Parkinson Disease 22, Autosomal Dominant; Park22

Clinical Features

Phenotypes and symptoms related to Parkinson Disease 22, Autosomal Dominant; Park22

  • Hyperreflexia
  • Tremor
  • Gait disturbance
  • Depressivity
  • Rigidity
  • Bradykinesia
  • Resting tremor
  • Kinetic tremor

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 22, Autosomal Dominant; Park22 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Parkinson Disease Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SLC6A3, SNCA, SPR, SYNJ1, TAF1, GIGYF2, UCHL1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, PARK7, RAB39B, LRRK2, CHCHD2, VPS13C, ATP13A2, EIF4G1, GBA , (...)

View the complete list with 4 more genes
Specificity
5 %
Genes
100 %
Parkinson Disease and Parkinsonism Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SLC20A2, SLC6A3, SNCA, SNCB, SPG11, SPR, SYNJ1, TAF1, TARDBP, TWNK, TH, GIGYF2, UCHL1, XPR1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, CHCHD10 , (...)

View the complete list with 48 more genes
Specificity
2 %
Genes
100 %
Parkinson Syndrome, autosomal dominant Panel.

By CeGaT GmbH (Germany).

SNCA, VPS35, HTRA2, LRRK2, CHCHD2, DNAJC13, EIF4G1, GBA, PRKAR1B, RAB29
Specificity
10 %
Genes
100 %
Parkinson all Panel.

By CeGaT GmbH (Germany).

ATXN2, SLC6A3, SNCA, SPG11, SPR, SYNJ1, TAF1, TH, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, PANK2, PARK7, RAB39B, ATP6AP2, LRRK2, ZFYVE26, CHCHD2 , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
100 %
CHCHD2.

By Fulgent Genetics Fulgent Genetics (United States).

CHCHD2
Specificity
100 %
Genes
100 %

You can get up to -3 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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