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784350004: Craniorhiny (disorder)


Status: current, Not 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
3763736018 Craniorhiny (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763737010 Craniorhiny en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763738017 A rare frontonasal dysplasia malformation syndrome with characteristics of an oxycephalic skull with craniosynostosis, wide nose with anteverted nostrils, hirsutism at base of nose, agenesis of the nasolacrimal ducts and bilateral symmetrical nasolabial cysts on upper lip. Additional features may include hypertelorism. There have been no further descriptions in the literature since 1991. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763736018 Craniorhiny (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763737010 Craniorhiny en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763738017 A rare frontonasal dysplasia malformation syndrome with characteristics of an oxycephalic skull with craniosynostosis, wide nose with anteverted nostrils, hirsutism at base of nose, agenesis of the nasolacrimal ducts and bilateral symmetrical nasolabial cysts on upper lip. Additional features may include hypertelorism. There have been no further descriptions in the literature since 1991. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3432411001000112 Kraniorhinie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3432411001000112 Kraniorhinie 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
Craniorhiny (disorder) Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniorhiny (disorder) Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniorhiny (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniorhiny (disorder) Is a Congenital anomaly of bone and joint true Inferred relationship Existential restriction modifier (core metadata concept)
Craniorhiny (disorder) Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Craniorhiny (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniorhiny (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniorhiny (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniorhiny (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniorhiny (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniorhiny (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniorhiny (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniorhiny (disorder) Finding site Nasal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniorhiny (disorder) Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniorhiny (disorder) Is a Congenital anomaly of nose true Inferred relationship Existential restriction modifier (core metadata concept)
Craniorhiny (disorder) Is a Frontonasal dysplasia sequence true Inferred relationship Existential restriction modifier (core metadata concept)
Craniorhiny (disorder) Associated morphology Premature fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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