Pigmented Nodular Adrenocortical Disease, Primary, 2; Ppnad2

Clinical Features

Top most frequent phenotypes and symptoms related to Pigmented Nodular Adrenocortical Disease, Primary, 2; Ppnad2

  • Hypertension
  • Kyphosis
  • Depressivity
  • Osteoporosis
  • Osteopenia
  • Anxiety
  • Mental deterioration
  • Bruising susceptibility
  • Round face
  • Psychosis

And another 11 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

Not enough data available about incidence and published cases.
No data available about the known clinical features onset.

Alternative names

Pigmented Nodular Adrenocortical Disease, Primary, 2; Ppnad2 Is also known as cushing syndrome, adrenal, due to ppnad2, pigmented micronodular adrenocortical disease, primary, 2.

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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Pigmented Nodular Adrenocortical Disease, Primary, 2; Ppnad2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Primary pigmented nodular adrenocortical disease type 3 (sequence analysis of PDE8B gene).

By CGC Genetics (Portugal).

PDE8B
Specificity
100 %
Genes
50 %
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
50 %
Neurogenetic Disorders - panels.

By MGZ Medical Genetics Center (Germany).

BCS1L, RTN2, RYR1, SACS, SCN1A, SCN1B, SCN2A, SCN8A, SCO1, SCO2, AIMP1, SDHA, SDHB, SDHC, SDHD, SGCE, SLC16A2, SLC17A5, SLC19A2, SLC1A3 , (...)

View the complete list with 572 more genes
Specificity
1 %
Genes
50 %
Autosomal-dominant striatal degeneration.

By Centogene AG - the Rare Disease Company (Germany).

PDE8B
Specificity
100 %
Genes
50 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company (Germany).

BCS1L, ROR2, RPL10, BDNF, RPS6KA3, RTN2, RYR1, SACS, BIN1, SBF1, SCN10A, SCN1A, SCN1B, SCN2A, SCN3A, SCN4A, SCN5A, SCN8A, SCN9A, SCO1 , (...)

View the complete list with 1177 more genes
Specificity
1 %
Genes
50 %
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
50 %
Atypical Parkinson syndrome Panel.

By CeGaT GmbH (Germany).

ATXN2, SPG11, SYNJ1, TH, FBXO7, DNAJC6, RAB39B, ATP6AP2, ZFYVE26, SLC30A10, DCTN1, C9orf72, ATP13A2, FMR1, FTL, GCH1, GRN, MAPT, ATXN3, ATP1A3 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
50 %
Autism Spectrum Disorders.

By Asper Biogene Asper Biogene LLC (Estonia).

RPL10, SCN1A, SCN2A, BRAF, SLC6A4, SLC6A8, CDKL5, MED12, TSC1, TSC2, UBE3A, HDAC8, CNTNAP2, FOXP2, CACNA1C, NSD1, PCDH19, NLGN4X, SHANK3, ZEB2 , (...)

View the complete list with 32 more genes
Specificity
2 %
Genes
50 %

We have 13 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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