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1003464005: Focal cortical dysplasia type Ia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4168312019 Focal cortical dysplasia type Ia en Synonym Active Initial character case insensitive SNOMED CT core
4168313012 Focal cortical dysplasia type Ia (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4168598017 Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type Ia presents late with mild symptoms and is more often seen in adults. Changes are present in the temporal lobe and are restricted to cortical dyslamination. en Definition Active Case sensitive SNOMED CT core
4168599013 Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type Ia presents late with mild symptoms and is more often seen in adults. Changes are present in the temporal lobe and are restricted to cortical dyslamination. 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 Ia Is a Localised cortical dysplasia true Inferred relationship Some
Focal cortical dysplasia type Ia Associated morphology Dysplasia true Inferred relationship Some 1
Focal cortical dysplasia type Ia Finding site Structure of cerebral cortex true Inferred relationship Some 1
Focal cortical dysplasia type Ia Occurrence Congenital true Inferred relationship Some 1
Focal cortical dysplasia type Ia 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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