Congenital anomaly of liver	Congenital nephropathy	Developmental hereditary disorder	Digestive system hereditary disorder	Glycogen storage disease	Hereditary nephropathy	Metabolic renal disease
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Glycogenosis with glucoaminophosphaturia (disorder)
	Glycogenosis with glucoaminophosphaturia
	Pseudo-phlorizin diabetes Renal glucose-losing syndrome Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome Fanconi-Bickel syndrome
	glycogeenstapelingsziekte type XI
	GSD type XI syndroom van Fanconi-Bickel

Id	61598006
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Liver structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site	Kidney structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E74.0
Rule	TRUE
Advice	ALWAYS E74.0
Correlation	SNOMED CT source code to target map code correlation not specified