Parkinson Disease 8, Autosomal Dominant; Park8
Clinical Features
Top most frequent phenotypes and symptoms related to Parkinson Disease 8, Autosomal Dominant; Park8
- Seizures
- Cognitive impairment
- Delayed speech and language development
- Tremor
- Dementia
- Cerebral cortical atrophy
- Rigidity
- Mental deterioration
- Postural instability
- Parkinsonism
And another 21 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Parkinson Disease 8, Autosomal Dominant; Park8 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Athena Diagnostics Inc (United States).
LRRK2
Specificity
100 %
Genes
100 % |
![]() By Athena Diagnostics Inc (United States).
SNCA, PINK1, PARK7, LRRK2, PRKN
Specificity
20 %
Genes
100 % |
![]() By Athena Diagnostics Inc (United States).
LRRK2
Specificity
100 %
Genes
100 % |
![]() By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
SCP2, SGCE, SLC20A2, SLC2A1, SLC6A3, SNCA, SPR, SQSTM1, SUCLA2, SUOX, TAF1, TH, TIMM8A, TREX1, MCOLN1, VPS35, FBXO7, CACNA1A, NPC2, PINK1 , (...)
View the complete list with 72 more genes
Specificity
2 %
Genes
100 % |
![]() By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
SLC6A3, SNCA, TAF1, TH, VPS35, FBXO7, PINK1, PARK7, LRRK2, CSF1R, DCTN1, ATP13A2, GBA, GCH1, MAPT, ATP1A3, PRKN, PLA2G6, POLG
Specificity
6 %
Genes
100 % |
![]() By Institute for Human Genetics University Clinic Freiburg (Germany).
LRRK2
Specificity
100 %
Genes
100 % |
![]() By Neurogenetics Department Cyprus Institute of Neurology and Genetics (Cyprus).
LRRK2
Specificity
100 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
LRRK2
Specificity
100 %
Genes
100 % |
You can get up to 45 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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