| syndroom van poikilodermie, alopecia, retrognathie en palatoschisis (aandoening) | | syndroom van poikilodermie, alopecia, retrognathie en palatoschisis | | syndroom van poikilodermie, alopecia, retrognathie en gespleten gehemelte
PARC-syndroom
| | Poikiloderma, alopecia, retrognathism, cleft palate syndrome | | PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome
PARC syndrome
| | PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990. |
| | Id | 771186004 | | 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 | 2825 |
| 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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