Disease Information for Friedreich's Ataxia: Disease Mechanism & Classification

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Class
CLASS/Pediatric disorders (ex)
CLASS/Cerebellar disorder (ex)
CLASS/Neurologic (category)
CLASS/Spinal cord disorder (ex)
Pathophysiology
Pathophysiology/Frataxin gene mutation
Pathophysiology/GAA intron repeats then severe
Pathophysiology/Gene locus 9q13
Pathophysiology/Gene locus Chromosome 9
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic base pair repeats mutation
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Demyelination
Pathophysiology/Neurologic degenerative disorder (ex)
Pathophysiology/Posterior columns cord def
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Eponymic (category)
PROCESS/Genetic expressivity variable (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Movement disorder (ex)
PROCESS/Congenital CNS disorder (ex)
PROCESS/Developmental degenerative neurological disorder (ex)
PROCESS/Hereditary ataxia disorder (ex)
PROCESS/Hereditary SCA (spinocerebellar ataxias)
PROCESS/Hereditory motor/sensory neuropathy (ex)
PROCESS/Myelin involvement/disorder (ex)
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