Metabolic Disorders Links:
Anatomy/Physiology Genes and Disease: Nutritional and Metabolic Disea - National Center for Biotechnology Information
ChildrenUnderstanding MPS and ML: Is Your Child Having an - National MPS Society
Clinical TrialsClinicalTrials.gov: Progeria - National Institutes of Health
ClinicalTrials.gov: Metabolic Diseases - National Institutes of Health
ClinicalTrials.gov: Mucolipidoses - National Institutes of Health
ClinicalTrials.gov: Mucopolysaccharidoses - National Institutes of Health
Diagnosis/SymptomsDiagnostic Testing: Hutchinson-Gilford Progeria S - Progeria Research Foundation, Inc.
DirectoriesOrganizations for Endocrine and Metabolic Disease - National Institute of Diabetes and Digestive and Kidney Diseases
Laboratory Directory-GeneReviews - Children's Health Care System, Seattle
Genetic and Rare Diseases Information Center - Office of Rare Diseases
US Clinic Directory Search - Children's Health Care System, Seattle
Disease ManagementManagement of MPS (Mucopolysaccharidosis) and ML ( - National MPS Society
Important Information for You and Your Doctors abo - Progeria Research Foundation, Inc.
GeneticsGenetics Home Reference: Mitochondrial trifunction - National Library of Medicine
Genetics Home Reference: Propionic acidemia - National Library of Medicine
Genetics Home Reference: Galactosemia - National Library of Medicine
Genetics Home Reference: Long-chain 3-hydroxyacyl- - National Library of Medicine
Genetics Home Reference: Methylmalonic acidemia - National Library of Medicine
Genetics Home Reference: Medium-chain acyl-coenzym - National Library of Medicine
Genetics Home Reference: Maple syrup urine disease - National Library of Medicine
Genetics Home Reference: Isovaleric acidemia - National Library of Medicine
Genetics Home Reference: Hutchinson-Gilford proger - National Library of Medicine
Genetics Home Reference: Homocystinuria - National Library of Medicine
Genetics Home Reference: Glucose-6-phosphate dehyd - National Library of Medicine
Genetics Home Reference: Biotinidase deficiency - National Library of Medicine
Genetics Home Reference: Alkaptonuria - National Library of Medicine
Genetics Home Reference: Trimethylaminuria - National Library of Medicine
Genetics Home Reference: Very long-chain acyl-coen - National Library of Medicine
Researchers Identify Gene for Premature Aging Diso - National Human Genome Research Institute
Genetics Home Reference: Niemann-Pick disease - National Library of Medicine
Genetics Home Reference: Familial lipoprotein lipa - National Library of Medicine
Genetics Home Reference: Primary hyperoxaluria - National Library of Medicine
National Institutes of HealthLipid Storage Diseases - National Institute of Neurological Disorders and Stroke
NutritionNutritional Supplements in Hutchinson-Gilford Prog - Progeria Research Foundation, Inc.
OrganizationsBarth Syndrome Foundation -
Save Babies Through Screening Foundation -
United Mitochondrial Disease Foundation -
Progeria Research Foundation, Inc. -
Oxalosis and Hyperoxaluria Foundation -
National MPS Society (Mucopolysaccharidoses) - National MPS Society
National Institute of Diabetes and Digestive and K -
OverviewsHereditary Disorders of Metabolism - Merck & Co., Inc.
Prevention/ScreeningNewborn Screening Tests - March of Dimes Birth Defects Foundation
Layperson's Guide to Tandem Mass Spectrometry - Save Babies Through Screening Foundation
ResearchBirth Defects and Developmental Disabilities - National Institute of Child Health and Human Development
NCI Study Demonstrates That Cellular Defects in Pr - National Cancer Institute
SeniorsLow Blood Sodium in Older Adults (Hyponatremia) - Mayo Foundation for Medical Education and Research
Specific ConditionsAmino Acid Metabolism Disorders - Merck & Co., Inc.
Methylmalonic Aciduria (MMA) - Save Babies Through Screening Foundation
What Is Progeria? - Progeria Research Foundation, Inc.
Guide to Understanding Sanfilippo Syndrome: Mucopo - National MPS Society
Guide to Understanding Morquio Syndrome: Mucopolys - National MPS Society
Guide to Understanding Maroteaux-Lamy Syndrome: Mu - National MPS Society
Guide to Understanding I-Cell Disease and Pseudo-H - National MPS Society
Guide to Understanding Hurler, Hurler-Scheie and S - National MPS Society
Guide to Understanding Hunter Syndrome: Mucopolysa - National MPS Society
Genes and Disease: Glucose Galactose Malabsorption - National Center for Biotechnology Information
G6PD Deficiency (Glucose-6-Phosphate Dehydrogenase - Nemours Foundation
Carnitine Palitoyl Transferase Deficiency Type II - Save Babies Through Screening Foundation
Carbohydrate Metabolism Disorders - Merck & Co., Inc.
Biotinidase Deficiency - Save Babies Through Screening Foundation
Barth Syndrome - National Institute of Neurological Disorders and Stroke
Amyloidosis - Merck & Co., Inc.
Amyloidosis - Mayo Foundation for Medical Education and Research
About Barth Syndrome - Barth Syndrome Foundation
Guide to Understanding Sly Syndrome: Mucopolysacch - National MPS Society
Hypophosphatasia - Osteoporosis and Related Bone Diseases-National Resource Center
Learning about Progeria - National Human Genome Research Institute
What Is Hyperoxaluria and Oxalosis? - Oxalosis and Hyperoxaluria Foundation
What Is a Urea Cycle Disorder? - National Urea Cycle Disorders Foundation
Type I Glycogen Storage Disease - American Liver Foundation
Pyruvate Metabolism Disorders - Merck & Co., Inc.
Propionic Acidemia - Save Babies Through Screening Foundation
Pompe Disease - National Institute of Neurological Disorders and Stroke
Nonketotic Hyperglycinemia - Save Babies Through Screening Foundation
Multiple CoA Carboxylase Deficiency - Save Babies Through Screening Foundation
Mucopolysaccharidoses - National Institute of Neurological Disorders and Stroke
Mucolipidoses - National Institute of Neurological Disorders and Stroke
Mitochondrial Myopathies - Muscular Dystrophy Association
Metabolic Diseases of Muscle - Muscular Dystrophy Association
Lipid Metabolism Disorders - Merck & Co., Inc.
Lesch-Nyhan Syndrome - National Institute of Neurological Disorders and Stroke
Learning about Trimethylaminuria - National Human Genome Research Institute
TreatmentFDA Approves First Treatment for Genetic Metabolic - Food and Drug Administration
|
Home