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Attention, chocolate lovers: You may not be able to help yourselves. Swiss and British scientists have linked the widespread love of chocolate to a chemical "signature" that may be programmed into our metabolic systems.
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Genetics/Birth Defects
- Abnormalities see Birth Defects
- Achondroplasia see Dwarfism
- Adrenoleukodystrophy see Leukodystrophies
- Alpha-1 Antitrypsin Deficiency
- Amniocentesis see Prenatal Testing
- Anencephaly see Neural Tube Defects
- Arnold-Chiari Malformation see Head and Brain Malformations
- Ataxia Telangiectasia
- Birth Defects
- Blood Coagulation Disorders see Bleeding Disorders
- Brain Disorders, Inborn Genetic see Genetic Brain Disorders
- Brain Malformations see Head and Brain Malformations
- Canavan Disease see Leukodystrophies
- Cerebral Palsy
- Charcot-Marie-Tooth Disease
- Chorionic Villi Sampling see Prenatal Testing
- Cleft Lip and Palate
- Cloning
- Congenital Heart Disease
- Cystic Fibrosis
- Dandy-Walker Syndrome see Head and Brain Malformations
- Down Syndrome
- Duchenne Muscular Dystrophy see Muscular Dystrophy
- Dwarfism
- Ehlers-Danlos Syndrome
- FRAXA see Fragile X Syndrome
- Family Medical History see Genetic Counseling
- Fetal Alcohol Syndrome
- Fetal Ultrasound see Prenatal Testing
- Fragile X Syndrome
- Gaucher's Disease
- Genes and Gene Therapy
- Genetic Brain Disorders
- Genetic Counseling
- Genetic Disorders
- Genetic Testing
- Head and Brain Malformations
- Heart Diseases, Congenital see Congenital Heart Disease
- Heart Murmur see Congenital Heart Disease
- Hemochromatosis
- Hemophilia
- Hepatolenticular Degeneration see Wilson's Disease
- Human Genome Project see Genes and Gene Therapy
- Huntington's Disease
- Hydrocephalus
- Hypermobility Syndrome see Ehlers-Danlos Syndrome
- Klinefelter's Syndrome
- Leukodystrophies
- Maple Syrup Urine Disease see Genetic Brain Disorders
- Marfan Syndrome
- Metabolic Disorders
- Mucolipidoses see Metabolic Disorders
- Mucopolysaccharidoses see Metabolic Disorders
- Muscular Dystrophy
- Neural Tube Defects
- Neurofibromatosis
- Newborn Screening
- Niemann-Pick Disease see Genetic Brain Disorders
- Osteogenesis Imperfecta
- PKU see Phenylketonuria
- Paternity Testing see Genetic Testing
- Phenylketonuria
- Prader-Willi Syndrome
- Prenatal Testing
- Progeria see Metabolic Disorders
- Rare Diseases
- Sickle Cell Anemia
- Spina Bifida
- Spinal Muscular Atrophy
- Tay-Sachs Disease
- Tourette Syndrome
- Tuberous Sclerosis
- Turner's Syndrome
- Wilson's Disease
- von Recklinghausen's Disease see Neurofibromatosis