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715422002: Craniotelencephalic dysplasia (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3302564015 Craniotelencephalic dysplasia en Synonym Active Case insensitive SNOMED CT core
3302565019 Characterized by frontal encephalocele, craniosynostosis, and developmental delay. en Definition Active Case sensitive SNOMED CT core
3302566018 Characterised by frontal encephalocoele, craniosynostosis, and developmental delay. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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