Skip navigation
A service of the
U.S. National Library of Medicine
National Institutes of Health
Home
About MedlinePlus
Site Map
FAQs
Contact Us
Search MedlinePlus
Health Topics
Drugs & Supplements
Videos & Cool Tools
ESPAÑOL
To use the sharing features on this page, please enable JavaScript.
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
Neural Tube Defects
Ataxia see
Friedreich's Ataxia
Ataxia Telangiectasia
Birth Defects
Blood Coagulation Disorders see
Hemophilia
Brain Disorders, Inborn Genetic see
Genetic Brain Disorders
Brain Malformations
Canavan Disease see
Leukodystrophies
Cephalic Disorders see
Brain Malformations
Cerebral Palsy
Charcot-Marie-Tooth Disease
Chorionic Villi Sampling see
Prenatal Testing
Cleft Lip and Palate
Cleft Spine see
Spina Bifida
Cloning
Color Blindness
Congenital Heart Defects
Copper Storage Disease see
Wilson Disease
Craniofacial Abnormalities
Craniosynostosis see
Brain Malformations
;
Craniofacial Abnormalities
Cystic Fibrosis
Dandy-Walker Syndrome see
Brain Malformations
Down Syndrome
Duchenne Muscular Dystrophy see
Muscular Dystrophy
Dwarfism
Ehlers-Danlos Syndrome
Family History
FAS see
Fetal Alcohol Spectrum Disorders
Fetal Alcohol Spectrum Disorders
Fetal Alcohol Syndrome see
Fetal Alcohol Spectrum Disorders
Fetal Ultrasound see
Prenatal Testing
Fragile X Syndrome
FRAXA see
Fragile X Syndrome
Friedreich's Ataxia
Gaucher's Disease
Genes and Gene Therapy
Genetic Brain Disorders
Genetic Counseling
Genetic Disorders
Genetic Testing
Heart Defects see
Congenital Heart Defects
Heart Diseases, Congenital see
Congenital Heart Defects
Heart Murmur see
Congenital Heart Defects
Hemochromatosis
Hemoglobin SS Disease see
Sickle Cell Anemia
Hemophilia
Hepatolenticular Degeneration see
Wilson Disease
Human Genome Project see
Genes and Gene Therapy
Huntington's Disease
Hydrocephalus
Hypermobility Syndrome see
Ehlers-Danlos Syndrome
Iron Overload Disease see
Hemochromatosis
Klinefelter's Syndrome
Leukodystrophies
Maple Syrup Urine Disease see
Genetic Brain Disorders
Marfan Syndrome
Medicines and Pregnancy see
Pregnancy and Medicines
Metabolic Disorders
Mucolipidoses see
Metabolic Disorders
Mucopolysaccharidoses see
Metabolic Disorders
Muscular Dystrophy
Myelomeningocele see
Spina Bifida
Neural Tube Defects
Neurofibromatosis
Newborn Screening
Niemann-Pick Disease see
Genetic Brain Disorders
Open Spine see
Spina Bifida
Osteogenesis Imperfecta
Paternity Testing see
Genetic Testing
Phenylketonuria
PKU see
Phenylketonuria
Positional Plagiocephaly see
Craniofacial Abnormalities
Prader-Willi Syndrome
Pregnancy and Medicines
Prenatal Testing
Progeria see
Genetic Disorders
Rare Diseases
Rett Syndrome
Screening, Newborn see
Newborn Screening
Sickle Cell Anemia
Sickle Cell Disease see
Sickle Cell Anemia
SMA see
Spinal Muscular Atrophy
Spina Bifida
Spinal Muscular Atrophy
Tay-Sachs Disease
Tourette Syndrome
Treacher-Collins Syndrome see
Craniofacial Abnormalities
Trisomy 21 see
Down Syndrome
TSC see
Tuberous Sclerosis
Tuberous Sclerosis
Turner Syndrome
Usher Syndrome
VHL see
Von Hippel-Lindau Disease
Von Hippel-Lindau Disease
von Recklinghausen's Disease see
Neurofibromatosis
Wilson Disease