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14821001: Situs ambiguus (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
25183010 Situs ambiguus en Synonym Active Entire term case insensitive SNOMED CT core module
741217018 Situs ambiguus (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2646362013 Heterotaxy en Synonym Active Entire term case insensitive SNOMED CT core module
2646363015 Heterotaxis en Synonym Active Entire term case insensitive SNOMED CT core module
2646364014 Heterotaxia en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Situs ambiguus Is a Regional congenital anomaly false Inferred relationship Existential restriction modifier
Situs ambiguus Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Situs ambiguus Is a Congenital malformation true Inferred relationship Existential restriction modifier
Situs ambiguus Is a Viscus structure finding true Inferred relationship Existential restriction modifier
Situs ambiguus Finding site Structure of viscus true Inferred relationship Existential restriction modifier 1
Situs ambiguus Associated morphology Malposition true Inferred relationship Existential restriction modifier 1
Situs ambiguus Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Polysplenia heterotaxy syndrome Is a True Situs ambiguus Inferred relationship Existential restriction modifier
Cardiac anomaly and heterotaxy syndrome Is a True Situs ambiguus Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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