| syndroom van naevus sebaceus, malformaties van centraal zenuwstelsel, aplasia cutis congenita, limbale dermoïdcyste en naevus pigmentosus (aandoening) | | syndroom van naevus sebaceus, malformaties van centraal zenuwstelsel, aplasia cutis congenita, limbale dermoïdcyste en naevus pigmentosus | | SCALP-syndroom
syndroom van talgkliernaevus, CZS-malformaties, aplasia cutis congenita, limbaal dermoïd en pigmentvlek
| | SCALP syndrome | | Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome
| | A rare skin disease characterized by the association of sebaceous nevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic nevus and variable central nervous system abnormalities including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement. |
| | Id | 774208009 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q84.8 | | Term | Overige gespecificeerde congenitale misvormingen van huidadnexen |
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| SNOMED CT to Orphanet simple map | 370052 |
| SNOMED CT to ICD-10 extended map | | Target | Q84.8 | | Rule | TRUE | | Advice | ALWAYS Q84.8 | 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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