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253784007: Hyperganglionosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
377868019 Hyperganglionosis en Synonym Active Case insensitive SNOMED CT core
644585019 Hyperganglionosis (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
Hyperganglionosis Occurrence Congenital true Inferred relationship Some 1
Hyperganglionosis Pathological process Pathological developmental process true Inferred relationship Some 1
Hyperganglionosis Is a Congenital anomaly of large intestine true Inferred relationship Some
Hyperganglionosis Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Hyperganglionosis Associated morphology Congenital anomaly false Inferred relationship Some 1
Hyperganglionosis Finding site Structure of large intestine false Inferred relationship Some 1
Hyperganglionosis Occurrence Congenital false Inferred relationship Some
Hyperganglionosis Finding site Colon structure true Inferred relationship Some 1
Hyperganglionosis Associated morphology Congenital anomaly false Inferred relationship Some 1
Hyperganglionosis Occurrence Congenital false Inferred relationship Some 2
Hyperganglionosis Finding site Colon structure false Inferred relationship Some 2
Hyperganglionosis Finding site Colon structure false Inferred relationship Some 1
Hyperganglionosis Occurrence Congenital false Inferred relationship Some
Hyperganglionosis Is a Congenital functional disorders of the colon 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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