Dyskinesias .
Rheumatic Chorea .
Senile Chorea .
St. Vitus's Dance .
Sydenham Chorea .
Sydenham's Chorea .
Benign Hereditary Chorea .
Benign Hereditary Choreas .
Chorea Disorder .
Chorea Syndrome .
Chorea, Hereditary .
Chorea, Sydenham's .
Choreas .
Choreas, Benign Hereditary .
Choreas, Chronic Progressive .
Choreas, Hereditary .
Choreas, Rheumatic .
Choreas, Senile .
Choreas, Sydenham .
Choreatic Disorder .
Choreatic Syndrome .
Choreic Movements .
Choreiform Movements .
Chronic Progressive Chorea .
Chronic Progressive Choreas .
Disorder, Chorea .
Disorder, Choreatic .
Disorders, Chorea .
Disorders, Choreatic .
Dyskinesia, Paroxysmal .
Hereditary Chorea, Benign .
Hereditary Choreas .
Hereditary Choreas, Benign .
Movement, Choreic .
Movement, Choreiform .
Movements, Choreic .
Movements, Choreiform .
Paroxysmal Dyskinesia .
Progressive Chorea, Chronic .
Progressive Choreas, Chronic .
Rheumatic Choreas .
Senile Choreas .
St. Vitus Dance .
St. Vitus's Dances .
St. Vituss Dance .
Sydenham Choreas .
Sydenhams Chorea .
Syndrome, Chorea .
Syndrome, Choreatic .
Syndromes, Chorea .
Syndromes, Choreatic .
Choreatic Disorders .
Choreiform Movement .
Chorea, Benign Hereditary .
Chorea, Rheumatic .
Chorea, Senile .
Chorea, Sydenham .
Dyskinesias, Paroxysmal .
Paroxysmal Dyskinesias .
Senile Chorea .
Sydenham Chorea .
Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES. .
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Huntington Disease .
Akinetic-Rigid Variant of Huntington Disease .
Chorea, Chronic Progressive Hereditary (Huntington) .
Chronic Progressive Hereditary Chorea (Huntington) .
Huntington Chronic Progressive Hereditary Chorea .
Huntington Disease, Akinetic-Rigid Variant .
Huntington Disease, Juvenile .
Huntington Disease, Juvenile-Onset .
Huntington Disease, Late Onset .
Huntington's Chorea .
Huntington's Disease .
Juvenile-Onset Huntington Disease .
Late-Onset Huntington Disease .
Progressive Chorea, Chronic Hereditary (Huntington) .
Progressive Chorea, Hereditary, Chronic (Huntington) .
Akinetic Rigid Variant of Huntington Disease .
Chorea, Huntington .
Chorea, Huntington's .
Huntington Disease, Akinetic Rigid Variant .
Huntington Disease, Juvenile Onset .
Huntington Disease, Late-Onset .
Juvenile Onset Huntington Disease .
Late Onset Huntington Disease .
Huntington Chorea .
Juvenile Huntington Disease .
CHOREA, HEREDITARY .
HUNTINGTON'S 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) .
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