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Boli A-Z Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Autosomal Dominant Cerebellar Ataxia Bladder Transitional Cell Papilloma Blood Group--Ahonen Blood Group, Dombrock System Blood Group--Rhesus System E Polypeptide Cerebellar Atrophy, Developmental Delay, and Seizures Cerebral Atrophy Cerebritis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chronic Progressive External Ophthalmoplegia Cowpox Dementia Dentatorubral-Pallidoluysian Atrophy Dystonia Familial Adenomatous Polyposis Familial Adenomatous Polyposis 1 Fanconi Anemia, Complementation Group E Fetal Alcohol Spectrum Disorder Friedreich Ataxia 1 Hepatic Adenomas, Familial Hereditary Ataxia Hereditary Spastic Paraplegia Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction Huntington Disease-Like 2 Hydrocephalus Juvenile Huntington Disease Leber Hereditary Optic Neuropathy Lipoid Proteinosis of Urbach and Wiethe Machado-Joseph Disease Miller-Dieker Lissencephaly Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Myotonic Dystrophy Neuronitis Neuropathy Ocular Dominance Paraplegia Porphyria Porphyria Variegata Prion Disease Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Retinal Ischemia Rett Syndrome Short-Rib Thoracic Dysplasia 4 with or Without Polydactyly Spasticity Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 17 Spinocerebellar Degeneration Status Epilepticus Substance Abuse Tardive Dyskinesia Tic Disorder Toxic Encephalopathy Tremor Trichotillomania Wilson Disease
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