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Showing below up to 50 results in range #23,651 to #23,700.

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  1. Beery-baby syndrome (Q89159)
  2. Hepatic methionine adenosyltransferase deficiency (Q89158)
  3. Hypermethioninaemia (Q89157)
  4. Brain demyelination due to methionine adenosyltransferase deficiency (Q89156)
  5. Cystathioninemia (Q89155)
  6. Methionine malabsorption syndrome (Q89154)
  7. Deficiency of cysteine desulfhydrase (Q89153)
  8. Other genetic defects of methionine cycle or sulfur amino acid metabolism (Q89152)
  9. Psychomotor retardation and myopathy due to S-adenosylhomocysteine hydrolase deficiency (Q89151)
  10. Cystathioninuria (Q89150)
  11. Homocystinuria without methylmalonic aciduria (Q89149)
  12. Postcaval ureter (Q89148)
  13. Ankylosing vertebral hyperostosis with tylosis (Q89147)
  14. Deficiency of cystathionase (Q89146)
  15. Ectopic ureter or ureteric orifice (Q89145)
  16. Cerebrofaciothoracic dysplasia (Q89144)
  17. Glycine N-methyltransferase deficiency (Q89143)
  18. Spondylocostal dysostosis, autosomal recessive (Q89142)
  19. Neoplastic microangiopathic haemolytic anaemia (Q89141)
  20. Syndromic progressive noninfectious anterior vertebral fusion (Q89140)
  21. Ischio-vertebral syndrome (Q89139)
  22. Dwarfism - tall vertebrae (Q89138)
  23. Frontonasal dysplasia - Klippel-Feil syndrome (Q89137)
  24. Cerebrocostomandibular syndrome (Q89136)
  25. Congenital deviation of ureter (Q89135)
  26. Melhem-Fahl syndrome (Q89134)
  27. Parakeratosis pustulosa (Q89133)
  28. Spondylocostal dysostosis, autosomal dominant (Q89132)
  29. Lumbar malsegmentation - short stature (Q89131)
  30. Plaque psoriasis with pustules (Q89130)
  31. Infantile pustular psoriasis (Q89129)
  32. Late infantile neuronal ceroid lipofuscinosis (Q89128)
  33. Cerebral lipidosis myoclonic variant (Q89127)
  34. Ankylosis of cervical spinal joint (Q89126)
  35. Long-term memory (Q89125)
  36. Adult neuronal ceroid lipofuscinosis (Q89124)
  37. Short-term memory (Q89123)
  38. Juvenile neuronal ceroid lipofuscinosis (Q89122)
  39. Cerebroretinal lipidosis (Q89121)
  40. Congenital neuronal ceroid lipofuscinosis (Q89120)
  41. