Pigmented Nodular Adrenocortical Disease, Primary, 1 (PPNAD1)

Alias:

Ppnad1

Adrenocortical Disease, Nodular, Pigmented, Primary, Type 1

Pigmented Micronodular Adrenocortical Disease, Primary, 1

Primary Pigmented Micronodular Adrenocortical Disease 1

Primary Pigmented Nodular Adrenocortical Disease 1

Primary Pigmented Nodular Adrenocortical Disease-1

Adrenocortical Nodular Dysplasia, Primary

Cushing Syndrome, Adrenal, Due to Ppnad1

Nodular Primary Adrenocortical Dysplasia

Adrenal Cushing Syndrome Due to Ppnad1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Pigmented Nodular Adrenocortical Disease, Primary, 1, also known as ppnad1, is related to primary pigmented nodular adrenocortical disease and basophil adenoma, and has symptoms including agitation An important gene associated with Pigmented Nodular Adrenocortical Disease, Primary, 1 is PRKAR1A (Protein Kinase CAMP-Dependent Type I Regulatory Subunit Alpha), and among its related pathways/superpathways are Beta-Adrenergic Signaling and NFAT and Cardiac Hypertrophy. Affiliated tissues include cortex and bone, and related phenotypes are increased circulating cortisol level and increased urinary cortisol level

Related ID：

MALACARDS：PGM021

OMIM：610489

MESH：D003480