| syndroom van craniofaciale, digitale en genitale afwijkingen (aandoening) | | syndroom van craniofaciale, digitale en genitale afwijkingen | | syndroom van Harrod
Harrod-syndroom
cranio-facio-digito-genitaal-syndroom
syndroom van craniofaciale, digitale en genitale anomalieën
| | problemen met je schedel, gezicht, vingers, tenen en geslachtsdelen |  | Dit betekent dat je schedel, gezicht, vingers, tenen en geslachtsdelen er anders uitzien dan normaal. Je bent hiermee geboren. | | Harrod syndrome | | Craniofacial digital and genital anomalies syndrome
Cranio-facio-digito-genital syndrome
| | A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive. |
| | Id | 716089008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.4 | | Term | Syndroom van Marfan |
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| SNOMED CT to Orphanet simple map | 2115 |
| SNOMED CT to ICD-10 extended map | | Target | Q87.0 | | Rule | TRUE | | Advice | ALWAYS Q87.0 | 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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