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897593008: Congenital disruption of omphalomesenteric artery (disorder)


Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4034404012 Congenital disruption of omphalomesenteric artery en Synonym Active Case insensitive SNOMED CT core
4034405013 Vitelline artery disruption en Synonym Active Case insensitive SNOMED CT core
4034406014 Congenital disruption of omphalomesenteric artery (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
Congenital disruption of omphalomesenteric artery Is a Disorder of embryonic structure true Inferred relationship Some
Congenital disruption of omphalomesenteric artery Finding site Structure of omphalomesenteric artery true Inferred relationship Some 1
Congenital disruption of omphalomesenteric artery Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital disruption of omphalomesenteric artery Associated morphology Disruption true Inferred relationship Some 1
Congenital disruption of omphalomesenteric artery Is a Congenital anomaly of artery true Inferred relationship Some
Congenital disruption of omphalomesenteric artery Occurrence Congenital true Inferred relationship Some 1
Congenital disruption of omphalomesenteric artery Is a Injury of artery true Inferred relationship Some
Congenital disruption of omphalomesenteric artery Is a Soft tissue lesion true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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