Parkinson Disease 4, Autosomal Dominant; Park4
Clinical Features
Top most frequent phenotypes and symptoms related to Parkinson Disease 4, Autosomal Dominant; Park4
- Generalized hypotonia
- Cognitive impairment
- Tremor
- Dementia
- Weight loss
- Rigidity
- Parkinsonism
- Gliosis
- Hypotension
- Memory impairment
And another 12 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.
Alternative names
Parkinson Disease 4, Autosomal Dominant; Park4 Is also known as parkinson disease 4, autosomal dominant lewy body.
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 4, Autosomal Dominant; Park4 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Alpha Synuclein (SNCA) Duplication/Deletion Test.
By Athena Diagnostics Inc (United States).
SNCA
Specificity
100 %
Genes
100 % |
|
Alpha Synuclein (SNCA) DNA Sequencing Test.
By Athena Diagnostics Inc (United States).
SNCA
Specificity
100 %
Genes
100 % |
|
Complete Parkinsonism Evaluation.
By Athena Diagnostics Inc (United States).
SNCA, PINK1, PARK7, LRRK2, PRKN
Specificity
20 %
Genes
100 % |
|
Movement Disorders Panel.
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 % |
|
Parkinson's Disease.
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 % |
 SNCA.
By Institute for Human Genetics University Clinic Freiburg (Germany).
SNCA
Specificity
100 %
Genes
100 % |
 SNCA. Complete sequencing.
By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
SNCA
Specificity
100 %
Genes
100 % |
|
SNCA. MLPA testing.
By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
SNCA
Specificity
100 %
Genes
100 % |
You can get up to 48 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE; EBSDM HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD OPSISMODYSPLASIA; OPSMD LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6 ROBINOW-SORAUF SYNDROME