| hyperinsulinisme door insulinereceptordeficiëntie (aandoening) | | hyperinsulinisme door insulinereceptordeficiëntie | | hyperinsulinisme door deficiëntie van insulinereceptor
| | Hyperinsulinism due to insulin receptor deficiency | | Hyperinsulinism due to INSR (insulin receptor) deficiency
| | A very rare autosomal dominant form of familial hyperinsulinism characterized clinically in the single reported family by postprandial hypoglycemia, fasting hyperinsulinemia, an elevated serum insulin-to-C peptide ratio and a variable age of onset. |
| | Id | 721235003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E16.1 | | Term | Overige gespecificeerde vormen van hypoglykemie |
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| SNOMED CT to Orphanet simple map | 263458 |
| SNOMED CT to ICD-10 extended map | | Target | E16.1 | | Rule | TRUE | | Advice | ALWAYS E16.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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