| geïsoleerde congenitale synechie (aandoening) | | geïsoleerde congenitale synechie | | Isolated congenital syngnathia | | Isolated congenital maxillomandibular fusion
| | 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. |
| | Id | 763317002 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q67.4 | | Term | Overige congenitale misvormingen van schedel, aangezicht en kaak |
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| SNOMED CT to Orphanet simple map | 141214 |
| SNOMED CT to ICD-10 extended map | | Target | Q67.4 | | Rule | TRUE | | Advice | ALWAYS Q67.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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