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Genetic Conditions
Learn about genetic conditions

Genes determine what you inherit from your parents, from blood type and hair color to certain diseases. Changes in genes or chromosomes may cause health problems. We have hundreds of topics to answer your questions about genetic conditions. Maybe you're wondering about your baby's risk for disease or how to care for a child who has a genetic condition. Perhaps you're concerned about your own risk for a specific health problem. We can help.
Get the information you need in topics such as:
- Acquired von Willebrand Disease
- Alopecia Areata: Psoralen With Ultraviolet A Light (PUVA) Therapy
- Alpha-1 Antitrypsin Deficiency Genetic Testing
- Anesthesia: Malignant Hyperthermia Response
- Apolipoprotein E-4 Genetic (DNA) Test
- Ashkenazi Jewish Genetic Panel (AJGP)
- At-Home Genetic Tests
- Autosomal Recessive Conditions
- Birth Defects Testing
- Blood Transfusions for Sickle Cell Disease
- Blood-Clotting Disorders
- Cataracts in Children
- Clotting Factor Replacement for Hemophilia
- Colon Cancer Genetic Testing
- Color Blindness
- Complications From Klinefelter Syndrome
- Complications of Hemophilia
- Congenital Heart Defects
- Congenital Heart Defects: Pregnancy
- Congenital Heart Defects: Prostaglandins and Prostaglandin Inhibitors
- COPD and Alpha-1 Antitrypsin (AAT) Deficiency
- Coronary Artery Disease: Family History
- Cystic Fibrosis
- Cystic Fibrosis and Exercise
- Cystic Fibrosis Carrier Screening
- Cystic Fibrosis: Getting Enough Calories and Nutrients
- Cystic Fibrosis: Ways to Clear the Airways
- Down Syndrome
- Down Syndrome, Ages 1 Month to 1 Year
- Down Syndrome, Ages 1 to 5
- Down Syndrome, Ages 13 to 21
- Down Syndrome, Ages 5 to 13
- Down Syndrome, Ages Birth to 1 Month
- Down Syndrome: Grooming and Hygiene
- Down Syndrome: Helping Your Child Avoid Social Problems
- Down Syndrome: Helping Your Child Dress Independently
- Down Syndrome: Helping Your Child Eat Independently
- Down Syndrome: Helping Your Child Learn to Communicate
- Down Syndrome: Helping Your Child Learn to Walk and Use Other Motor Skills
- Down Syndrome: Training and Therapy for Young People
- Dupuytren's Disease: Surgery Complications
- Familial Lipid Disorders
- Family History and the Risk for Breast or Ovarian Cancer
- Family History of Epilepsy
- First-Trimester Screening for Birth Defects
- Genetic Test for Clopidogrel
- Genetic Testing: Ethical, Legal, and Religious Issues
- Genetics
- Hair Loss
- Hemochromatosis
- Hemochromatosis Genetic Screening
- Hemophilia
- Hemophilia: Preventing Bleeding Episodes
- Hemophilia: Treatment for People Who Have Inhibitors
- Hemophilia: Understanding Genetic Risk
- Hirschsprung's Disease
- Homocystinuria
- How Cystic Fibrosis Affects Breathing and the Lungs
- How Cystic Fibrosis Affects Digestion and the Pancreas
- How Cystic Fibrosis Affects the Bones
- How Cystic Fibrosis Affects the Reproductive System
- How Cystic Fibrosis Affects the Sweat Glands
- Huntington Disease Genetic Test
- Hyperthyroidism
- Hypertrophic Cardiomyopathy
- Hypertrophic Cardiomyopathy Types
- Independent Living for People With Disabilities
- Klinefelter Syndrome
- Lung Transplant for Cystic Fibrosis
- Multiple Pregnancy: Genetic Disorders and Birth Defects
- Nasal Potential Difference Test for Cystic Fibrosis
- Needle Aponeurotomy for Dupuytren's Disease
- Pain Management
- Phenylketonuria (PKU)
- PKU Diet
- Polycystic Ovary Syndrome (PCOS)
- Reducing Cancer Risk When You Are BRCA-Positive
- Replacement Therapy for Von Willebrand's Disease
- Sickle Cell Crisis
- Sickle Cell Disease
- Sickle Cell Disease: Acute Chest Syndrome
- Sickle Cell Disease: Aplastic Crisis
- Sickle Cell Disease: Dactylitis (Hand-Foot Syndrome)
- Sickle Cell Disease: Home Treatment for Priapism
- Sickle Cell Disease: Pain Management
- Sickle Cell Disease: Preventing Problems and Staying Healthy
- Sickle Cell Disease: Splenic Sequestration
- Sickle Cell Disease: Vision Problems
- Sickle Cell Disorders
- Sickle Cell Trait
- Stem Cell Transplant for Sickle Cell Disease
- Tay-Sachs Disease
- Thalassemia
- Tongue-Tie
- Tourette's Disorder
- Triple or Quad Screening for Birth Defects
- Types of Hair Loss
- Unwanted Hair in Women
- Von Willebrand's Disease
- Wolff-Parkinson-White Syndrome
- Alpha-Fetoprotein (AFP) in Blood
- Amniocentesis
- Autoimmune Disease Tests
- Breast Cancer (BRCA) Gene Test
- Cell-Free Fetal DNA Test
- Chorionic Villus Sampling (CVS)
- DNA Fingerprinting
- Galactosemia Test
- Genetic Test
- Hemochromatosis Gene Test (HFE Test)
- Hormone Inhibin A
- Human Chorionic Gonadotropin (HCG)
- Karyotype Test
- Nuchal Translucency Screening Test
- Phenylketonuria (PKU) Test
- Sickle Cell Test
- Sweat Test
- Tay-Sachs Enzyme Test
Current as of: October 9, 2017
Author: Healthwise Staff
Medical Review: Adam Husney, MD - Family Medicine & Martin J. Gabica, MD - Family Medicine