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1003429001: Focal cortical dysplasia type IIa (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4168225012 Focal cortical dysplasia type IIa en Synonym Active Initial character case insensitive SNOMED CT core
4168226013 Focal cortical dysplasia type IIa (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4166792010 Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells. en Definition Active Case sensitive SNOMED CT core
4166793017 Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells. 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 IIa Is a Localised cortical dysplasia true Inferred relationship Some
Focal cortical dysplasia type IIa Associated morphology Dysplasia true Inferred relationship Some 1
Focal cortical dysplasia type IIa Finding site Structure of cerebral cortex true Inferred relationship Some 1
Focal cortical dysplasia type IIa Occurrence Congenital true Inferred relationship Some 1
Focal cortical dysplasia type IIa Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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