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719274008: Primary pigmented nodular adrenocortical disease (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315785016 Primary pigmented nodular adrenocortical disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3315796012 Primary pigmented nodular adrenocortical disease en Synonym Active Case insensitive SNOMED CT core
3315797015 Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal sized adrenal glands containing multiple small cortical pigmented nodules. A substantial proportion of patients present during early childhood (2-3 years). More than 90% of reported cases of PPNAD occur as one of the manifestations of Carney complex. The condition is inherited in an autosomal dominant manner and can be associated with mutations in the PRKAR1A, PDE11A and PDE8B genes. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary pigmented nodular adrenocortical disease Is a Micronodular adrenal hyperplasia true Inferred relationship Some
Primary pigmented nodular adrenocortical disease Associated morphology Micronodular hyperplasia true Inferred relationship Some 1
Primary pigmented nodular adrenocortical disease Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Primary pigmented nodular adrenocortical disease Is a Adrenocortical hyperplasia false Inferred relationship Some
Primary pigmented nodular adrenocortical disease Is a Hereditary disorder of endocrine system true Inferred relationship Some
Primary pigmented nodular adrenocortical disease Associated morphology Hyperplasia false Inferred relationship Some 1
Primary pigmented nodular adrenocortical disease Finding site Adrenal cortex structure true Inferred relationship Some 1
Primary pigmented nodular adrenocortical disease Associated morphology Hyperplasia false Inferred relationship Some 2
Primary pigmented nodular adrenocortical disease Occurrence Congenital false Inferred relationship Some 2
Primary pigmented nodular adrenocortical disease Finding site Adrenal cortex structure false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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