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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
C05.651.534.500 Muscular Dystrophies .
C05.651.534.500.300 Muscular Dystrophy, Duchenne .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.898 Tourette Syndrome .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.163.100.362.775 Pelizaeus-Merzbacher Disease .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.775 Pelizaeus-Merzbacher Disease .
C10.228.662 Movement Disorders .
C10.228.662.825 Tic Disorders .
C10.228.662.825.800 Tourette Syndrome .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.775 Pelizaeus-Merzbacher Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.850 Tourette Syndrome .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C10.668.491.175.500 Muscular Dystrophies .
C10.668.491.175.500.300 Muscular Dystrophy, Duchenne .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.562 Muscular Dystrophy, Duchenne .
C16.320.322.906 Pelizaeus-Merzbacher Disease .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.820 Tourette Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C16.320.565.189.362.775 Pelizaeus-Merzbacher Disease .
C16.320.577 Muscular Dystrophies .
C16.320.577.300 Muscular Dystrophy, Duchenne .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.132.100.362.775 Pelizaeus-Merzbacher Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.648.189.362.775 Pelizaeus-Merzbacher Disease .
F03 Mental Disorders .
F03.625 Neurodevelopmental Disorders .
F03.625.094 Attention Deficit and Disruptive Behavior Disorders .
F03.625.094.150 Attention Deficit Disorder with Hyperactivity .
F03.625.094.300 Conduct Disorder .
F03.625.968 Schizophrenia, Childhood .
F03.625.992 Tic Disorders .
F03.625.992.850 Tourette Syndrome .
F03.675 Personality Disorders .
F03.675.050 Antisocial Personality Disorder .
F03.675.100 Borderline Personality Disorder .
F03.675.200 Dependent Personality Disorder .
N05 Health Care Quality, Access, and Evaluation .
N05.715 Quality of Health Care .
N05.715.350 Epidemiologic Factors .
N05.715.350.075 Age Factors .
N05.715.350.075.100 Age of Onset .
N06 Environment and Public Health .
N06.850 Public Health .
N06.850.490 Epidemiologic Factors .
N06.850.490.250 Age Factors .
N06.850.490.250.100 Age of Onset .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Antisocial Personality Disorder .
Antisocial Personality .
Antisocial Personalities .
Antisocial Personality Disorders .
Behavior, Dyssocial .
Behaviors, Dyssocial .
Disorder, Antisocial Personality .
Disorders, Antisocial Personality .
Dyssocial Behaviors .
Personalities, Antisocial .
Personalities, Psychopathic .
Personalities, Sociopathic .
Personality Disorders, Antisocial .
Personality, Antisocial .
Personality, Psychopathic .
Personality, Sociopathic .
Psychopathic Personalities .
Sociopathic Personalities .
Dyssocial Behavior .
Personality Disorder, Antisocial .
Psychopathic Personality .
Sociopathic Personality .
A personality disorder whose essential feature is a pervasive pattern of disregard for, and violation of, the rights of others that begins in childhood or early adolescence and continues into adulthood. The individual must be at least age 18 and must have a history of some symptoms of CONDUCT DISORDER before age 15. (From DSM-IV, 1994) .
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2338035
 
Dependent Personality Disorder .
Dependent Personality Disorders .
Disorder, Dependent Personality .
Passive Dependent Personality .
Personality, Passive-Dependent .
Passive-Dependent Personality .
Personality Disorder, Dependent .
A personality disorder characterized by a pervasive and excessive need to be taken care of that leads to submissive and clinging behavior and fears of separation, beginning by early adulthood and present in a variety of contexts. (From DSM-IV, 1994) .
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Borderline Personality Disorder .
Disorder, Borderline Personality .
Borderline Personality Disorders .
Disorders, Borderline Personality .
Personality Disorders, Borderline .
Personality Disorder, Borderline .
A personality disorder marked by a pattern of instability of interpersonal relationships, self-image, and affects, and marked impulsivity beginning by early adulthood and present in a variety of contexts. (DSM-IV) .
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Tourette Syndrome .
Chronic Motor and Vocal Tic Disorder .
Combined Multiple Motor and Vocal Tic Disorder .
Combined Vocal and Multiple Motor Tic Disorder .
Gilles De La Tourette's Syndrome .
Gilles de la Tourette Syndrome .
Multiple Motor and Vocal Tic Disorder, Combined .
Tourette Disease .
Tourette Disorder .
Tourette's Disease .
Tourette's Disorder .
Tourette's Syndrome .
Syndrome, Tourette .
Tourettes Disease .
Tourettes Disorder .
Tourettes Syndrome .
Gilles de la Tourette's Disease .
Tic Disorder, Combined Vocal and Multiple Motor .
TOURETTE'S DISORDER .
A neuropsychological disorder related to alterations in DOPAMINE metabolism and neurotransmission involving frontal-subcortical neuronal circuits. Both multiple motor and one or more vocal tics need to be present with TICS occurring many times a day, nearly daily, over a period of more than one year. The onset is before age 18 and the disturbance is not due to direct physiological effects of a substance or a another medical condition. The disturbance causes marked distress or significant impairment in social, occupational, or other important areas of functioning. (From DSM-IV, 1994; Neurol Clin 1997 May;15(2):357-79) .
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1073924
 
