Telecanthus, hypertelorism, strabismus, pes cavus syndrome (disorder) | | Telecanthus, hypertelorism, strabismus, pes cavus syndrome | | Syndrome with characteristics of 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. Radiographic findings including flared metaphyses of the long bones and osteopenia. | | syndroom van telecanthus, hypertelorisme, strabisme en pes cavus | | Krauss-Herman-Holmes-syndroom syndroom van telecanthus, hypertelorisme, scheelzien en holvoet syndroom van telecanthus, hypertelorisme, strabismus en pes cavus syndroom van Krauss-Herman-Holmes
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| Id | 733067006 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | Q10.3 | Rule | TRUE | Advice | ALWAYS Q10.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | Q75.2 | Rule | TRUE | Advice | ALWAYS Q75.2 | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | H50.8 | Rule | TRUE | Advice | ALWAYS H50.8 | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | Q66.7 | Rule | TRUE | Advice | ALWAYS Q66.7 | Correlation | SNOMED CT source code to target map code correlation not specified |
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