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1003461002: Focal cortical dysplasia type II (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
4168306012 Focal cortical dysplasia type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4168307015 Focal cortical dysplasia type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4168591011 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168592016 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168306012 Focal cortical dysplasia type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4168307015 Focal cortical dysplasia type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4168591011 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168592016 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
6178591000241119 dysplasie corticale focale de type II fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6178591000241119 dysplasie corticale focale de type II 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 II Is a Localised cortical dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Focal cortical dysplasia type II Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal cortical dysplasia type II Finding site Cerebral cortex true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal cortical dysplasia type II Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal cortical dysplasia type II Pathological process (attribute) Pathological developmental process (qualifier value) 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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