The following pages link to Hyperinsulinemic hypoglycemia
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Pseudoxanthoma elasticum (links | edit)
- African iron overload (links | edit)
- Nonsyndromic deafness (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Progressive familial intrahepatic cholestasis (links | edit)
- Acrodermatitis enteropathica (links | edit)
- Testicular microlithiasis (links | edit)
- Vesicular monoamine transporter 1 (links | edit)
- Stargardt disease (links | edit)
- Tangier disease (links | edit)
- Sitosterolemia (links | edit)
- Solute carrier family (links | edit)
- Pyruvate carboxylase deficiency (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Hyperoxaluria (links | edit)
- Sucrose intolerance (links | edit)
- Episodic ataxia (links | edit)
- Triosephosphate isomerase deficiency (links | edit)
- Thyroid dyshormonogenesis (links | edit)
- Galactokinase deficiency (links | edit)
- Aldolase A deficiency (links | edit)
- Glycogen storage disease type VI (links | edit)
- Arterial tortuosity syndrome (links | edit)
- Renal glycosuria (links | edit)
- Pentosuria (links | edit)
- Galactose epimerase deficiency (links | edit)
- Essential fructosuria (links | edit)
- Galactose-1-phosphate uridylyltransferase deficiency (links | edit)
- Allan–Herndon–Dudley syndrome (links | edit)
- GLUT1 deficiency (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Primary hyperoxaluria (links | edit)
- Hexokinase deficiency (links | edit)
- Galactosemic cataract (links | edit)
- Glycogen storage disease type IX (links | edit)
- Fanconi–Bickel syndrome (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Persistent hyperinsulinemia hypoglycemia of infancy (redirect page) (links | edit)
- 6-phosphogluconate dehydrogenase deficiency (links | edit)
- Transaldolase deficiency (links | edit)
- Danon disease (links | edit)
- Metabolic myopathy (links | edit)
- Enolase deficiency (links | edit)
- Iminoglycinuria (links | edit)
- Hydroxyacyl-Coenzyme A dehydrogenase (links | edit)
- MODY 2 (links | edit)
- Transient neonatal diabetes (links | edit)