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716279002: Congenital duplication of nose (disorder)


Status: current, Defined. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3305374010 Congenital duplication of nose (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3305375011 Congenital duplication of nose en Synonym Active Case insensitive SNOMED CT core
3305376012 Polyrrhinia en Synonym Active Case insensitive SNOMED CT core
3305377015 Double nose en Synonym Active Case insensitive SNOMED CT core
3305378013 Polyrrhinia is an extremely rare, major congenital malformation with characteristic of complete duplication of the nose resulting in two fully developed noses often associated with choanal atresia, causing respiratory distress and necessitating surgical repair. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Polyrrhinia Pathological process Pathological developmental process true Inferred relationship Some 1
Polyrrhinia Is a Congenital anomaly of nose true Inferred relationship Some
Polyrrhinia Associated morphology Double structure true Inferred relationship Some 1
Polyrrhinia Occurrence Congenital true Inferred relationship Some 1
Polyrrhinia Finding site Nasal structure true Inferred relationship Some 1
Polyrrhinia Is a Diprosopus 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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