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GTR Home > Conditions/Phenotypes > Pigmented nodular adrenocortical disease, primary, 2

Pigmented nodular adrenocortical disease, primary, 2

Synonyms
CUSHING SYNDROME, ADRENAL, DUE TO PPNAD2; PIGMENTED MICRONODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2

Summary

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE11A gene. [from MONDO]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: PPNAD2, PDE11A
    Summary: phosphodiesterase 11A

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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