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.

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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 more

Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

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