| 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 rare autosomal dominant form of familial hyperinsulinism characterized clinically by postprandial hypoglycemia, fasting hyperinsulinemia, and an elevated serum insulin-to-C peptide ratio, and a variable age of onset. |
| | Id | 721235003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to Orphanet simple map | 263458 |
| SNOMED CT to ICD-10 extended map | | Target | E16.1 | | Rule | TRUE | | Advice | ALWAYS E16.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
