Vezi şi

Boli A-Z Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Axonal Neuropathy Bainbridge-Ropers Syndrome Blood Group--Ahonen Cerebral Palsy Cerebritis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Dyskinetic Cerebral Palsy Dystonia Encephalopathy Epilepsy Exosc3-Related Pontocerebellar Hypoplasia Hepatic Adenomas, Familial Hereditary Ataxia Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypotonia Lissencephaly Malignant Hyperthermia Microcephaly Motor Neuron Disease Muscular Atrophy Muscular Dystrophy Myoclonus Neuronitis Neuropathy Paroxysmal Cold Hemoglobinuria Pontocerebellar Hypoplasia Type 1 Pontocerebellar Hypoplasia, Type 10 Pontocerebellar Hypoplasia, Type 1a Pontocerebellar Hypoplasia, Type 1b Pontocerebellar Hypoplasia, Type 2a Pontocerebellar Hypoplasia, Type 2d Pontocerebellar Hypoplasia, Type 2e Pontocerebellar Hypoplasia, Type 3 Pontocerebellar Hypoplasia, Type 4 Pontocerebellar Hypoplasia, Type 5 Pontocerebellar Hypoplasia, Type 6 Pontocerebellar Hypoplasia, Type 9 Pontoneocerebellar Hypoplasia Spinal Muscular Atrophy Tetraamelia Syndrome, Autosomal Recessive Tetralogy of Fallot Tsen54-Related Pontocerebellar Hypoplasia