Friedreich ataxia (FRDA) is an inherited neurodegenerative disorder classically characterized by progressive gait and limb ataxia, dysarthria, dysphagia, oculomotor dysfunction, loss of deep tendon reflexes, pyramidal tract signs, scoliosis, and in some, cardiomyopathy, diabetes mellitus, visual loss and defective hearing.

Synonyms: FRDA FA

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Term information

database cross reference
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OMIM:601992

MedDRA:10017374

UMLS:C0016719

ICD-10:G11.1

OMIM:229300

MeSH:D005621

notation

ORPHA:95

Term relations

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