| D007046 |
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. |
Hysterical Neuroses,Neuroses, Hysterical |
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| D002648 |
Child |
A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. |
Children |
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| D003291 |
Conversion Disorder |
A disorder whose predominant feature is a loss or alteration in physical functioning that suggests a physical disorder but that is actually a direct expression of a psychological conflict or need. |
Astasia-Abasia,Conversion Neurosis,Functional Movement Disorder,Functional Neurological Disorder,Hysteria, Conversion,Conversion Reaction,Astasia Abasia,Conversion Disorders,Conversion Hysteria,Conversion Neuroses,Disorder, Functional Movement,Disorder, Functional Neurological,Functional Movement Disorders,Functional Neurological Disorders,Movement Disorder, Functional,Movement Disorders, Functional,Neurological Disorder, Functional,Neurological Disorders, Functional,Neuroses, Conversion,Neurosis, Conversion |
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| D004422 |
Dystonia Musculorum Deformans |
A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078) |
Childhood Torsion Disease,Idiopathic Torsion Dystonia,Oppenheim-Ziehen Disease,Progressive Torsion Spasm,Torsion Dystonia,Dystonia Deformans Musculorum,Dystonia Deformans Progressiva,Torsion Disease of Childhood,Dystonia, Idiopathic Torsion,Dystonias, Idiopathic Torsion,Dystonias, Torsion,Idiopathic Torsion Dystonias,Oppenheim Ziehen Disease,Spasm, Progressive Torsion,Torsion Disease, Childhood,Torsion Dystonia, Idiopathic,Torsion Spasm, Progressive |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D014282 |
Trihexyphenidyl |
One of the centrally acting MUSCARINIC ANTAGONISTS used for treatment of PARKINSONIAN DISORDERS and drug-induced extrapyramidal movement disorders and as an antispasmodic. |
Benzhexol,Apo-Trihex,Artane,Cyclodol,Hipokinon,Parkinane,Parkopan,Trihexane,Trihexidyl Hydrochloride,Trihexyphenidyl Hydrochloride,Trihexyphenidyl Hydrochloride Elixir,Apo Trihex,ApoTrihex |
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| D020821 |
Dystonic Disorders |
Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset. |
Familial Dystonia,Focal Dystonia,Pseudodystonia,Writer's Cramp,Adult-Onset Dystonias,Adult-Onset Idiopathic Focal Dystonias,Adult-Onset Idiopathic Torsion Dystonias,Autosomal Dominant Familial Dystonia,Autosomal Recessive Familial Dystonia,Childhood Onset Dystonias,Dystonia Disorders,Dystonia, Hereditary,Dystonia, Primary,Dystonia, Psychogenic,Dystonia, Secondary,Dystonias, Sporadic,Familial Dystonia, Autosomal Dominant,Familial Dystonia, Autosomal Recessive,Familial Dystonia, Idiopathic,Secondary Dystonia,Adult Onset Dystonias,Adult Onset Idiopathic Focal Dystonias,Adult Onset Idiopathic Torsion Dystonias,Adult-Onset Dystonia,Childhood Onset Dystonia,Dystonia Disorder,Dystonia, Adult-Onset,Dystonia, Childhood Onset,Dystonia, Familial,Dystonia, Focal,Dystonia, Idiopathic Familial,Dystonia, Sporadic,Dystonias, Adult-Onset,Dystonias, Childhood Onset,Dystonias, Familial,Dystonias, Focal,Dystonias, Hereditary,Dystonias, Idiopathic Familial,Dystonias, Primary,Dystonias, Psychogenic,Dystonias, Secondary,Dystonic Disorder,Familial Dystonias,Familial Dystonias, Idiopathic,Focal Dystonias,Hereditary Dystonia,Hereditary Dystonias,Idiopathic Familial Dystonia,Idiopathic Familial Dystonias,Primary Dystonia,Primary Dystonias,Pseudodystonias,Psychogenic Dystonia,Psychogenic Dystonias,Secondary Dystonias,Sporadic Dystonia,Sporadic Dystonias,Writer Cramp,Writers Cramp |
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| D040181 |
Genetic Diseases, X-Linked |
Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases. |
X-Linked Genetic Diseases,Genetic Diseases, X-Chromosome Linked,Disease, X-Linked Genetic,Diseases, X-Linked Genetic,Genetic Disease, X-Linked,Genetic Diseases, X Chromosome Linked,Genetic Diseases, X Linked,X Linked Genetic Diseases,X-Linked Genetic Disease |
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