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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
NINDS Farber’s Disease Information Page
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
Genetics/Birth Defects
Food, Nutrition and Metabolism
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Clinical Trials Information
The NIH funds research studies that you may be able to join. Visit
clinicaltrials.gov
for a list of ongoing clinical trials.
This page was last reviewed on Thursday, July 02, 2009.