Syndrome featuring ataxia. Medical search. Frequent questions

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Anatomy8

Cerebellum Purkinje Cells Brain Intranuclear Inclusion Bodies Cell Line Fibroblasts Cells, Cultured Chromosomes, Human, Pair 22

Organisms7

Porcine respiratory and reproductive syndrome virus Mice, Neurologic Mutants White spot syndrome virus 1 Mice, Knockout SARS Virus Mice, Transgenic Mice, Inbred C57BL

Diseases169

Ataxia Cerebellar Ataxia Syndrome Friedreich Ataxia Spinocerebellar Ataxias Gait Ataxia Ataxia Telangiectasia Down Syndrome Metabolic Syndrome X Nephrotic Syndrome Sjogren's Syndrome Turner Syndrome Abnormalities, Multiple Machado-Joseph Disease Myelodysplastic Syndromes Cushing Syndrome Acute Coronary Syndrome Polycystic Ovary Syndrome Williams Syndrome DiGeorge Syndrome Horner Syndrome Prader-Willi Syndrome Long QT Syndrome Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Compartment Syndromes Tourette Syndrome Antiphospholipid Syndrome Porcine Reproductive and Respiratory Syndrome Intellectual Disability Klinefelter Syndrome Angelman Syndrome Carpal Tunnel Syndrome Werner Syndrome Reye Syndrome Bartter Syndrome HELLP Syndrome Bloom Syndrome Brugada Syndrome Cerebellar Diseases Ehlers-Danlos Syndrome Respiratory Distress Syndrome, Adult Paraneoplastic Syndromes Ocular Motility Disorders Severe Acute Respiratory Syndrome Restless Legs Syndrome Job Syndrome Wiskott-Aldrich Syndrome Dysarthria Stiff-Person Syndrome Sweet Syndrome Miller Fisher Syndrome Apraxias Acquired Immunodeficiency Syndrome Churg-Strauss Syndrome Sturge-Weber Syndrome Disease Models, Animal Budd-Chiari Syndrome Chediak-Higashi Syndrome Wolff-Parkinson-White Syndrome Facies Kallmann Syndrome Sick Sinus Syndrome Stevens-Johnson Syndrome Fragile X Syndrome Sezary Syndrome Felty Syndrome Usher Syndromes Beckwith-Wiedemann Syndrome Immunologic Deficiency Syndromes Alagille Syndrome Nystagmus, Pathologic Myoclonic Cerebellar Dyssynergia Bardet-Biedl Syndrome ACTH Syndrome, Ectopic Peutz-Jeghers Syndrome Hemorrhagic Fever with Renal Syndrome Oculocerebrorenal Syndrome Cockayne Syndrome Smith-Lemli-Opitz Syndrome Nervous System Diseases Craniofacial Abnormalities Short Bowel Syndrome Behcet Syndrome Korsakoff Syndrome Zollinger-Ellison Syndrome Serotonin Syndrome Hepatopulmonary Syndrome Microcephaly Orofaciodigital Syndromes Proteus Syndrome Eye Abnormalities Duane Retraction Syndrome Ophthalmoplegia Complex Regional Pain Syndromes Olivopontocerebellar Atrophies Goldenhar Syndrome Epilepsies, Myoclonic Myoclonus Respiratory Distress Syndrome, Newborn Neuroleptic Malignant Syndrome Costello Syndrome Klippel-Feil Syndrome Subclavian Steal Syndrome Hantavirus Pulmonary Syndrome Opsoclonus-Myoclonus Syndrome Neoplastic Syndromes, Hereditary Thoracic Outlet Syndrome Hermanski-Pudlak Syndrome Chromosome Disorders Hearing Loss, Sensorineural LEOPARD Syndrome Reflex, Abnormal Heredodegenerative Disorders, Nervous System Muscle Hypotonia Hand Deformities, Congenital Li-Fraumeni Syndrome Hamartoma Syndrome, Multiple Mobius Syndrome Kearns-Sayre Syndrome Atrophy Hepatorenal Syndrome Waardenburg Syndrome Systemic Inflammatory Response Syndrome Sleep Apnea Syndromes Adie Syndrome Polyradiculoneuropathy Multiple System Atrophy Ovarian Hyperstimulation Syndrome Premenstrual Syndrome Capillary Leak Syndrome Neurocutaneous Syndromes Dwarfism Gitelman Syndrome Wolfram Syndrome Genetic Predisposition to Disease Acquired Hyperostosis Syndrome Acute Disease Chromosome Aberrations CREST Syndrome Wasting Syndrome Superior Vena Cava Syndrome Isaacs Syndrome Optic Atrophy Brain Diseases Chromosome Deletion Myasthenic Syndromes, Congenital Poland Syndrome Neurodegenerative Diseases Alstrom Syndrome Rubinstein-Taybi Syndrome Deafness Sudden Infant Death Nijmegen Breakage Syndrome Hypoplastic Left Heart Syndrome Romano-Ward Syndrome Syndactyly Rothmund-Thomson Syndrome Peripheral Nervous System Diseases Vitamin E Deficiency Growth Disorders Burning Mouth Syndrome Disease Progression Insulin Resistance Hypertelorism Lambert-Eaton Myasthenic Syndrome Zellweger Syndrome Tumor Lysis Syndrome Malignant Carcinoid Syndrome

