Parkinson Disease 22, Autosomal Dominant; Park22

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Parkinson Disease 22, Autosomal Dominant; Park22

CHCHD2

View recommended genes panels

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 Panel complete gene list SLC6A3, SNCA, SPR, SYNJ1, TAF1, GIGYF2, UCHL1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, PARK7, RAB39B, LRRK2, CHCHD2, VPS13C, ATP13A2, EIF4G1, GBA, GCH1, MAPT, PRKN, PLA2G6 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 Panel complete gene list SLC20A2, SLC6A3, SNCA, SNCB, SPG11, SPR, SYNJ1, TAF1, TARDBP, TWNK, TH, GIGYF2, UCHL1, XPR1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, CHCHD10, PARK7, RAB39B, ATP6AP2, LRRK2, LYST, CLN3, SLC39A14, CHCHD2, CP, VPS13C, CSF1R, SLC30A10, C19orf12, DCAF17, ADORA1, DCTN1, DNAJC12, WDR45, DNM1L, TENM4, ATP13A2, DNAJC13, EIF4G1, PTRHD1, FTL, GBA, GCH1, GRN, DNAJB2, APP, KIF5A, MAPT, ATP1A3, PRKN, PDE10A, PDE8B, PDGFB, PDGFRB, PLA2G6, PODXL, POLG, POLG2, PRKAR1B, PRKRA, PRNP, PSEN1, PSEN2, RAB29 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 Panel complete gene list ATXN2, SLC6A3, SNCA, SPG11, SPR, SYNJ1, TAF1, TH, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, PANK2, PARK7, RAB39B, ATP6AP2, LRRK2, ZFYVE26, CHCHD2, VPS13C, SLC30A10, C19orf12, DCTN1, TENM4, ATP13A2, DNAJC13, EIF4G1, FMR1, FTL, GBA, GCH1, GRN, MAPT, ATXN3, ASNA1, ATP1A3, PRKN, PDE10A, PDE8B, PLA2G6, PODXL, POLG, PRKAR1B, PRKRA, PTEN, RAB29 Specificity 3 % Genes 100 %
CHCHD2. By Fulgent Genetics Fulgent Genetics (United States). CHCHD2 Specificity 100 % Genes 100 %

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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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