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1003463004: Focal cortical dysplasia type I (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168310010 Focal cortical dysplasia type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4168311014 Focal cortical dysplasia type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
4168310010 Focal cortical dysplasia type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4168311014 Focal cortical dysplasia type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
6158571000241115 dysplasie corticale focale de type I fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6158571000241115 dysplasie corticale focale de type I fr Synonym (core metadata concept) Active Only initial character 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
Focal cortical dysplasia type I Is a Localised cortical dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Focal cortical dysplasia type I Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal cortical dysplasia type I Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal cortical dysplasia type I Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal cortical dysplasia type I Finding site Structure of cortex of temporal lobe 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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