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763317002: Isolated congenital syngnathia (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
3638525019 Isolated congenital maxillomandibular fusion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638526018 Isolated congenital syngnathia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638527010 Isolated congenital syngnathia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404008011 Isolated congenital syngnathia is a very rare developmental defect during embryogenesis disorder characterized by varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties which may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404009015 Isolated congenital syngnathia is a very rare developmental defect during embryogenesis disorder characterised by varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties which may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3638525019 Isolated congenital maxillomandibular fusion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638526018 Isolated congenital syngnathia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638527010 Isolated congenital syngnathia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638528017 A very rare developmental defect during embryogenesis with characteristics of varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties that may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404008011 Isolated congenital syngnathia is a very rare developmental defect during embryogenesis disorder characterized by varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties which may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404009015 Isolated congenital syngnathia is a very rare developmental defect during embryogenesis disorder characterised by varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties which may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431801001000115 Syngnathie, isolierte kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
987761000172116 syngnathie congénitale isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1012301000172110 fusion maxillo-mandibulaire congénitale isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
987761000172116 syngnathie congénitale isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1012301000172110 fusion maxillo-mandibulaire congénitale isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431801001000115 Syngnathie, isolierte kongenitale 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
Isolated congenital syngnathia (disorder) Is a Congenital anomaly of jaw (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Isolated congenital syngnathia (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated congenital syngnathia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated congenital syngnathia (disorder) Finding site Jaw region structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated congenital syngnathia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated congenital syngnathia (disorder) Is a Lesion of face false Inferred relationship Existential restriction modifier (core metadata concept)
Isolated congenital syngnathia (disorder) Associated morphology Abnormally fused structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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