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874814009: Micronodular hyperplasia (morphologic abnormality)

Status: current, Not 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
3982911017 Micronodular hyperplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3982912012 Micronodular hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Micronodular hyperplasia (morphologic abnormality) Is a Nodular hyperplasia true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Micronodular adrenal hyperplasia Associated morphology True Micronodular hyperplasia (morphologic abnormality) Inferred relationship Some 1
dysplasie micronodulaire pigmentée des surrénales Associated morphology False Micronodular hyperplasia (morphologic abnormality) Inferred relationship Some 1
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. Associated morphology True Micronodular hyperplasia (morphologic abnormality) Inferred relationship Some 1
Carney complex-associated-primary pigmented nodular adrenocortical disease (disorder) Associated morphology True Micronodular hyperplasia (morphologic abnormality) Inferred relationship Some 1
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. Associated morphology True Micronodular hyperplasia (morphologic abnormality) Inferred relationship Some 1
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. Associated morphology True Micronodular hyperplasia (morphologic abnormality) Inferred relationship Some 2

This concept is not in any reference sets

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