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237779006: Micronodular adrenal hyperplasia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356343016 Micronodular adrenal hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626556016 Micronodular adrenal hyperplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5020301000241111 hyperplasie surrénalienne micronodulaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Micronodular adrenal hyperplasia Is a Nodular adrenal cortex false Inferred relationship Some
Micronodular adrenal hyperplasia Is a Adrenocortical hyperplasia false Inferred relationship Some
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Associated morphology Nodule false Inferred relationship Some 2
Micronodular adrenal hyperplasia Associated morphology Glandular and stromal hyperplasia false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure true Inferred relationship Some 1
Micronodular adrenal hyperplasia Finding site Adrenal cortex structure false Inferred relationship Some 2
Micronodular adrenal hyperplasia Associated morphology Micronodular hyperplasia (morphologic abnormality) true Inferred relationship Some 1
Micronodular adrenal hyperplasia Is a Nodular hyperplasia of adrenal cortex (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Pigmented micronodular adrenal hyperplasia Is a False Micronodular adrenal hyperplasia Inferred relationship Some
dysplasie micronodulaire pigmentée des surrénales Is a False Micronodular adrenal hyperplasia Inferred relationship Some
A rare adrenocortical nodular disease characterized by increased to normal sized adrenal glands containing multiple small (less than 1 cm in diameter) cortical pigmented (lipofuscin) nodules, surrounded by internodular adrenocortical atrophy. It is typically associated with the development of a form of adrenal Cushing syndrome (CS). Rarely, it has been associated with adrenal macronodules. Whilst PRKAR1A variants are associated with CNC (Carney complex), the mutation c.709-7del6 is mostly associated with i-PPNAD. Other mutations associated with i-PPNAD include PRKACA (germline copy-number gains), PDE11A and PDE8B genes, although these are rare. Is a True Micronodular adrenal hyperplasia Inferred relationship Some
Carney complex-associated-primary pigmented nodular adrenocortical disease (disorder) Is a True Micronodular adrenal hyperplasia Inferred relationship Some
A rare adrenocortical nodular disease characterized by bilateral, multiple micronodules (<1 cm), typically associated with endogenous Cushing syndrome, that occurs predominantly in children and young adults (females in majority). Pigmentation and inter-nodular adrenal cortical atrophy (histological findings present in primary pigmented nodular adrenocortical disease) are generally absent. Is a True Micronodular adrenal hyperplasia Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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