Alzheimer Disease 9, Susceptibility To; Ad9

Clinical Features

Top most frequent phenotypes and symptoms related to Alzheimer Disease 9, Susceptibility To; Ad9

  • Behavioral abnormality
  • Depressivity
  • Cerebral cortical atrophy
  • Parkinsonism
  • Memory impairment
  • Neuronal loss in central nervous system
  • Abnormality of extrapyramidal motor function
  • Alzheimer disease
  • Neurofibrillary tangles
  • Delusions

And another 3 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

Alzheimer Disease 9, Susceptibility To; Ad9 Is also known as alzheimer disease 9, late-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.


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Alzheimer Disease 9, Susceptibility To; Ad9 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Autism Spectrum Disorders Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SCN1A, SCN2A, SGSH, BRAF, SLC6A1, SLC9A6, SPAST, CDKL5, STXBP1, SYN2, TBR1, TCF20, TCF4, TSC1, TSC2, UBE3A, BCL11A, CNTNAP2, CACNA1C, CSMD1 , (...)

View the complete list with 85 more genes
Specificity
1 %
Genes
100 %
Alzheimer's disease Panel.

By CeGaT GmbH (Germany).

TBP, VPS35, MARK4, NLGN1, CD33, TOMM40, ABCA7, APOE, APP, PSEN1, PSEN2
Specificity
10 %
Genes
100 %
Dementia all Panel.

By CeGaT GmbH (Germany).

ATXN2, SQSTM1, TARDBP, TBK1, TBP, TUBA4A, UBQLN2, VCP, VPS35, MARK4, NLGN1, CHCHD10, CD33, OPTN, TREM2, TOMM40, CSF1R, CHMP2B, DCTN1, C9orf72 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
100 %
ABCA7.

By Fulgent Genetics Fulgent Genetics (United States).

ABCA7
Specificity
100 %
Genes
100 %
Dementia Panel.

By Blueprint Genetics (Finland).

SNCA, SORL1, TARDBP, TUBA4A, UBE3A, UBQLN2, VCP, TREM2, RNF216, CSF1R, CHMP2B, ABCA7, FUS, GRN, APOE, APP, MAPT, SIGMAR1, PRNP, PSEN1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %

We have -3 more panels available in our App

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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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