| X-gebonden dominante chondrodysplasie Chassaing-Lacombe-type (aandoening) | | X-gebonden dominante chondrodysplasie Chassaing-Lacombe-type | | X-gebonden dominante dyschondroplasie Chassaing-Lacombe-type
X-gebonden dominante chondrodysplasie-hydrocefalie-microftalmie
| | X-linked dominant chondrodysplasia Chassaing Lacombe type | | X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males. |
| | Id | 719837003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.8 | | Term | Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd |
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| SNOMED CT to Orphanet simple map | 163966 |
| 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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