| amelogenesis imperfecta-gingivale hyperplasie-syndroom (aandoening) | | amelogenesis imperfecta-gingivale hyperplasie-syndroom | | amelogenesis imperfecta-tandvleeshyperplasie-syndroom syndroom van amelogenesis imperfecta en gingivale hyperplasie
| | Amelogenesis imperfecta and gingival hyperplasia syndrome | | Associates gingival fibromatosis with dental abnormalities including generalized thin hypoplastic amelogenesis imperfecta, intrapulpal calcifications and delay of tooth eruption. |
| | Id | 707607008 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | K00.5 | | Rule | TRUE | | Advice | ALWAYS K00.5 | | Correlation | SNOMED CT source code to target map code correlation not specified |
| Target | K06.1 | | Rule | TRUE | | Advice | ALWAYS K06.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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