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438583008: Congenital bilateral perisylvian syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2786814010 Congenital bilateral perisylvian syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2793048018 Congenital bilateral perisylvian syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2786814010 Congenital bilateral perisylvian syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2786814010 Congenital bilateral perisylvian syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2793048018 Congenital bilateral perisylvian syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2793048018 Congenital bilateral perisylvian syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5325921000241113 syndrome périsylvien congénital bilatéral fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5325921000241113 syndrome périsylvien congénital bilatéral fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital bilateral perisylvian syndrome (disorder) Is a Microgyria false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital bilateral perisylvian syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital bilateral perisylvian syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital bilateral perisylvian syndrome (disorder) Finding site Gyrus of brain false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital bilateral perisylvian syndrome (disorder) Finding site Gyrus of brain true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital bilateral perisylvian syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital bilateral perisylvian syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital bilateral perisylvian syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital bilateral perisylvian syndrome (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital bilateral perisylvian syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital bilateral perisylvian syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital bilateral perisylvian syndrome (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital bilateral perisylvian syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital bilateral perisylvian syndrome (disorder) Finding site Gyrus of brain false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital bilateral perisylvian syndrome (disorder) Is a Bilateral polymicrogyria (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital bilateral perisylvian syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital bilateral perisylvian syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital bilateral perisylvian syndrome (disorder) Associated morphology Abnormal smallness (morphologic abnormality) 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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