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Possible Causes For Ataxia Disorder - Causes: Hereditary, Familial, Genetic Disorders
List of current finding(s):
Ataxia Disorder - Causes
- Trauma Causes (6)
- Electromagnetic, Physics, trauma, Radiation Causes (5)
- Iatrogenic, Self Induced Disorders (1)
- Surgical, Procedure Complication (1)
- Infectious Disorders (Specific Agent) (35)
- Infected organ, Abscesses (8)
- Granulomatous, Inflammatory Disorders (1)
- Neoplastic Disorders (24)
- Allergic, Collagen, Auto-Immune Disorders (11)
- Metabolic, Storage Disorders (18)
- Biochemical Disorders (4)
- Deficiency Disorders (7)
- Congenital, Developmental Disorders (19)
- Hereditary, Familial, Genetic Disorders (35)
- Usage, Degenerative, Necrosis, Age Related Disorders (12)
- Relational, Mental, Psychiatric Disorders (4)
- Anatomic, Foreign Body, Structural Disorders (8)
- Arteriosclerotic, Vascular, Venous Disorders (18)
- Functional, Physiologic Variant Disorders (1)
- Vegetative, Autonomic, Endocrine Disorders (15)
- Reference to Organ System (19)
- Heirarchical Major Groups (3)
- Drugs (46)
- Poisoning (Specific Agent) (60)
- Organ Poisoning (Intoxication) (2)
- Definition
- External Links Related to Ataxia Disorder - Causes
- Hereditary, Familial, Genetic Disorders:
- Ataxia-telangiectasia
- Cerebellar hereditofamilial degen.
- Hereditary neuropathy
- Huntington's chorea
- Myoclonic encephalopathy/childhood
- Neuropathy, hypertrophic interstitial
- Neuropathy, sensory radicular, heredit.
- Paraplegia, spastic hereditary
- Ataxia/Oculomotor apraxia syndrome (9p13.3)
- Mitochondrial myopathy/MERRF
- Schilder disease/Adrenoleukodystrophy
- Dominant SCA/Spinal Cerebellar ataxias
- Cerebellar ataxia, congenital/hered.
- Encephalomyelopathy/necro/subact/Leigh
- Friedreich's Ataxia
- Hallervorden-Spatz disease (PKAN/NBIA)
- Hereditary/neurologic degeneration synd
- Kearns-Sayre Ophthalmoplegic Syndrome
- Leukodystrophy, Krabbe
- Olivopontocerebellar degeneration
- Parkinsonism, juvenile, of Hunt
- Pelizaeus-Merzbacher disease
- Refsum's disease
- Roussy-Levy syndrome
- Spinocerebellar ataxia, Hered/Type I
- Spinopontine Atrophy /MJD disease
- Von Hipple-Lindau disease/Retinocerebellar angiomas
- Cerebellar ataxia/Cayman type
- Episodic ataxia/EA-2/Hemiplegic migraine
- Giant axonal neuropathy, hereditary
- Hereditary dysmyelinating neuropathy
- Hereditary sensory neuropathy (type II)
- Neuhauser Syndrome
- Segawa Syndrome/Infant Parkinsonism
- Vitamin E deficiency/dependence familial ataxia
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