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449790007: Orofacial cleft (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2012. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2912837010 Orofacial cleft (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2912956018 Orofacial cleft en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
358631000195114 schisi oro-facciale it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5377401000241118 fente orofaciale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
22191001000114 Orofaziale Spalte de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


143 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Orofacial cleft (disorder) Associated morphology anomalie congénitale false Inferred relationship Some 1
Orofacial cleft (disorder) Is a Congenital abnormality of oral cavity false Inferred relationship Some
Orofacial cleft (disorder) Finding site Oral cavity structure false Inferred relationship Some 1
Orofacial cleft (disorder) Associated morphology anomalie congénitale false Inferred relationship Some 2
Orofacial cleft (disorder) Finding site Structure of internal part of mouth false Inferred relationship Some 2
Orofacial cleft (disorder) Occurrence Congenital true Inferred relationship Some 1
Orofacial cleft (disorder) Associated morphology anomalie du développement false Inferred relationship Some 1
Orofacial cleft (disorder) Finding site Structure of internal part of mouth false Inferred relationship Some 1
Orofacial cleft (disorder) Is a Cleft face false Inferred relationship Some
Orofacial cleft (disorder) Finding site Structure of subregion of head true Inferred relationship Some 1
Orofacial cleft (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 1
Orofacial cleft (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Orofacial cleft (disorder) Is a Finding of head region true Inferred relationship Some
Orofacial cleft (disorder) Is a Craniofacial cleft (disorder) true Inferred relationship Some
Orofacial cleft (disorder) Finding site Bone structure of head false Inferred relationship Some 2
Orofacial cleft (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 2
Orofacial cleft (disorder) Occurrence Congenital false Inferred relationship Some 2
Orofacial cleft (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Cleft lip Is a True Orofacial cleft (disorder) Inferred relationship Some
Cleft palate Is a True Orofacial cleft (disorder) Inferred relationship Some
This syndrome is characterized by cardiac arrhythmias (ventricular extrasystoles manifesting as bigeminy or multifocal tachycardia with syncopal episodes), perodactyly (hypoplasia and/or agenesis of the distal phalanges of the toes) and Pierre-Robin sequence. Is a True Orofacial cleft (disorder) Inferred relationship Some
A rare ectodermal dysplasia syndrome characterized by severe arthrogryposis, multiple ectodermal dysplasia features, cleft lip/palate, facial dysmorphism, growth deficiency and a moderate delay of psychomotor development. Ectodermal dysplasia manifestations include sparse, brittle and hypopigmented hair, xerosis, multiple nevi, small conical shaped teeth and hypodontia, and facial dysmorphism with blepharophimosis, deep-set eyes and micrognathia. Is a True Orofacial cleft (disorder) Inferred relationship Some
Kapur-Toriello syndrome is an extremely rare syndrome characterized by facial dysmorphism, severe intellectual deficiency, cardiac and intestinal anomalies, and growth retardation. Is a True Orofacial cleft (disorder) Inferred relationship Some
Cleft of alveolar ridge (disorder) Is a True Orofacial cleft (disorder) Inferred relationship Some
Cleft mandible Is a True Orofacial cleft (disorder) Inferred relationship Some
Congenital macrostomia Is a True Orofacial cleft (disorder) Inferred relationship Some
A rare congenital nose and cavum anomaly characterized by clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia; other malformations such as hypertelorbitism and midline clefts of the lip may also be associated. Is a False Orofacial cleft (disorder) Inferred relationship Some
Cleft tongue Is a True Orofacial cleft (disorder) Inferred relationship Some
Insertion of nasoalveolar molding appliance Has focus True Orofacial cleft (disorder) Inferred relationship Some 2
Insertion of cleft lip or palate strapping appliance Has focus True Orofacial cleft (disorder) Inferred relationship Some 2
Fitting of cleft lip or palate strapping appliance (procedure) Has focus True Orofacial cleft (disorder) Inferred relationship Some 2

This concept is not in any reference sets

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