Health Information
Metabolic Disorders
NIDDK
National Institute of Diabetes and Digestive and Kidney Diseases
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
NIAMS
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Call (877) 22-NIAMS or (301) 495-4484 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
Related Topics
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 last reviewed on
Thursday, April 07, 2011
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