Genetic Disease Genetic DiseaseRelated Doctor's & Expert's Views « Back to Genetic Disease Index Sorted Alphabetically A-Z Sort by popularity Acquired Methemoglobinemia Angelina Jolie's Mastectomy Colon Cancer, The Genetic Factor Down Syndrome Causes and Symptoms Family Medical History Fumbled Genetic Testing: Families With Breast Cancer Kiss of Death Gets Nobel Prize Noonan Syndrome Diagnosis Sickle Trait and Sickle Cell Disease What Is Hyperdontia? Sorted by Popularity (as on MedicineNet) Sort alphabetically Down Syndrome Causes and Symptoms Noonan Syndrome Diagnosis Angelina Jolie's Mastectomy Genetic Testing: Families With Breast Cancer What Is Hyperdontia? Acquired Methemoglobinemia Sickle Trait and Sickle Cell Disease Colon Cancer, The Genetic Factor Family Medical History Fumbled Kiss of Death Gets Nobel Prize Suggested Reading on Genetic Disease by Our Doctors Related Diseases & Conditions 95 articles Anemia Anemia is the condition of having less than the normal number of red blood cells or less than the normal quantity of hemoglobin in the blood. The oxygen-carrying Diabetes (Type 1 and Type 2) Diabetes is a chronic condition characterized by high levels of sugar (glucose) in the blood. The two types of diabetes are referred to as type 1 (insulin Hemochromatosis (Iron Overload) Hereditary hemochromatosis (iron overload) is an inherited disorder in which there is excessive accumulation of iron in the body. Individuals may have Allergy (Allergies) An allergy refers to a misguided reaction by our immune system in response to bodily contact with certain foreign substances. When these allergens come Atopic Dermatitis Eczema is a general term for many types dermatitis (skin inflammation). Atopic dermatitis is the most common of the many types of eczema. Other types of Pernicious Anemia Pernicious anemia is a blood disorder in which the body does not make enough red blood cells due to a lack of vitamin B12 in the blood. Pernicious anemia Hydrocephalus Hydrocephalus is an abnormal buildup of cerebrospinal fluid (CSF) in the ventricles of the brain. The fluid is often under increased pressure and can compress Graves' Disease Graves' disease is an autoimmune disease that affects the thyroid. Some of the symptoms of Graves' disease include hand tremors, rapid heartbeat, trouble Miscarriage Miscarriage is the medical term for the spontaneous loss of pregnancy from conception to 20 weeks gestation. Risk factors for a woman having a miscarriage Parkinson's Disease Parkinson's disease is a slowly progressive neurologic disease characterized by a fixed inexpressive face, a tremor at rest, slowing of voluntary movements, Deep Vein Thrombosis (DVT) Deep vein thrombosis (DVT) is a blood clot in a vein located deep in the muscles of the legs, thighs, pelvis (lower torso), or arms. The most common symptoms Depression Depression is an illness that involves the body, mood, and thoughts and affects the way a person eats and sleeps, the way one feels about oneself, and Myasthenia Gravis Myasthenia gravis, a chronic autoimmune neuromuscular disease. Varying degrees of weakness of the voluntary muscles of the body are the main characteristics. Hay Fever Hay fever (allergic rhinitis) is an irritation of the nose caused by pollen and is associated with the following allergic symptoms: nasal congestion, runny Amyotrophic Lateral Sclerosis (ALS) Amyotrophic lateral sclerosis (ALS, Lou Gehrig's disease) is a neurological disease that progresses rapidly. The disease attacks the nerve cells responsible Macular Degeneration Age-related macular degeneration (AMD) is a disease that gradually destroys the central vision. In people over 60, AMD is a leading cause of vision loss. Connective Tissue Disease Connective tissue disease is when the body's connective tissues come under attack, possibly becoming injured by inflammation. Inherited connective tissue Ehlers-Danlos Syndrome Ehlers-Danlos syndromes are genetic disorders that include symptoms such as loose joints, tissue weakness, easy bruising, and skin that stretches easily. Sickle Cell Disease (Sickle Cell Anemia) Sickle cell anemia (sickle cell disease), a blood disease which shortens life expectancy, is cause by an inherited abnormal hemoglobin. Symptoms may include Cystic Fibrosis Cystic fibrosis is a disease of the mucus and sweat glands. Cystic fibrosis is an inherited disease. The outcome of the disease leaves the body malnourished, Bipolar Disorder Bipolar disorder (or manic depression) is a mental illness characterized by depression, mania, and severe mood swings. Treatment may incorporate mood stabilizer Cerebral Palsy Cerebral palsy (CP) is an abnormality of motor function and postural tone acquired at an early age (even before birth). Cerebral palsy is generally caused Huntington's Disease Huntington's disease is the result of degeneration of neurons in areas of the brain. Huntington's disease is an inherited disorder. Early symptoms include Diabetes Insipidus Diabetes insipidus is a condition in which the patient has frequent urination. Symptoms of diabetes insipidus include irritable, listless, fever, vomiting, Marfan Syndrome Marfan syndrome is hereditary condition affecting connective tissue. A person with Marfan syndrome may exhibit the following symptoms and characteristics: Autism Spectrum Disorder (In Children and Adults) Autism in children and adults is a developmental disorder, characterized by impaired development in communication, social interaction, and behavior. Autism Beta Thalassemia Beta Thalassemia is the most familiar type of thalassemia. Thalassemia is not just one disease but rather a complex series of genetic (inherited) disorders Polycystic Kidney Disease (PKD) Polycystic kidney disease (PKD) is characterized by numerous cysts in the kidneys. Polycystic kidney disease is a genetic disorder. There are two major Pheochromocytoma Pheochromocytoma is a tumor of the adrenal gland. Pheochromocytomas are quite rare and the vast majority of them are entirely benign. 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