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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
- Eponymic
- Functional-Physiologic
- Hereditofamilial
- Iatrogenic
- Idiopathic
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- Infectious agent
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- Trauma
- Use-age-Atrophic
- Endocrine-Vegetative
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Information for Cerebellar hereditofamilial degen.
- Clinical Manifestations
- Signs & Symptoms
- Action Tremor
- Ataxia
- Ataxia, Cerebellar type
- Ataxia/Motor tremor type
- Cerebellar movement disorder/signs
- Cerebellar signs
- Dysdiadochokinesia/Alternating failure
- Gait disturbance/abnormality
- Involuntary Leg Movement Standing
- Limb Ataxia
- Movement or gait disorder/signs
- Nystagmus
- Poor coordination legs/feet
- Staggering Gait
- Titubation Cerebellar Stagger/Nodding tremor
- Tremor
- Tremor in Elderly
- Tremor,coarse
- Tremor,intention
- Unable to tandem walk/straight line
- Unsteadiness movement/Gait in a child
- Balance problems
- Falling
- Walking difficulties
- True Vertigo Sign Confirmed
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Ataxia
- Family history/Gait disorders
- Family history/Tremor
- Sex & Age Groups
- Population/Child
- Population/Children/all
- Diagnostic Test Results
- CT Scan
- CT Scan/Head Brain/cerebellar atrophy
- MRI/Head Cerebellar atrophy
- Associated Diseases & Rule outs
- Rule Outs
- Friedreich's Ataxia
- Associated Disease & Complications
- Cerebellar ataxia
- Ataxia Disorder
- Disease Mechanism & Classification
- Class
- CLASS/Brain/CNS disorder (ex)
- CLASS/Cerebellar disorder (ex)
- CLASS/Neurologic (category)
- Pathophysiology
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Hereditary disease/Adult manifestations
- Pathophysiology/CNS degeneration
- Pathophysiology/Neurologic degenerative disorder (ex)
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Hereditofamilial (category)
- PROCESS/Use/Age/atrophic disorder (category)
- PROCESS/Developmental degenerative neurological disorder (ex)
- PROCESS/Hereditary ataxia disorder (ex)
- PROCESS/Hereditary SCA (spinocerebellar ataxias)
- Definition
- Be the first to add a definition for Cerebellar hereditofamilial degen.
- External Links Related to Cerebellar hereditofamilial degen.
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)