Pigmented Nodular Adrenocortical Disease, Primary, 2 (PPNAD2)

Alias:

Ppnad2

Adrenocortical Disease, Nodular, Pigmented, Primary, Type 2

Pigmented Micronodular Adrenocortical Disease, Primary, 2

Primary Pigmented Micronodular Adrenocortical Disease 2

Primary Pigmented Nodular Adrenocortical Disease 2

Primary Pigmented Nodular Adrenocortical Disease-2

Cushing Syndrome, Adrenal, Due to Ppnad2

Adrenal Cushing Syndrome Due to Ppnad2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Pigmented Nodular Adrenocortical Disease, Primary, 2, also known as ppnad2, is related to primary pigmented nodular adrenocortical disease, and has symptoms including agitation An important gene associated with Pigmented Nodular Adrenocortical Disease, Primary, 2 is PDE11A (Phosphodiesterase 11A). Affiliated tissues include cortex and skin, and related phenotypes are pigmented micronodular adrenocortical disease and increased circulating cortisol level

Related ID：

MALACARDS：PGM011

OMIM：610475

MESH：D003480