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3. Alkalosis

4. Atrial Fibrillation

5. Pancreas Annulare

6. Pulmonary Valve Incompetence

7. Precocious Puberty

8. Protein S Deficiency

9. Arrythmogenic Right Ventricular Dysplasia

10. Proliferative Diabetic Retinopathy

11. Aortic Stenosis

12. Purine Nucleoside Phosphorylase Deficiency

13. Progressive Myoclonus Epilepsy of Unverricht-Lundborg Type

14. Autoimmune Hemolytic Anemia

15. Pseudohypoaldosteronism, Autosomal Recessive

16. Pendred Syndrome

17. Arteritis Temporalis

18. Acute Confusional State

19. Protoporphyria, Erythropoietic

20. APC Resistance

21. Premature Complexes, Atrial and Ventricular

22. PHT

23. Autosomal Dominant GTP Cyclohydrolase I [adGTPCH] Deficiency

24. Porphyria, Variegate

25. Paroxysmal Cold Hemoglobinuria

26. Polychondritis Recidivans

27. Acro-renal-ocular Syndrome

28. Pierre Robin Syndrome

29. Atrophic Polychondritis

30. Alcoholic Fatty Liver

31. Adrenocorticotropic Pituitary Insufficiency

32. Acute Liver Dystrophy

33. Preauricular Cyst

34. Phrenic Nerve Palsy

35. Amaurosis, Leber Congenital

36. Autosomal Dominant Mandibulofacial Dysostosis

37. Pancreatitis, Hereditary

38. Arrhythmogenic Right Ventricular Cardiomyopathy

39. Arndt-Gottron Scleromyxedema

40. Acanthosis Nigricans

41. Altered Levels of Coagulation Factors and Arterial Thrombosis

42. Palmitoylcarnitine Transferase

43. Acute Inflammation of the Oral Cavity

44. PFK Deficiency

45. Arthritis, Infectious

46. 5p Monosomy

47. Acid Cholesterol Ester Hydrolase Deficiency

48. Partial Tetrasomy 15(pter-q13)

49. Adult T-Cell Leukemia/Lymphoma

50. Primary Empty Sella