| melanosis diffusa congenita (aandoening) | | melanosis diffusa congenita | | melanosis universalis hereditaria
familiaire progressieve hyperpigmentatie
| | Familial progressive hyperpigmentation | | Melanosis diffusa congenita
Melanosis universalis hereditaria
Universal melanosis
| | Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder. |
| | Id | 715630006 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | L81.4 | | Term | Overige vormen van hyperpigmentatie door melanine |
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| SNOMED CT to Orphanet simple map | 79146 |
| SNOMED CT to ICD-10 extended map | | Target | L81.4 | | Rule | TRUE | | Advice | ALWAYS L81.4 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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