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18389004: Microcolon (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
31039019 Microcolon en Synonym Active Case insensitive SNOMED CT core
745806015 Microcolon (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
Microcolon Pathological process Pathological developmental process true Inferred relationship Some 1
Microcolon Occurrence Congenital true Inferred relationship Some 1
Microcolon Is a Congenital anomaly of large intestine true Inferred relationship Some
Microcolon Is a Congenital functional disorders of the colon true Inferred relationship Some
Microcolon Occurrence Congenital false Inferred relationship Some
Microcolon Finding site Colon structure true Inferred relationship Some 1
Microcolon Associated morphology Congenital smallness true Inferred relationship Some 1
Microcolon Occurrence Congenital false Inferred relationship Some 2
Microcolon Finding site Colon structure false Inferred relationship Some 2
Microcolon Associated morphology Congenital smallness false Inferred relationship Some 1
Microcolon Occurrence Congenital false Inferred relationship Some
Microcolon Finding site Colon structure false Inferred relationship Some 1

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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