| syndroom van telecanthus, hypertelorisme, strabisme en pes cavus (aandoening) | | syndroom van telecanthus, hypertelorisme, strabisme en pes cavus | | syndroom van telecanthus, hypertelorisme, strabismus en pes cavus
syndroom van Krauss-Herman-Holmes
Krauss-Herman-Holmes-syndroom
syndroom van telecanthus, hypertelorisme, scheelzien en holvoet
| | Telecanthus, hypertelorism, strabismus, pes cavus syndrome | | Telecanthus-hypertelorism-strabismus-pes cavus syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and other variable anomalies. It has been described in a father and his son. The son also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of the fingers, and radiographic findings including flared metaphyses of the long bones and osteopenia. |
| | Id | 733067006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q10.3 | | Term | Overige congenitale misvormingen van ooglid |
| Target | Q75.2 | | Term | Hypertelorisme |
| Target | H50.8 | | Term | Overig gespecificeerd strabismus |
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| SNOMED CT to ICD-10 extended map | | Target | Q87.8 | | Rule | TRUE | | Advice | ALWAYS Q87.8 | 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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