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237680001: Corticotroph hyperplasia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356223013 Corticotroph hyperplasia en Synonym Active Case insensitive SNOMED CT core
626442016 Corticotroph hyperplasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Corticotroph hyperplasia Finding site Structure of distal part of pituitary false Inferred relationship Some 1
Corticotroph hyperplasia Associated morphology Hyperplasia false Inferred relationship Some 1
Corticotroph hyperplasia Associated morphology Hyperplasia true Inferred relationship Some 1
Corticotroph hyperplasia Finding site Structure of distal part of pituitary true Inferred relationship Some 1
Corticotroph hyperplasia Finding site Pars anterior of pituitary gland false Inferred relationship Some
Corticotroph hyperplasia Finding site Entire endocrine gonad false Inferred relationship Some
Corticotroph hyperplasia Is a Anterior pituitary hyperplasia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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