AccessDNA - Know Your Genetics

> Diseases & Topics
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.

Browse alphabetically by condition, test or topic:

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  1. Macular Degeneration (Age-Related Macular Degeneration)
  2. Malignant Hyperthermia
  3. Malonyl-Coenzyme A Decarboxylase Deficiency (MCD Deficiency)
  4. Manic Depression (Bipolar Disorder)
  5. Maple Syrup Urine Disease (MSUD)
  6. Marfan Syndrome
  7. Marinesco-Sjögren Syndrome
  8. McCune-Albright Syndrome
  9. McKusick-Kaufman Syndrome (MKS)
  10. McLeod Neuroacanthocytosis Syndrome (McLeod Syndrome)
  11. Medical Genetic Testing (Clinical Genetic Testing)
  12. Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (MCAD Deficiency)
  13. Megalencephalic Leukoencephalopathy with Subcortical Cysts (Van der Knaap Disease)
  14. Melnick-Needles Syndrome
  15. Menkes Syndrome (Menkes Disease)
  16. Mental Illness
  17. Mental Retardation/Developmental Delay
  18. Metachromatic Leukodystrophy
  19. Methylmalonic Acidemia
  20. Milroy Disease
  21. Miscarriages/Stillbirths (Recurrent Pregnancy Loss/Stillbirth)
  22. Mitochondrial Conditions
  23. Mitochondrial Encephalomyopathy, Lactic acidosis, and Stroke-like Episodes (MELAS)
  24. Mitochondrial Neurogastrointestinal Encephalopathy Disease (MNGIE Disease)
  25. Mitochondrial Trifunctional Protein Deficiency (MTP Deficiency)
  26. Modes of Inheritance (Patterns of Inheritance)
  27. Mohr-Tranebjærg syndrome (Deafness-Dystonia-Optic Neuronopathy Syndrome)
  28. Monosaccharide Malabsorption (Glucose-Galactose Malabsorption)
  29. Mowat-Wilson Syndrome
  30. Muckle-Wells Syndrome
  31. Mucolipidosis II Alpha/Beta (I-Cell Disease)
  32. Mucolipidosis III Alpha/Beta (Pseudo-Hurler Polydystrophy)
  33. Mucolipidosis III Gamma (Pseudo-Hurler Polydystrophy)
  34. Mucolipidosis Type IV
  35. Mucopolysaccharidosis Type I (MPS I)
  36. Mucopolysaccharidosis Type II (Hunter Syndrome)
  37. Muenke Syndrome
  38. Multiminicore Disease
  39. Multiple Endocrine Neoplasia (MEN)
  40. Multiple Epiphyseal Dysplasia
  41. Multiple Sclerosis (MS)
  42. Muscular Dystrophy (MD)
  43. Myostatin-Related Muscle Hypertrophy
  44. Myotonia Congenita
  45. Myotonic Dystrophy

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The role of genetics and family health history in the evaluation of disease risks is constantly evolving. AccessDNA 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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