Autosomal dominant hereditary disorder	Autosomal dominant hereditary disorder	Digestive system hereditary disorder	Digestive system hereditary disorder	Familial disease	Familial disease	Hereditary disorder of endocrine system	Hereditary disorder of endocrine system	Hereditary metabolic disease	Hyperinsulinism	Hyperinsulinism
\|	\|	\|	\|	\|	\|	\|	\|	\|	\|	\|

Hyperinsulinism due to insulin receptor deficiency (disorder)
	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.
	hyperinsulinisme door insulinereceptordeficiëntie
	hyperinsulinisme door deficiëntie van insulinereceptor

Id	721235003
Status	Primitive

Due to

Insulin receptor defect

Due to

Insulin receptor defect

Finding site

Endocrine pancreatic structure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E16.1
Rule	TRUE
Advice	ALWAYS E16.1
Correlation	SNOMED CT source code to target map code correlation not specified