| syndroom van niet doorkomen van tanden, hypoplasie van maxilla en genu valgum (aandoening) | | syndroom van niet doorkomen van tanden, hypoplasie van maxilla en genu valgum | | syndroom van niet doorkomen van tanden, hypoplasie van maxillaire en genu valgum
syndroom van Stoelinga-De Koomen-Davis
| | Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome | | Stoelinga de Koomen Davis syndrome
| | An extremely rare syndrome with characteristics of multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. Consanguinity in the family suggested autosomal recessive inheritance. |
| | Id | 723442008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | K00.6 | | Term | Stoornissen in tanddoorbraak |
| Target | K07.0 | | Term | Grove afwijkingen van afmeting van kaak |
| Target | Q74.1 | | Term | Congenitale misvorming van knie |
|
| SNOMED CT to Orphanet simple map | 2972 |
| SNOMED CT to ICD-10 extended map | | Target | K00.6 | | Rule | TRUE | | Advice | ALWAYS K00.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
| Target | K07.0 | | Rule | TRUE | | Advice | ALWAYS K07.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
| Target | Q74.1 | | Rule | TRUE | | Advice | ALWAYS Q74.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
