Vezi şi

Boli A-Z Abetalipoproteinemia Acute Respiratory Distress Syndrome Adrenoleukodystrophy Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Beta2m Amyotonia Congenita Amyotrophy, Monomelic Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Anterior Spinal Artery Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autonomic Dysfunction Axonal Neuropathy Beckwith-Wiedemann Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Wright Antigen Bone Fracture Cataract Central Core Myopathy Cerebellar Hypoplasia Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2d Charcot-Marie-Tooth Disease, Axonal, Type 2k Chiari Malformation Chromosomal Triplication Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Congenital Contractures Congenital Hypothyroidism Corneal Dystrophy, Thiel-Behnke Type Cortical Dysplasia, Complex, with Other Brain Malformations 7 Cystic Fibrosis Cystinuria Dandy-Walker Complex Diabetes Mellitus Distal Hereditary Motor Neuropathy Type 7 Distal Hereditary Motor Neuropathy, Type V Dysautonomia Dysphagia Encephalopathy Epilepsy Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Exudative Vitreoretinopathy Farber Lipogranulomatosis Fragile X Syndrome Galactose Epimerase Deficiency Hepatic Adenomas, Familial Hereditary Motor and Sensory Neuropathy, Type Iic Hereditary Spastic Paraplegia Hip Subluxation Hypertonia Hypoplastic Left Heart Syndrome Hypotonia Hypoxia Immune Suppression Intestinal Pseudo-Obstruction Joint Disorders Juvenile Spinal Muscular Atrophy Kagami-Ogata Syndrome Kaposiform Hemangioendothelioma Kaufman Oculocerebrofacial Syndrome Laryngitis Lateral Sclerosis Limb-Girdle Muscular Dystrophy Long Qt Syndrome 1 Mcleod Syndrome Microphthalmia, Isolated 1 Motor Neuron Disease Mucolipidosis Iv Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Muscle Hypertrophy Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne and Becker Type Myasthenia Gravis Myopathy Myotonia Myotonic Dystrophy Neonatal Adrenoleukodystrophy Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronitis Neuronopathy, Distal Hereditary Motor, Type Va Neuronopathy, Distal Hereditary Motor, Type Viia Neuropathy Olivopontocerebellar Atrophy Pancreatitis Paraplegia Pelizaeus-Merzbacher Disease Poland Syndrome Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia, Type 1a Pontocerebellar Hypoplasia, Type 1c Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures Progressive Muscular Atrophy Proximal Spinal Muscular Atrophy Retinitis Rett Syndrome Rhabdomyosarcoma Roussy-Levy Hereditary Areflexic Dystasia Scapuloperoneal Spinal Muscular Atrophy Scoliosis Spasticity Spinal Disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Iv Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy Spinal Muscular Atrophy, X-Linked 2 Status Epilepticus Survival Motor Neuron Spinal Muscular Atrophy Tetanus Tetraamelia Syndrome, Autosomal Recessive Thrombosis Tooth Disease Tremor Undifferentiated Pleomorphic Sarcoma Wallerian Degeneration