FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

204181009: Congenital retinal fold (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
313095011 Congenital retinal fold en Synonym Active Entire term case insensitive SNOMED CT core module
589373011 Congenital retinal fold (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital retinal fold Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier
Congenital retinal fold Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital retinal fold Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Congenital retinal fold Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Congenital retinal fold Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital retinal fold Finding site Retinal structure false Inferred relationship Existential restriction modifier 1
Congenital retinal fold Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital retinal fold Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital retinal fold Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital retinal fold Finding site Retinal structure false Inferred relationship Existential restriction modifier 2
Congenital retinal fold Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital retinal fold Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Congenital retinal fold Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start