Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia; Als10

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 Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia; Als10

TARDBP

Clinical Features

Top most frequent phenotypes and symptoms related to Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia; Als10

Ataxia
Spasticity
Cognitive impairment
Dysarthria
Skeletal muscle atrophy
Gait disturbance
Dysphagia
Respiratory insufficiency
Edema
Congestive heart failure

And another 26 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.

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.

Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia; Als10 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Amyotrophic Lateral Sclerosis Advanced Evaluation. By Athena Diagnostics Inc (United States). SOD1, SQSTM1, TARDBP, UBQLN2, VAPB, VCP, FIG4, OPTN, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, SIGMAR1, PFN1 Specificity 6 % Genes 100 %
Nonprevalent Amyotrophic Lateral Sclerosis Advanced Sequencing Evaluation. By Athena Diagnostics Inc (United States). SQSTM1, TARDBP, UBQLN2, VAPB, VCP, FIG4, OPTN, CHMP2B, DCTN1, FUS, ALS2, SETX, ANG, SIGMAR1, PFN1 Specificity 7 % Genes 100 %
Amyotrophic Lateral Sclerosis. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). ATXN2, SOD1, TARDBP, UBQLN2, VAPB, VCP, VEGFA, FIG4, OPTN, SPART, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, NEFH, SIGMAR1, PFN1 , (...) View the complete list with 1 more genes Panel complete gene list ATXN2, SOD1, TARDBP, UBQLN2, VAPB, VCP, VEGFA, FIG4, OPTN, SPART, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, NEFH, SIGMAR1, PFN1, PRPH2 Specificity 5 % Genes 100 %
Dementia. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). SORL1, TARDBP, VCP, FIG4, OPTN, TREM2, CSF1R, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, GRN, ANG, APOE, APP, MAPT, PRNP, PSEN1 , (...) View the complete list with 1 more genes Panel complete gene list SORL1, TARDBP, VCP, FIG4, OPTN, TREM2, CSF1R, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, GRN, ANG, APOE, APP, MAPT, PRNP, PSEN1, PSEN2 Specificity 5 % Genes 100 %
Familial Amyotrophic Lateral Sclerosis 10. By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust (United Kingdom). TARDBP Specificity 100 % Genes 100 %
TAR DNA binding protein TARDBP (TDP-43) gene sequencing test. By Neurogenetics Department Cyprus Institute of Neurology and Genetics (Cyprus). TARDBP Specificity 100 % Genes 100 %
TDP43. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). TARDBP Specificity 100 % Genes 100 %
TARDBP. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). TARDBP Specificity 100 % Genes 100 %

You can get up to 63 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Search Engine

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