Definition of Familial Parkinson disease type 2Familial Parkinson disease type 2: A familial form of Parkinson disease inherited in an autosomal recessive manner due to mutation in the gene encoding parkin on chromosome 6q25.2-q27. Also known as PARK2. Source: MedTerms™ Medical Dictionaryhttp://www.medterms.com/script/main/art.asp?articlekey=25834 Last Editorial Review: 6/14/2012
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