Overview

• Hereditary Disorders of Metabolism (Merck & Co., Inc.)
• Metabolic Disorders (WebMDHealth)

Specific Conditions From MedLine

• About Barth Syndrome (Barth Syndrome Foundation)
• About Primary Hyperoxaluria (Oxalosis and Hyperoxaluria Foundation)
• Amino Acid Metabolism Disorders (Merck & Co., Inc.)
• Amyloidosis (Mayo Foundation for Medical Education and Research)
• Amyloidosis (Merck & Co., Inc.)
• Barth Syndrome (National Institute of Neurological Disorders and Stroke)
• Biotinidase Deficiency (Save Babies Through Screening Foundation)
• Carbohydrate Metabolism Disorders (Merck & Co., Inc.)
• Carnitine Palitoyl Transferase Deficiency Type II (CPT-II) (Save Babies Through Screening Foundation)
• G6PD Deficiency (Glucose-6-Phosphate Dehydrogenase) (Nemours Foundation)
• Genes and Disease: Glucose Galactose Malabsorption (GGM) (National Center for Biotechnology Information)
• Guide to Understanding Hunter Syndrome: Mucopolysaccharidosis (MPS) II (National MPS Society)
• Guide to Understanding Hurler, Hurler-Scheie and Scheie Syndromes: Mucopolysaccharidosis (MPS) I (National MPS Society)
• Guide to Understanding I-Cell Disease and Pseudo-Hurler Polydystrophy: Mucolipidoses (ML) II and III (National MPS Society)
• Guide to Understanding Maroteaux-Lamy Syndrome: Mucopolysaccharidosis (MPS) VI (National MPS Society)
• Guide to Understanding Morquio Syndrome: Mucopolysaccharidosis (MPS) IV (National MPS Society)
• Guide to Understanding Sanfilippo Syndrome: Mucopolysaccharidosis (MPS) III (National MPS Society)
• Guide to Understanding Sly Syndrome: Mucopolysaccharidosis (MPS) VII (National MPS Society)
• Hypophosphatasia (Osteoporosis and Related Bone Diseases-National Resource Center)
• Learning about Progeria (National Human Genome Research Institute)
• Learning about Trimethylaminuria (National Human Genome Research Institute)
• Lesch-Nyhan Syndrome (National Institute of Neurological Disorders and Stroke) - Short Summary
• Lipid Metabolism Disorders (Merck & Co., Inc.)
• Metabolic Diseases of Muscle (Muscular Dystrophy Association)
• Methylmalonic Aciduria (MMA) (Save Babies Through Screening Foundation)
• Mitochondrial Myopathies (Muscular Dystrophy Association)
• Mucolipidoses (National Institute of Neurological Disorders and Stroke)
• Mucopolysaccharidoses (National Institute of Neurological Disorders and Stroke)
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• Multiple CoA Carboxylase Deficiency (Save Babies Through Screening Foundation)
• Nonketotic Hyperglycinemia (Save Babies Through Screening Foundation)
• Pompe Disease (National Institute of Neurological Disorders and Stroke)
• Propionic Acidemia (Save Babies Through Screening Foundation)
• Pyruvate Metabolism Disorders (Merck & Co., Inc.)
• Type I Glycogen Storage Disease (American Liver Foundation)
• What Is a Urea Cycle Disorder? (National Urea Cycle Disorders Foundation)
• What Is Progeria? (Progeria Research Foundation, Inc.)

Genetics From MedLine

• Genetics Home Reference: Alkaptonuria (National Library of Medicine)
• Genetics Home Reference: Biotinidase deficiency (National Library of Medicine)
• Genetics Home Reference: Familial lipoprotein lipase deficiency (National Library of Medicine)
• Genetics Home Reference: Galactosemia (National Library of Medicine)
• Genetics Home Reference: Homocystinuria (National Library of Medicine)
• Genetics Home Reference: Hutchinson-Gilford progeria syndrome (National Library of Medicine)
• Genetics Home Reference: Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (National Library of Medicine)
• Genetics Home Reference: Maple syrup urine disease (National Library of Medicine)
• Genetics Home Reference: Medium-chain acyl-coenzyme A dehydrogenase deficiency (National Library of Medicine)
• Genetics Home Reference: Methylmalonic acidemia (National Library of Medicine)
• Genetics Home Reference: Mitochondrial trifunctional protein deficiency (National Library of Medicine)
• Genetics Home Reference: Niemann-Pick disease (National Library of Medicine)
• Genetics Home Reference: Primary hyperoxaluria (National Library of Medicine)
• Genetics Home Reference: Propionic acidemia (National Library of Medicine)
• Genetics Home Reference: Very long-chain acyl-coenzyme A dehydrogenase deficiency (National Library of Medicine)
• Researchers Identify Gene for Premature Aging Disorder (Progeria) (National Human Genome Research Institute)

Ogranizations and Patient-Centered Sites

• Barth Syndrome Foundation
• National Institute of Diabetes and Digestive and Kidney Diseases
• National MPS Society (Mucopolysaccharidoses) (National MPS Society)
• Oxalosis and Hyperoxaluria Foundation
• Progeria Research Foundation, Inc.
• Save Babies Through Screening Foundation
• United Mitochondrial Disease Foundation