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NIDDK
National Institute of Diabetes and Digestive and Kidney Diseases
Directory of Endocrine and Metabolic Diseases Organizations
NINDS
National Institute of Neurological Disorders and Stroke
Barth Syndrome
Fabry's Disease
Lesch-Nyhan Syndrome Information Page
Menkes Disease
Mitochondrial Myopathies
Mucolipidoses
Mucopolysaccharidoses
Niemann-Pick Disease Information Page
NINDS Acid Lipase Disease Information Page
NINDS Alphabetical List of Disorders
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NINDS Gangliosidoses Information Page
Pompe Disease
Sandhoff Disease
Call (800) 352-9424 for more information
NLM
National Library of Medicine
Carnitine-acylcarnitine translocase deficiency
Genetics Home Reference: 3-hydroxy-3-methylglutaryl-CoA lyase Deficiency
Genetics Home Reference: 3-methylglutaconic aciduria
Genetics Home Reference: Carnitine Palmitoyltransferase I Deficiency
Genetics Home Reference: Carnitine Palmitoyltransferase II Deficiency
Genetics Home Reference: Glutaric acidemia type 1
Genetics Home Reference: Malonyl-CoA decarboxylase deficiency
Metabolic Disorders: Genetics Home Reference
Related Topics
Celiac Disease
Gaucher's Disease
Hemochromatosis
Phenylketonuria
Porphyria
Wilson's Disease
Bones, Joints and Muscles
Food, Nutrition and Metabolism
Genetics/Birth Defects
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This page was last reviewed on 7/10/2009