Pigmented nodular adrenocortical disease, primary, 3

Synonyms: CUSHING SYNDROME, ADRENAL, DUE TO PPNAD3

Summary

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE8B gene. [from MONDO]

Available tests

10 tests are in the database for this condition.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

PDE8B
29 tests
Also known as: ADSD, PPNAD3, PDE8B
Summary: phosphodiesterase 8B

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the endocrine system
- Adrenal hyperplasia
  Adrenal hyperplasia
  - MedGen UID: 301220
  - Concept ID: C1621895
  - Finding: Disease or Syndrome
  Abnormality of the endocrine system
  See: Feature record | Search on this feature
- Increased circulating cortisol level
  Increased circulating cortisol level
  - MedGen UID: 871175
  - Concept ID: C4025651
  - Finding: Finding
  Abnormality of the endocrine system
  See: Feature record | Search on this feature

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Clinical resources

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