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204181009: Congenital retinal fold (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
313095011 Congenital retinal fold en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
589373011 Congenital retinal fold (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
313095011 Congenital retinal fold en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
313095011 Congenital retinal fold en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
589373011 Congenital retinal fold (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
589373011 Congenital retinal fold (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
633591000274110 Kongenitale Netzhautfalte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
633601000274115 Kongenitale Retinafalte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4879521000241111 pli rétinien congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4879521000241111 pli rétinien congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
633591000274110 Kongenitale Netzhautfalte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
633601000274115 Kongenitale Retinafalte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Congenital retinal fold Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinal fold Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinal fold Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinal fold Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinal fold Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinal fold Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinal fold Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinal fold Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinal fold Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinal fold Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinal fold Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinal fold Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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