Chemicals and Drugs15

Ataxia Telangiectasia Mutated Proteins Iron-Binding Proteins Tumor Suppressor Proteins Cell Cycle Proteins Protein-Serine-Threonine Kinases Nerve Tissue Proteins DNA-Binding Proteins Nuclear Proteins Fragile X Mental Retardation Protein Wiskott-Aldrich Syndrome Protein Kv1.1 Potassium Channel Biological Markers Autoantibodies Gliadin DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

Pedigree Magnetic Resonance Imaging DNA Mutational Analysis Disease Models, Animal Fatal Outcome Treatment Outcome Facies Risk Factors Case-Control Studies Retrospective Studies Severity of Illness Index Genetic Testing Chromosome Mapping Neurologic Examination Follow-Up Studies Prevalence Prospective Studies Reflex, Abnormal Tomography, X-Ray Computed Karyotyping Polymerase Chain Reaction Electrocardiography Cohort Studies Heterozygote Detection

Psychiatry and Psychology7

Tourette Syndrome Intellectual Disability Restless Legs Syndrome Apraxias Korsakoff Syndrome Asperger Syndrome Munchausen Syndrome

Phenomena and Processes31

Trinucleotide Repeat Expansion Mutation Trinucleotide Repeats Phenotype Genes, Recessive Mutation, Missense Consanguinity Genes, Dominant Heterozygote Homozygote DNA Damage Genetic Linkage Time Factors Base Sequence Genotype Alleles DNA Repeat Expansion Pregnancy Amino Acid Sequence Reflex, Abnormal DNA Repair Haplotypes Genetic Predisposition to Disease Point Mutation Chromosome Aberrations Exons Chromosomes, Human, Pair 22 Chromosome Deletion Mosaicism Gene Deletion Insulin Resistance

Information Science5

Molecular Sequence Data Fatal Outcome Base Sequence Prevalence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care13

Age of Onset Fatal Outcome Treatment Outcome Risk Factors Case-Control Studies Retrospective Studies Severity of Illness Index Genetic Testing Follow-Up Studies Prevalence Family Health Prospective Studies Cohort Studies

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care

Ataxia Cerebellar Ataxia Syndrome Friedreich Ataxia Spinocerebellar Ataxias Gait Ataxia Ataxia Telangiectasia Ataxia Telangiectasia Mutated Proteins Down Syndrome Metabolic Syndrome X Nephrotic Syndrome Iron-Binding Proteins Sjogren's Syndrome Turner Syndrome Abnormalities, Multiple Machado-Joseph Disease Pedigree Myelodysplastic Syndromes Trinucleotide Repeat Expansion Cushing Syndrome Mutation Acute Coronary Syndrome Polycystic Ovary Syndrome Williams Syndrome Trinucleotide Repeats DiGeorge Syndrome Cerebellum Horner Syndrome Prader-Willi Syndrome Long QT Syndrome Guillain-Barre Syndrome Phenotype Hemolytic-Uremic Syndrome Compartment Syndromes Tourette Syndrome Antiphospholipid Syndrome Porcine Reproductive and Respiratory Syndrome Intellectual Disability Klinefelter Syndrome Angelman Syndrome Carpal Tunnel Syndrome Tumor Suppressor Proteins Werner Syndrome Reye Syndrome Bartter Syndrome Porcine respiratory and reproductive syndrome virus Cell Cycle Proteins Genes, Recessive HELLP Syndrome Bloom Syndrome Magnetic Resonance Imaging Brugada Syndrome Cerebellar Diseases Ehlers-Danlos Syndrome Respiratory Distress Syndrome, Adult Protein-Serine-Threonine Kinases Mutation, Missense Age of Onset Paraneoplastic Syndromes Ocular Motility Disorders Severe Acute Respiratory Syndrome Purkinje Cells Restless Legs Syndrome Nerve Tissue Proteins Job Syndrome Wiskott-Aldrich Syndrome Dysarthria Stiff-Person Syndrome DNA-Binding Proteins Sweet Syndrome DNA Mutational Analysis Miller Fisher Syndrome Apraxias Acquired Immunodeficiency Syndrome Churg-Strauss Syndrome Sturge-Weber Syndrome Molecular Sequence Data Disease Models, Animal Consanguinity Budd-Chiari Syndrome Brain Fatal Outcome Chediak-Higashi Syndrome Genes, Dominant Nuclear Proteins Treatment Outcome Heterozygote Wolff-Parkinson-White Syndrome Facies Risk Factors Kallmann Syndrome Homozygote Sick Sinus Syndrome Stevens-Johnson Syndrome Fragile X Syndrome Sezary Syndrome Felty Syndrome DNA Damage Usher Syndromes Beckwith-Wiedemann Syndrome

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