| neonatale sclerodermie (aandoening) | | neonatale sclerodermie | | systemische sclerose bij neonaat
sclerodermie bij pasgeborene
| | Neonatal scleroderma | | A rare secondary neonatal autoimmune disease characterized by neonatal onset of erythematous skin lesions with a linear appearance that gradually become indurated and hyperpigmented and progressively present skin atrophy. Positive serum antibodies (in particular antinuclear antibodies and/or rheumatoid factor) may be associated. |
| | Id | 774080007 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | P83.8 | | Term | Overige gespecificeerde huidaandoeningen specifiek voor foetus en pasgeborene |
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| SNOMED CT to Orphanet simple map | 398127 |
| SNOMED CT to ICD-10 extended map | | Target | P83.8 | | Rule | TRUE | | Advice | ALWAYS P83.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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