Heredodegenerative Disorders, Nervous System

Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System

Adrenal Hyperplasia, Congenital | Alagille Syndrome | Anemia, Hemolytic, Congenital | Anemia, Hypoplastic, Congenital | Angioedema, Hereditary | Ataxia Telangiectasia | Blood Coagulation Disorders, Inherited | Brugada Syndrome | CADASIL | Camurati-Engelmann Syndrome | Cardiomyopathy, Hypertrophic, Familial | Cherubism | Chromosome Disorders | Cystic Fibrosis | Dwarfism | Eye Diseases, Hereditary | Familial Mediterranean Fever | Genetic Diseases, X-Linked | Genetic Diseases, Y-Linked | Hajdu-Cheney Syndrome | Hemoglobinopathies | Hyperthyroxinemia, Familial Dysalbuminemic | Kallmann Syndrome | Kartagener Syndrome | Lewy Body Disease | Marfan Syndrome | Metabolism, Inborn Errors | Motor Neuron Disease | Multiple System Atrophy | Muscular Dystrophies | Myasthenic Syndromes, Congenital | Nail-Patella Syndrome | Neoplastic Syndromes, Hereditary | Olivopontocerebellar Atrophies | Osteogenesis Imperfecta | Pain Insensitivity, Congenital | Paraneoplastic Syndromes, Nervous System | Parkinson Disease | Postpoliomyelitis Syndrome | Prion Diseases | Shy-Drager Syndrome | Skin Diseases, Genetic | Subacute Combined Degeneration | Tauopathies | Werner Syndrome

Heredodegenerative Disorders, Nervous System > Alexander Disease | Amyloid Neuropathies, Familial | Canavan Disease | Cockayne Syndrome | Dystonia Musculorum Deformans | Gerstmann-Straussler-Scheinker Disease | Hepatolenticular Degeneration | Hereditary Central Nervous System Demyelinating Diseases | Hereditary Motor and Sensory Neuropathies | Hereditary Sensory and Autonomic Neuropathies | Huntington Disease | Lafora Disease | Lesch-Nyhan Syndrome | Menkes Kinky Hair Syndrome | Mental Retardation, X-Linked | Myotonia Congenita | Myotonic Dystrophy | Neuroacanthocytosis | Neurofibromatoses | Neuronal Ceroid-Lipofuscinoses | Optic Atrophies, Hereditary | Pantothenate Kinase-Associated Neurodegeneration | Rett Syndrome | Spinal Muscular Atrophies of Childhood | Spinocerebellar Degenerations | Tourette Syndrome | Tuberous Sclerosis | Unverricht-Lundborg Syndrome