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1231209008: Congenital meningocele of orbit (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5071870013 Congenital meningocele of orbit (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5072976016 Congenital orbital meningocele en Synonym Active Entire term case insensitive SNOMED CT core module
5073552013 Congenital meningocele of orbit en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital meningocele of orbit Is a Disorder of bony orbit true Inferred relationship Existential restriction modifier
Congenital meningocele of orbit Is a Congenital anomaly of skull true Inferred relationship Existential restriction modifier
Congenital meningocele of orbit Is a Congenital anomaly of orbit proper true Inferred relationship Existential restriction modifier
Congenital meningocele of orbit Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital meningocele of orbit Finding site Bony orbit structure true Inferred relationship Existential restriction modifier 1
Congenital meningocele of orbit Associated morphology Hernial opening true Inferred relationship Existential restriction modifier 1
Congenital meningocele of orbit Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital meningocele of orbit Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital meningocele of orbit Finding site Structure of orbital meninges true Inferred relationship Existential restriction modifier 2
Congenital meningocele of orbit Associated morphology Herniated structure true Inferred relationship Existential restriction modifier 2
Congenital meningocele of orbit Is a Congenital meningocele true Inferred relationship Existential restriction modifier
Congenital meningocele of orbit Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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