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204181009: Congenital retinal fold (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
313095011 Congenital retinal fold en Synonym Active Case insensitive SNOMED CT core
589373011 Congenital retinal fold (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 retinal fold Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Congenital retinal fold Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital retinal fold Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital retinal fold Is a Congenital anomaly of retina true Inferred relationship Some
Congenital retinal fold Finding site Retinal structure false Inferred relationship Some 1
Congenital retinal fold Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital retinal fold Occurrence Congenital false Inferred relationship Some 2
Congenital retinal fold Associated morphology Developmental abnormality false Inferred relationship Some 2
Congenital retinal fold Finding site Retinal structure false Inferred relationship Some 2
Congenital retinal fold Occurrence Congenital true Inferred relationship Some 1
Congenital retinal fold Occurrence Congenital false Inferred relationship Some
Congenital retinal fold Finding site Structure of nervous system false Inferred relationship Some
Congenital retinal fold Finding site Retinal structure true 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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