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1003463004: Focal cortical dysplasia type I (disorder)


Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168310010 Focal cortical dysplasia type I en Synonym Active Initial character case insensitive SNOMED CT core
4168311014 Focal cortical dysplasia type I (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4168589015 Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type I presents late with mild symptoms and is more often seen in adults. Changes are present in the temporal lobe. en Definition Active Case sensitive SNOMED CT core
4168590012 Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type I presents late with mild symptoms and is more often seen in adults. Changes are present in the temporal lobe. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Focal cortical dysplasia type I Is a Localised cortical dysplasia true Inferred relationship Some
Focal cortical dysplasia type I Associated morphology Dysplasia true Inferred relationship Some 1
Focal cortical dysplasia type I Occurrence Congenital true Inferred relationship Some 1
Focal cortical dysplasia type I Pathological process Pathological developmental process true Inferred relationship Some 1
Focal cortical dysplasia type I Finding site Structure of cortex of temporal lobe true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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