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95493003: Congenital retinoschisis (disorder)


Status: current, 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
158173012 Congenital retinoschisis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839658019 Congenital retinoschisis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
158173012 Congenital retinoschisis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
158173012 Congenital retinoschisis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839658019 Congenital retinoschisis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
839658019 Congenital retinoschisis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
556661000274115 Kongenitale Retinoschisis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627121000274111 Kongenitale Netzhautspaltung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
71521000077119 rétinoschisis congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
71521000077119 rétinoschisis congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
556661000274115 Kongenitale Retinoschisis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627121000274111 Kongenitale Netzhautspaltung 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 retinoschisis (disorder) Is a Retinoschisis true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Is a Congenital anomaly of retina false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Associated morphology Separation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital retinoschisis (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital retinoschisis (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinoschisis (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Associated morphology Separation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Associated morphology Separation true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital retinoschisis (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital retinoschisis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a False Congenital retinoschisis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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