Familial Parkinson disease type 11
Familial Parkinson disease type 11: A familial form of Parkinson disease inherited in an autosomal dominant manner due to a gene on chromosome 2q. Also known as PARK11.
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- Familial Parkinson disease type 2
Familial 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.
- Familial Parkinson disease type 3
Familial Parkinson disease type 3: A familial form of Parkinson disease inherited in an autosomal dominant manner due to a gene on chromosome 2p13. Also known as PARK3.
- Familial Parkinson disease type 4
Familial Parkinson disease type 4: A familial form of Parkinson disease inherited in an autosomal dominant manner due to a gene on chromosome 4p15. Also known as PARK4.
- Familial Parkinson disease type 5
Familial Parkinson disease type 5: A familial form of Parkinson disease inherited in an autosomal dominant manner due to mutation in the UCHL1 gene on chromosome 4p14. Also known as PARK5.
- Familial Parkinson disease type 6
Familial Parkinson disease type 6: A familial form of Parkinson disease inherited in an autosomal recessive manner due to mutation in a gene on chromosome 1p distinct from DJ1. Also known as PARK6.