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715422002: Craniotelencephalic dysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302563014 Craniotelencephalic dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302564015 Craniotelencephalic dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400874016 Craniotelencephalic dysplasia is an extremely rare, genetic developmental defect during embryogenesis syndrome characterized by craniosynostosis with frontal encephalocele and various additional brain anomalies (severe hydrocephalus, agenesis of the corpus callosum, lissencephaly and polymicrogyria, parenchymal cysts, septo-optic dysplasia) resulting in marked cerebral dysfunction, seizures and very severe psychomotor delay. There have been no further descriptions in the literature since 1983. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400875015 Craniotelencephalic dysplasia is an extremely rare, genetic developmental defect during embryogenesis syndrome characterised by craniosynostosis with frontal encephalocele and various additional brain anomalies (severe hydrocephalus, agenesis of the corpus callosum, lissencephaly and polymicrogyria, parenchymal cysts, septo-optic dysplasia) resulting in marked cerebral dysfunction, seizures and very severe psychomotor delay. There have been no further descriptions in the literature since 1983. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Craniotelencephalic dysplasia (disorder) Is a Lissencephaly true Inferred relationship Some
Craniotelencephalic dysplasia (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Craniotelencephalic dysplasia (disorder) Occurrence Congenital false Inferred relationship Some 2
Craniotelencephalic dysplasia (disorder) Finding site Structure of central nervous system (body structure) false Inferred relationship Some 2
Craniotelencephalic dysplasia (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 3
Craniotelencephalic dysplasia (disorder) Finding site Brain structure false Inferred relationship Some 3
Craniotelencephalic dysplasia (disorder) Occurrence Congenital true Inferred relationship Some 1
Craniotelencephalic dysplasia (disorder) Finding site Brain structure true Inferred relationship Some 1
Craniotelencephalic dysplasia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Craniotelencephalic dysplasia (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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