| | gemengd neuro-endocrien en niet-neuro-endocrien neoplasma van pancreas (aandoening) |  |  | gemengd neuro-endocrien en niet-neuro-endocrien neoplasma van pancreas |  |  | gemengd neuro-endocriene en niet-neuro-endocriene tumor van alvleesklierMiNEN van pancreas
 'mixed neuroendocrine-non neuroendocrine neoplasm' van pancreas
 
 |  |  | Mixed neuroendocrine-non neuroendocrine neoplasm of pancreas |  |  | Pancreatic mixed neuroendocrine-non-neuroendocrine neoplasmMiNEN (mixed neuroendocrine-non neuroendocrine neoplasm) of pancreas
 
 |  |  | A rare neuroendocrine neoplasm of pancreas characterized by morphologically recognizable neuroendocrine and non-neuroendocrine components, each constituting at least 30% of the tumor volume. Based on histopathology, mixed ductal- and mixed acinar-neuroendocrine carcinomas are distinguished. Patients usually present with unspecific symptoms related to tumor growth and/or metastasis, although occurrence of Zollinger-Ellison syndrome has been reported. Resectability of the tumor is the most important prognostic factor. | 
 | | Id | 1186735007 |  | Status | Defined | 
| SNOMED CT to Orphanet simple map | 506112 | 
| SNOMED CT to ICD-10 extended map |  | | Target | C25.9 |  | Rule | TRUE |  | Advice | ALWAYS C25.9 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE |  | Correlation | SNOMED CT source code to target map code correlation not specified | 
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