Informaţii despre

Nume Ataxia-Oculomotor Apraxia 3
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Ataxia-Oculomotor Apraxia 4

Vezi şi

Boli A-Z Aceruloplasminemia Acute Disseminated Encephalomyelitis Acute Motor and Sensory Axonal Neuropathy Acute Motor Axonal Neuropathy Adenocarcinoma Adermatoglyphia Adrenoleukodystrophy Aging Albinism Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Al-Raqad Syndrome Aminoaciduria Aneurysm Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Apraxia 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-Pancytopenia Syndrome Ataxia-Telangiectasia Autoimmune Disease Autoimmune Encephalitis Autoimmune Polyendocrine Syndrome Autonomic Dysfunction Autosomal Dominant Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Disease Autosomal Recessive Sideroblastic Anemia Axonal Neuropathy Babesiosis Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Boucher-Neuhauser Syndrome Brain Injury Branchiootic Syndrome 1 Breast Cancer Camurati-Engelmann Disease Cataract Celiac Disease 1 Central Pontine Myelinolysis Cerebellar Ataxia and Neurosensory Deafness Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome Cerebellar Degeneration Cerebellar Disease Cerebritis Cerebrotendinous Xanthomatosis Cervical Dystonia Cervicitis Chickenpox Chikungunya Cholangiocarcinoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroiditis Chronic Active Epstein-Barr Virus Infection Ciliary Dyskinesia, Primary, 1 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Conjunctivitis Cortical Blindness Cranial Nerve Palsy Creutzfeldt-Jakob Disease Cystinuria Dementia Dentatorubral-Pallidoluysian Atrophy Diabetes Insipidus Diabetes Mellitus Diffuse Alveolar Hemorrhage Dystonia Ectodermal Dysplasia Encephalitis Encephalomyopathy Encephalopathy Endotheliitis Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica Epilepsy Erdheim-Chester Disease Essential Tremor Extrapontine Myelinolysis Familial Hemiplegic Migraine Fatal Familial Insomnia Focal Dystonia Ganglioneuroma Gerstmann-Straussler Disease Gillespie Syndrome Gordon Holmes Syndrome Graves' Disease Hemiplegic Migraine Hemophagocytic Lymphohistiocytosis Hepatocellular Carcinoma Hereditary Spastic Paraplegia Herpes Zoster Herpes Zoster Ophthalmicus Histiocytosis Hydrocephalus Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypotonia Insulin-Like Growth Factor I Internuclear Ophthalmoplegia Intracranial Aneurysm Ischemia Isoniazid Toxicity Krabbe Disease L-2-Hydroxyglutaric Aciduria Lambert-Eaton Myasthenic Syndrome Langerhans Cell Histiocytosis Laryngeal Abductor Paralysis Laryngitis Legionellosis Leptospirosis Leukemia Leukodystrophy Limbic Encephalitis Lupus Erythematosus Lyme Disease Machado-Joseph Disease Majeed Syndrome Malaria Marden-Walker Syndrome Marinesco-Sjogren Syndrome Meningitis Meningococcal Meningitis Meningoencephalitis Metachromatic Leukodystrophy Mevalonic Aciduria Microcephaly, Epilepsy, and Diabetes Syndrome Miller Fisher Syndrome Mitochondrial Complex Iii Deficiency Motor Neuron Disease Mucopolysaccharidosis, Type Vii Multiple Sclerosis Multiple System Atrophy 1 Mumps Myoclonus Myoclonus Epilepsy Myofibrillar Myopathy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Narcolepsy Nephronophthisis Neural Crest Tumor Neuritis Neuroblastoma Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy Neurosyphilis Obstructive Hydrocephalus Olivopontocerebellar Atrophy Opsoclonus-Myoclonus Syndrome Optic Neuritis Pancytopenia Papilloma Papillomatosis, Confluent and Reticulated Paraneoplastic Cerebellar Degeneration Paraneoplastic Syndromes Paraplegia Pellagra Plasmodium Falciparum Malaria Plasmodium Vivax Malaria Polydactyly Polyneuropathy Premature Ovarian Failure 1 Primary Cerebellar Degeneration Prion Disease Ptosis Refsum Disease, Classic Retinal Degeneration Retinitis Rosai-Dorfman Disease Sandhoff Disease Schizophrenia Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Siderosis Sjogren Syndrome Sleep Disorder Small Cell Carcinoma Smith-Kingsmore Syndrome Spastic Ataxia Spastic Diplegia Spasticity Spastic Paraparesis Spastic Paraplegia 20, Autosomal Recessive Spastic Paraplegia 46, Autosomal Recessive Spastic Paraplegia 7, Autosomal Recessive Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 13 Spinocerebellar Ataxia 19 Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 4 Spinocerebellar Ataxia, Autosomal Recessive 8 Spinocerebellar Degeneration Sporadic Adult-Onset Ataxia of Unknown Etiology Squamous Cell Carcinoma Stiff-Person Syndrome Strabismus Subcortical Arteriosclerotic Encephalopathy Superficial Siderosis Syne1-Related Autosomal Recessive Cerebellar Ataxia Systemic Lupus Erythematosus Teratoma Testicular Regression Syndrome Tetraamelia Syndrome, Autosomal Recessive Thrombocytopenia Thrombosis Thyroiditis Toxocariasis Traumatic Brain Injury Tremor Typhoid Fever Virus Associated Hemophagocytic Syndrome Vitamin B12 Deficiency West Nile Virus Whipple Disease Xanthomatosis Xeroderma Pigmentosum, Complementation Group F