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Nume Autosomal Dominant Cerebellar Ataxia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Autosomal Recessive Cerebellar Ataxia

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Boli A-Z 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Aceruloplasminemia Adie Pupil Aging Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Amyloidosis, Hereditary, Transthyretin-Related Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Apraxia Arbitrary Restriction Polymorphism 1 Argyll Robertson Pupil Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Aural Atresia, Congenital Autonomic Dysfunction Axonal Neuropathy Back Pain Blepharospasm Blood Group--Ahonen Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Brainstem Auditory Evoked Responses Brugada Syndrome Central Nervous System Origin Vertigo Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant Cerebellar Degeneration Cerebellar Disease Cerebello-Olivary Atrophy Cerebral Degeneration Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Ceroid Lipofuscinosis, Neuronal, 2 Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease, Axonal, Type 2t Childhood Apraxia of Speech Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroiditis Coarctation of Aorta Cognitive Function 1, Social Cone Dystrophy Creutzfeldt-Jakob Disease Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dementia Dentatorubral-Pallidoluysian Atrophy Dysautonomia Dysphagia Dystonia Encephalopathy Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endotheliitis Ependymoma Epilepsy Episodic Ataxia Episodic Ataxia, Type 1 Episodic Ataxia, Type 2 Episodic Ataxia, Type 6 Episodic Ataxia, Type 7 Essential Tremor Familial Hemiplegic Migraine Fanconi Anemia, Complementation Group E Focal Dystonia Focal Epilepsy Friedreich Ataxia 1 Hemiplegic Migraine Hepatic Adenomas, Familial Hepatitis Hereditary Ataxia Hereditary Spastic Paraplegia Huntington Disease Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Internuclear Ophthalmoplegia Kearns-Sayre Syndrome Laryngitis Lateral Sclerosis Leber Congenital Amaurosis 4 Leber Hereditary Optic Neuropathy Lupus Erythematosus Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Machado-Joseph Disease Majeed Syndrome Mannosidosis Mannosidosis, Beta a, Lysosomal Mitochondrial Dna Depletion Syndrome 7 Mood Disorder Motor Neuron Disease Multiple Sclerosis Multiple System Atrophy 1 Multiple System Atrophy, Cerebellar Type Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Myoclonus Myoclonus Epilepsy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myotonic Dystrophy Narcolepsy Neurodegeneration with Brain Iron Accumulation 2a Neuronal Ceroid Lipofuscinosis Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy Ocular Motor Apraxia Olivopontocerebellar Atrophy Paraplegia Parkinson Disease 7, Autosomal Recessive Early-Onset Parkinson Disease, Late-Onset Polyneuropathy Premature Ovarian Failure 1 Primary Cerebellar Degeneration Progressive Myoclonus Epilepsy Restless Legs Syndrome Retinal Degeneration Retinitis Schizophrenia Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Sideroblastic Anemia Siderosis Sleep Disorder Spastic Ataxia Spastic Ataxia 1, Autosomal Dominant Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Paraparesis Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 10 Spinocerebellar Ataxia 11 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 13 Spinocerebellar Ataxia 14 Spinocerebellar Ataxia 15 Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 18 Spinocerebellar Ataxia 19 Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 20 Spinocerebellar Ataxia 21 Spinocerebellar Ataxia 23 Spinocerebellar Ataxia 25 Spinocerebellar Ataxia 26 Spinocerebellar Ataxia 27 Spinocerebellar Ataxia 28 Spinocerebellar Ataxia 29 Spinocerebellar Ataxia 30 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 32 Spinocerebellar Ataxia 34 Spinocerebellar Ataxia 35 Spinocerebellar Ataxia 36 Spinocerebellar Ataxia 37 Spinocerebellar Ataxia 38 Spinocerebellar Ataxia 4 Spinocerebellar Ataxia 43 Spinocerebellar Ataxia 5 Spinocerebellar Ataxia 6 Spinocerebellar Ataxia 7 Spinocerebellar Ataxia 8 Spinocerebellar Ataxia 9 Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Ataxia, Autosomal Recessive 20 Spinocerebellar Ataxia, Autosomal Recessive 3 Spinocerebellar Ataxia, Autosomal Recessive 7 Spinocerebellar Ataxia Type 16 Spinocerebellar Ataxia Type 19/22 Spinocerebellar Ataxia Type 1 with Axonal Neuropathy Spinocerebellar Degeneration Stiff-Person Syndrome Superficial Siderosis Swallowing Disorders Systemic Lupus Erythematosus Temporal Lobe Epilepsy Tremor