Pigmented Nodular Adrenocortical Disease, Primary, 4 (PPNAD4)

Alias:

Chromosome 19p13 Duplication Syndrome

Ppnad4

Adrenocortical Disease, Nodular, Pigmented, Primary, Type 4

Primary Pigmented Nodular Adrenocortical Disease 4

Cushing Syndrome, Adrenal, Due to Ppnad4

Adrenal Cushing Syndrome Due to Ppnad4

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Pigmented Nodular Adrenocortical Disease, Primary, 4, is also known as chromosome 19p13 duplication syndrome, and has symptoms including cushingoid facies An important gene associated with Pigmented Nodular Adrenocortical Disease, Primary, 4 is PRKACA (Protein Kinase CAMP-Activated Catalytic Subunit Alpha). Affiliated tissues include cortex and skin, and related phenotypes are emotional lability and depression

Related ID：

MALACARDS：PGM022

OMIM：615830

MESH：D003480