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.
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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.
- Familial Parkinson disease type 7
Familial Parkinson disease type 7: A familial form of Parkinson disease inherited in an autosomal recessive manner due to mutation in the DJ1 gene on 1p36. Also known as PARK7.
- Familial Parkinson disease type 8
Familial Parkinson disease type 8: A familial form of Parkinson disease inherited in an autosomal dominant manner due to a gene on chromosome 12p11.2-q13.1. Also known as PARK8.
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Familial polyposis: An inherited condition in which several hundred polyps develop in the colon and rectum.
- Familial Parkinson disease type 9
Familial Parkinson disease type 9: A familial form of Parkinson disease inherited in an autosomal recessive manner due to a gene on chromosome 1p36. Also known as PARK9.