Informaţii despre

Nume Friedreich Ataxia 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Early-onset cerebellar ataxia
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Friedreich Ataxia 2

Vezi şi

Boli A-Z Aceruloplasminemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Anemia, Sideroblastic, 1 Anemia, Sideroblastic, and Spinocerebellar Ataxia Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia with Vitamin E Deficiency Atransferrinemia Atrial Standstill 1 Autosomal Dominant Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Axonal Neuropathy Blood Group--Ahonen Blood Group, I System Brainstem Auditory Evoked Responses Cerebellar Degeneration Cerebellar Disease Cerebritis Charcot-Marie-Tooth Disease Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Colonic Pseudo-Obstruction Combined Oxidative Phosphorylation Deficiency 19 Cone-Rod Dystrophy 2 Congestive Heart Failure Dentatorubral-Pallidoluysian Atrophy Diabetes Mellitus Dysphagia Dystonia Encephalopathy Epilepsy Fanconi Anemia, Complementation Group a Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Fragile X Syndrome Friedreich Ataxia 2 Fundus Albipunctatus Growth Hormone Deficiency Hemochromatosis, Type 1 Hepatitis Hereditary Ataxia Hypertrophic Cardiomyopathy Ichthyosis Prematurity Syndrome Infantile Cerebellar-Retinal Degeneration Inflammatory Bowel Disease Lactic Acidosis Laryngitis Machado-Joseph Disease Mitochondrial Disorders Mucolipidosis Iv Muscular Atrophy Myoclonus Myoclonus Epilepsy Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neuropathy Osteogenic Sarcoma Pancreatitis Primary Cerebellar Degeneration Progressive Myoclonus Epilepsy Restless Legs Syndrome Sarcoma Scoliosis Siderosis Sleep Disorder Spasmodic Dystonia Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Speech Disorder Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Muscular Atrophy Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 18 Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 6 Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Degeneration Tay-Sachs Disease Tetraamelia Syndrome, Autosomal Recessive Tooth Disease Tremor Tuberous Sclerosis Vitamin E, Familial Isolated Deficiency of