Inherited Health - Know Your Genetics

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Select a disease or topic to get reliable information about how your family health history can impact disease risk, symptoms, diagnosis, treatment, screening and prevention.

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  1. Aarskog Syndrome
  2. Abetalipoproteinemia (Bassen-Kornzweig Syndrome)
  3. Aceruloplasminemia
  4. Achondrogenesis
  5. Achondroplasia
  6. Acid Lipase Deficiency (Wolman Disease)
  7. Adenosine Deaminase Deficiency (ADA Deficiency)
  8. Adenosine Monophosphate Deaminase Deficiency
  9. Adoption
  10. Adrenal Cancer
  11. Age-Related Macular Degeneration (Macular Degeneration)
  12. Alagille Syndrome
  13. Albinism (Oculocutaneous Albinism)
  14. Alcohol (Caffeine and Alcohol Metabolism)
  15. Alcohol Flush Reaction
  16. Alexander Disease
  17. Alkaptonuria
  18. Allan-Herndon-Dudley Syndrome
  19. Alopecia (Hair Loss/Baldness)
  20. Alpha-1 Antitrypsin Deficiency (Alpha-1)
  21. Alpha-Mannosidosis
  22. Alpha-Thalassemia
  23. Alport Syndrome
  24. Alström Syndrome
  25. Alzheimer's Disease
  26. Amelogenesis Imperfecta
  27. Amish Lethal Microcephaly
  28. Amniotic Band Syndrome
  29. Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
  30. Ancestry Testing
  31. Andermann syndrome
  32. Andersen-Tawil Syndrome
  33. Androgen Insensitivity Syndrome
  34. Aneurysm
  35. Angelman Syndrome
  36. Aniridia
  37. Ankylosing Spondylitis
  38. Arakawa Syndrome 1 (Glutamate Formiminotransferase Deficiency)
  39. Arginase Deficiency
  40. Argininosuccinic Aciduria
  41. Aromatic l-Amino Acid Decarboxylase Deficiency (AADC Deficiency)
  42. Ashkenazi Jewish Diseases
  43. Aspartylglucosaminuria
  44. Asphyxiating Thoracic Dystrophy
  45. Asthma
  46. Ataxia with Oculomotor Apraxia
  47. Ataxia with Vitamin E Deficiency (AVED)
  48. Ataxia-Telangiectasia
  49. Atelosteogenesis Type 2
  50. Atrial Fibrillation
  51. Autism Spectrum Disorders (Autism)
  52. Autoimmune Conditions
  53. Autoimmune Polyglandular Syndrome Type 1 (APS Type 1)
  54. Autoimmune Thyroid Disorders (Graves' Disease/Hashimoto's Thyroiditis)
  55. Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE)
  56. Autosomal Dominant Partial Epilepsy with Auditory Features (ADPEAF)
  57. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)

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The role of genetics and family health history in the evaluation of disease risks is constantly evolving. Inherited Health does not collect and/or analyze all information relevant to the assessment of disease risk, such as the results of clinical tests, or perform complex risk calculations. As such, any tools or other content or information on this website, including risk statistics, are subject to change, are for informational purposes only, and are not a substitute for professional medical advice, diagnosis or treatment. You should always seek the advice of a physician regarding any questions you have about your family health history or specific medical conditions.More info

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