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253109005: Parietal encephalocele (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
376991013 Parietal encephalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643829012 Parietal encephalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
376991013 Parietal encephalocele en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
376991013 Parietal encephalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643829012 Parietal encephalocele (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
643829012 Parietal encephalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3423391001000116 Enzephalozele, parietale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
922351000172110 encéphalocèle pariétale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
922351000172110 encéphalocèle pariétale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3423391001000116 Enzephalozele, parietale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parietal encephalocele (disorder) Is a Encephalocele true Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Finding site Parietal lobe structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Finding site Parietal lobe structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Is a Disorder of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Is a Congenital and developmental anomalies of the nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Finding site Bone structure of head false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Parietal encephalocele (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Is a Cerebral herniation false Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Is a Congenital anomaly of cerebrum (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Is a Congenital anomaly of parietal bone (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Finding site Parietal bone structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Parietal encephalocele (disorder) Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Parietal encephalocele (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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