Conduct Disorder .
Conduct Disorders .
A repetitive and persistent pattern of behavior in which the basic rights of others or major age-appropriate societal norms or rules are violated. These behaviors include aggressive conduct that causes or threatens physical harm to other people or animals, nonaggressive conduct that causes property loss or damage, deceitfulness or theft, and serious violations of rules. The onset is before age 18. (From DSM-IV, 1994) .
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Age of Onset .
Age-at-Onset .
Age at Onset .
Onset Age .
The age, developmental stage, or period of life at which a disease or the initial symptoms or manifestations of a disease appear in an individual. .
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Attention Deficit Disorder with Hyperactivity .
ADDH 1012 .
Attention Deficit Disorders with Hyperactivity .
Attention Deficit Hyperactivity Disorders .
Attention Deficit-Hyperactivity Disorder .
Attention Deficit Disorders .
Attention Deficit-Hyperactivity Disorders .
Deficit Disorder, Attention .
Deficit Disorders, Attention .
Deficit-Hyperactivity Disorder, Attention .
Deficit-Hyperactivity Disorders, Attention .
Disorder, Attention Deficit .
Disorder, Attention Deficit-Hyperactivity .
Disorders, Attention Deficit .
Disorders, Attention Deficit-Hyperactivity .
Dysfunction, Minimal Brain .
Syndromes, Hyperkinetic .
Brain Dysfunction, Minimal .
Hyperkinetic Syndrome .
Minimal Brain Dysfunction .
Attention Deficit Hyperactivity Disorder .
Attention Deficit Disorder .
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) .
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79724412
 
Muscular Dystrophy, Duchenne .
Becker's Muscular Dystrophy .
Cardiomyopathy, Dilated, 3B .
Cardiomyopathy, Dilated, X-Linked .
Childhood Muscular Dystrophy, Pseudohypertrophic .
Childhood Pseudohypertrophic Muscular Dystrophy .
Duchenne and Becker Muscular Dystrophy .
Duchenne-Becker Muscular Dystrophy .
Duchenne-Type Progressive Muscular Dystrophy .
Muscular Dystrophy Pseudohypertrophic Progressive, Becker Type .
Muscular Dystrophy, Becker Type .
Muscular Dystrophy, Childhood, Pseudohypertrophic .
Muscular Dystrophy, Duchenne Type .
Muscular Dystrophy, Duchenne and Becker Types .
Muscular Dystrophy, Pseudohypertrophic Progressive, Becker Type .
Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type .
Muscular Dystrophy, Pseudohypertrophic, Childhood .
Progressive Muscular Dystrophy, Duchenne Type .
Pseudohypertrophic Childhood Muscular Dystrophy .
Pseudohypertrophic Muscular Dystrophy, Childhood .
Duchenne Becker Muscular Dystrophy .
Duchenne Type Progressive Muscular Dystrophy .
Muscular Dystrophy, Becker's .
Muscular Dystrophy, Duchenne-Becker .
Pseudohypertrophic Muscular Dystrophy .
Becker Muscular Dystrophy .
Duchenne Muscular Dystrophy .
Muscular Dystrophy, Becker .
Muscular Dystrophy, Pseudohypertrophic .
An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) .
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1584262
 
Schizophrenia, Childhood .
Childhood-Onset Schizophrenia .
Childhood Onset Schizophrenia .
Schizophrenia, Childhood-Onset .
Childhood Schizophrenia .
An obsolete concept, historically used for childhood mental disorders thought to be a form of schizophrenia. It was in earlier versions of DSM but is now included within the broad concept of PERVASIVE DEVELOPMENT DISORDERS. .
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Pelizaeus-Merzbacher Disease .
Adult Pelizaeus-Merzbacher Disease .
Atypical Pelizaeus-Merzbacher Disease .
Classic Pelizaeus-Merzbacher Disease .
Leukodystrophy, Hypomyelinating, 1 .
Pelizaeus-Merzbacher Brain Sclerosis .
Pelizaeus-Merzbacher Disease, Adult .
Pelizaeus-Merzbacher Disease, Atypical .
Pelizaeus-Merzbacher Disease, Classic .
Pelizaeus-Merzbacher Disease, Transitional .
Pelizaeus-Merzbacher Sclerosis, Brain .
Transitional Pelizaeus-Merzbacher Disease .
Adult Pelizaeus Merzbacher Disease .
Atypical Pelizaeus Merzbacher Disease .
Brain Pelizaeus-Merzbacher Sclerosis .
Brain Sclerosis, Pelizaeus-Merzbacher .
Classic Pelizaeus Merzbacher Disease .
Cockayne Pelizaeus Merzbacher Disease .
Pelizaeus Merzbacher Brain Sclerosis .
Pelizaeus Merzbacher Disease .
Pelizaeus Merzbacher Disease, Adult .
Pelizaeus Merzbacher Disease, Atypical .
Pelizaeus Merzbacher Disease, Classic .
Pelizaeus Merzbacher Disease, Transitional .
Pelizaeus Merzbacher Sclerosis, Brain .
Transitional Pelizaeus Merzbacher Disease .
Cockayne-Pelizaeus-Merzbacher Disease .
A rare, slowly progressive disorder of myelin formation. Subtypes are referred to as classic, congenital, transitional, and adult forms of this disease. The classic form is X-chromosome linked, has its onset in infancy and is associated with a mutation of the proteolipid protein gene. Clinical manifestations include TREMOR, spasmus nutans, roving eye movements, ATAXIA, spasticity, and NYSTAGMUS, CONGENITAL. Death occurs by the third decade of life. The congenital form has similar characteristics but presents early in infancy and features rapid disease progression. Transitional and adult subtypes have a later onset and less severe symptomatology. Pathologic features include patchy areas of demyelination with preservation of perivascular islands (trigoid appearance). (From Menkes, Textbook of Child Neurology, 5th ed, p190) .
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