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763830009: Oculomaxillofacial dysostosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3644152011 Oculomaxillofacial dysostosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644153018 Richieri Costa Gorlin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3644154012 Oculomaxillofacial dysostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644155013 A rare genetic bone developmental disorder with characteristics of short stature, orbital region and ocular abnormalities (e.g. asymmetric orbits, anophthalmia, down-slanted and S-shaped palpebral fissures, sparse eyebrows/eyelashes, abnormal eyelids, ectropion, symblepharon, corneal leukoma), abnormal nose (e.g. broad nasal root, bridge and tip, lateral deviation), malar hypoplasia, cleft lip/palate, and oblique facial clefts. Intellectual disability, microcephaly, micrognathia and limb anomalies (e.g. hemimelia, abnormal scapular girdle, brachydactyly, syndactyly, broad halluces) have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4149661000052111 okulomaxillofacial dysostos sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculomaxillofacial dysostosis (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Oculomaxillofacial dysostosis (disorder) Is a Dysostosis of bone of skull true Inferred relationship Some
Oculomaxillofacial dysostosis (disorder) Is a Short stature disorder true Inferred relationship Some
Oculomaxillofacial dysostosis (disorder) Associated morphology kongenital dysplasi false Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Occurrence Congenital true Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Finding site Bone structure of cranium true Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Associated morphology utvecklingsabnormitet false Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Finding site Face structure false Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Finding site Face structure true Inferred relationship Some 1
Oculomaxillofacial dysostosis (disorder) Occurrence Congenital true Inferred relationship Some 1
Oculomaxillofacial dysostosis (disorder) Finding site Bone structure of cranium false Inferred relationship Some 1
Oculomaxillofacial dysostosis (disorder) Associated morphology kongenital dysplasi false Inferred relationship Some 1
Oculomaxillofacial dysostosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculomaxillofacial dysostosis (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Oculomaxillofacial dysostosis (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Oculomaxillofacial dysostosis (disorder) Interprets Height / growth measure true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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