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93015002: Congenital anomaly of parietal bone (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
153847019 Congenital anomaly of parietal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836660018 Congenital anomaly of parietal bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
153847019 Congenital anomaly of parietal bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
153847019 Congenital anomaly of parietal bone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836660018 Congenital anomaly of parietal bone (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836660018 Congenital anomaly of parietal bone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4705951000241117 anomalie congénitale de l'os pariétal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4705951000241117 anomalie congénitale de l'os pariétal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of parietal bone (disorder) Is a Disorder of bone (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of parietal bone (disorder) Is a Congenital abnormality of skull and face bones (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of parietal bone (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of parietal bone (disorder) Finding site Parietal bone structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of parietal bone (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of parietal bone (disorder) Finding site Parietal bone structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of parietal bone (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of parietal bone (disorder) Is a Congenital anomaly of skull true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of parietal bone (disorder) Finding site Parietal bone structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of parietal bone (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of parietal bone (disorder) Is a Finding of head region true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Fronto-parietal craniofaciosynostosis Is a False Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Parieto-occipital craniosynostosis Is a False Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital abnormal fusion of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital abnormal shape of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital fenestration of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Lack of ossification of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Incomplete ossification of parietal bone Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies. Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Parietal encephalocele (disorder) Is a True Congenital anomaly of parietal bone (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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