Informaţii despre

Nume Hereditary Ataxia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Hereditary ataxia
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Aceruloplasminemia Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autosomal Dominant Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Axonal Neuropathy Basal Ganglia Disease Blood Group--Ahonen Cerebellar Degeneration Cerebellar Disease Cerebritis Chronic Progressive External Ophthalmoplegia Dentatorubral-Pallidoluysian Atrophy Dysphagia Encephalopathy Essential Tremor Friedreich Ataxia 1 Hepatic Adenomas, Familial Hereditary Spastic Paraplegia Hydrolethalus Syndrome 1 Leber Congenital Amaurosis 4 Machado-Joseph Disease Mitochondrial Disorders Multiple Sclerosis Muscular Atrophy Myoclonus Neuritis Neuronal Intranuclear Inclusion Disease Neuropathy Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Olivopontocerebellar Atrophy Paraplegia Parkinson Disease, Late-Onset Pontocerebellar Hypoplasia Primary Cerebellar Degeneration Retinal Degeneration Retinitis Seizures, Benign Familial Neonatal, 1 Spastic Ataxia Spasticity Spastic Paraparesis Spastic Paraplegia 7, Autosomal Recessive Speech Disorder Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 18 Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 28 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 36 Spinocerebellar Ataxia 6 Spinocerebellar Ataxia 7 Spinocerebellar Ataxia 8 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy Spinocerebellar Ataxia Type 1 with Axonal Neuropathy Spinocerebellar Degeneration Tremor