The following pages link to Inborn errors of carbohydrate metabolism
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Kjer's optic neuropathy (links | edit)
- Hunter syndrome (links | edit)
- Fucosidosis (links | edit)
- MERRF syndrome (links | edit)
- Mucolipidosis type IV (links | edit)
- Pseudo-Hurler polydystrophy (links | edit)
- I-cell disease (links | edit)
- Maroteaux–Lamy syndrome (links | edit)
- Aspartylglucosaminuria (links | edit)
- Pyruvate carboxylase deficiency (links | edit)
- Hyperoxaluria (links | edit)
- Sucrose intolerance (links | edit)
- Neuropathy, ataxia, and retinitis pigmentosa (links | edit)
- Triosephosphate isomerase deficiency (links | edit)
- Myophosphorylase (links | edit)
- Mitochondrial neurogastrointestinal encephalopathy syndrome (links | edit)
- Galactokinase deficiency (links | edit)
- Aldolase A deficiency (links | edit)
- Glycogen storage disease type VI (links | edit)
- Diabetes and deafness (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)
- Second wind (links | edit)
- Scheie syndrome (links | edit)
- Pearson syndrome (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Chronic progressive external ophthalmoplegia (links | edit)
- Hurler–Scheie syndrome (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Primary hyperoxaluria (links | edit)
- Beta-mannosidosis (links | edit)
- Hexokinase deficiency (links | edit)
- Galactosemic cataract (links | edit)
- Glycogen storage disease type IX (links | edit)
- Galactosialidosis (links | edit)
- 6-phosphogluconate dehydrogenase deficiency (links | edit)
- Transaldolase deficiency (links | edit)
- Danon disease (links | edit)
- Schindler disease (links | edit)
- Metabolic myopathy (links | edit)
- Enolase deficiency (links | edit)
- Congenital hemolytic anemia (links | edit)
- Mitochondrial encephalomyopathy (links | edit)
- MODY 2 (links | edit)
- Hyaluronidase deficiency (links | edit)