Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency,Dystonia 11, Myoclonic,Somatoform Disorder,Aromatic L-Amino Acid Decarboxylase Deficiency,Movement Disease,Hyperphenylalaninemia,Isolated Dystonia,Tetrahydrobiopterin Deficiency,Leber Plus Disease,Choreatic Disease,Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia,Hereditary Dystonia,Blepharospasm,Sleep Disorder,Dystonia,Gliosarcoma,Parkinson Disease, Late-Onset,Pheochromocytoma,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Cutis Laxa, Autosomal Dominant 1,Hermansky-Pudlak Syndrome,Hyperphenylalaninemia, Bh4-Deficient, B,Dystonia, Dopa-Responsive,Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency,Dystonia 12,Segawa Syndrome, Autosomal Recessive,Cutis Laxa, Autosomal Dominant 2,Focal Dystonia,Multifocal Dystonia,Segmental Dystonia,Cervical Dystonia,Oculogyric Crisis,Oromandibular Dystonia,Spasmodic Dystonia,Hemidystonia,Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal,Cutis Laxa, Autosomal Dominant 3,Dystonia 3, Torsion, X-Linked,Leber Optic Atrophy And Dystonia,Early-Onset Parkinson'S Disease,Phenylketonuria,Hyperphenylalaninemia, Bh4-Deficient, A