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Showing below up to 50 results in range #14,751 to #14,800.

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  1. HIV-modified psoriasis (Q98059)
  2. Hypoparathyroidism by glial cells missing B mutations (Q98058)
  3. Paget disease of bone in neoplastic disease, tarsus (Q98057)
  4. High basal metabolic rate (Q98056)
  5. Drug-exacerbated psoriasis (Q98055)
  6. Asphyxiation by drowning (Q98054)
  7. Paget disease of bone in neoplastic disease, metatarsus (Q98053)
  8. Dilated cardiomyopathy due to systemic sclerosis (Q98052)
  9. Paget disease of bone in neoplastic disease, ulna (Q98051)
  10. Paget disease of bone in neoplastic disease, clavicle (Q98050)
  11. Paget disease of bone in neoplastic disease, metacarpus (Q98049)
  12. Paget disease of bone in neoplastic disease, tibia (Q98048)
  13. Paget disease of bone in neoplastic disease, fibula (Q98047)
  14. B variant of hexosaminidase A deficiency (Q98046)
  15. Paget disease of bone in neoplastic disease, humerus (Q98045)
  16. Leber 'plus' disease (Q98044)
  17. Paget disease of bone in neoplastic disease, carpus (Q98043)
  18. Paget disease of bone in neoplastic disease, fingers (Q98042)
  19. Paget disease of bone in neoplastic disease, femur (Q98041)
  20. B1 variant of hexosaminidase A deficiency (Q98040)
  21. Paget disease of bone in neoplastic disease, pelvis (Q98039)
  22. Late infantile CACH syndrome (Q98038)
  23. Hexosaminidase activator deficiency (Q98037)
  24. Paget disease of bone in neoplastic disease, radius (Q98036)
  25. Paget disease of bone in neoplastic disease, scapula (Q98035)
  26. Iododerma (Q98034)
  27. Megaloencephalic leukoencephalopathy with subcortical cysts (Q98033)
  28. Cluster of differentiation 81 deficiency (Q98032)
  29. B-cell activating factor receptor deficiency (Q98031)
  30. Polycystic lipomembranous osteodysplasia - sclerosing leukoencephalopathy (Q98030)
  31. Internal chondromatosis (Q98029)
  32. Inducible costimulator deficiency (Q98028)
  33. Progressive cavitating leukoencephalopathy (Q98027)
  34. Transmembrane activator and calcium-modulating cyclophilin ligand interactor deficiency (Q98026)
  35. Jacobsen syndrome (Q98025)
  36. Leukoencephalopathy with bilateral anterior temporal lobe cysts (Q98024)
  37. Alagille syndrome type 1 (Q98023)
  38. Hypomyelination with atrophy of basal ganglia or cerebellum (Q98022)
  39. Juvenile or adult CACH syndrome (Q98021)
  40. Alagille syndrome type 2 (Q98020)
  41. Mitral valve insufficiency due to acute myocardial infarction with papillary muscle or chordal rupture (Q98019)
  42. Folliculitis keloidalis nuchae (Q98018)
  43. Bromoderma (Q98017)
  44. Cluster of differentiation 19 deficiency (Q98016)
  45. Cluster of differentiation 20 deficiency (Q98015)
  46. Osteochondromatosis syndrome (Q98014)
  47. Congenital or early infantile CACH syndrome (Q98013)
  48. Dyschondroplasia (Q98012)
  49. Acute salpingo-oophoritis following ectopic or molar pregnancy (Q98011)
  50. Acute eroded pyloric ulcer (Q98010)

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