Autosomal dominant hereditary disorder	Autosomal dominant hereditary disorder	Congenital disease	Digestive system hereditary disorder	Digestive system hereditary disorder	Hereditary disorder of endocrine system	Hereditary disorder of endocrine system	Hereditary metabolic disease	Hyperinsulinism	Hyperinsulinism
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Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder)
	Hyperinsulinism due to HNF1A deficiency
	Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency
	A form of diazoxide-sensitive diffuse hyperinsulinism, characterized by transient or persistent hyperinsulinemic hypoglycemia in infancy that is responsive to diazoxide, evolving in to maturity-onset diabetes of the young subtype 1 later in life.
	hyperinsulinisme door deficiëntie van 'hepatocyte nuclear factor'-1-alfa
	hyperinsulinisme door HNF-1-alfa-deficiëntie hyperinsulinisme door 'hepatocyte nuclear factor'-1-alfa-deficiëntie

Id	721234004
Status	Primitive

Finding site	Endocrine pancreatic structure
Occurrence	Congenital

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