| maculopapuleuze cutane mastocytose (aandoening) | | maculopapuleuze cutane mastocytose | | Maculopapular cutaneous mastocytosis | | A form of cutaneous mastocytosis (CM) characterized by the presence of multiple hyperpigmented macules, papules or nodules associated with abnormal accumulation of mast cells in the skin. Most patients present in infancy or childhood, but onset may also occur in adulthood. Mutations in the KIT gene (4q11-q12) have been identified however this mutation is rare in the pediatric population and the etiology and pathogenesis in these cases remains to be determined. The disease generally occurs sporadically but rare familial cases have been reported. |
| | Id | 1332134000 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | Q82.2 | | Rule | TRUE | | Advice | ALWAYS Q82.2 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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