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719274008: dysplasie micronodulaire pigmentée des surrénales (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3315796012 Primary pigmented nodular adrenocortical disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
753951000241119 dysplasie micronodulaire pigmentée des surrénales (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
887251000172119 maladie adrénocorticale nodulaire pigmentée primaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
986111000172115 dysplasie micronodulaire pigmentée des surrénales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary pigmented nodular adrenocortical disease (disorder) est un(e) (attribut) Micronodular adrenal hyperplasia true Inferred relationship Some
Primary pigmented nodular adrenocortical disease (disorder) morphologie associée (attribut) Micronodular hyperplasia (morphologic abnormality) true Inferred relationship Some 1
Primary pigmented nodular adrenocortical disease (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Primary pigmented nodular adrenocortical disease (disorder) est un(e) (attribut) Adrenocortical hyperplasia false Inferred relationship Some
Primary pigmented nodular adrenocortical disease (disorder) est un(e) (attribut) Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
Primary pigmented nodular adrenocortical disease (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 1
Primary pigmented nodular adrenocortical disease (disorder) localisation d'une constatation (attribut) cortex surrénalien true Inferred relationship Some 1
Primary pigmented nodular adrenocortical disease (disorder) morphologie associée (attribut) Hyperplasia (morphologic abnormality) false Inferred relationship Some 2
Primary pigmented nodular adrenocortical disease (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Primary pigmented nodular adrenocortical disease (disorder) localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

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