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1365683002: Non-syndromic bicoronal and metopic craniosynostosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5454296016 A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5454297013 A form of non-syndromic multisutural craniosynostosis characterized by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5454292019 Isolated bicoronal and metopic craniosynostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5454293012 Non-syndromic bilateral coronal and metopic suture synostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5454294018 Non-syndromic bicoronal and metopic craniosynostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5454295017 Non-syndromic bicoronal and metopic craniosynostosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Is a Bicoronal craniosynostosis true Inferred relationship Some
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Occurrence Congenital true Inferred relationship Some 1
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Finding site Structure of left coronal suture of skull true Inferred relationship Some 1
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Associated morphology Premature fusion true Inferred relationship Some 1
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Occurrence Congenital true Inferred relationship Some 2
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Finding site Structure of right coronal suture of skull true Inferred relationship Some 2
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Associated morphology Premature fusion true Inferred relationship Some 2
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Occurrence Congenital true Inferred relationship Some 3
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Finding site Structure of frontal suture of skull true Inferred relationship Some 3
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Associated morphology Premature fusion true Inferred relationship Some 3
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Occurrence Congenital true Inferred relationship Some 4
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Finding site Frontal bone structure true Inferred relationship Some 4
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Associated morphology Abnormal shape (morphologic abnormality) true Inferred relationship Some 4
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. Is a Interfrontal craniofaciosynostosis true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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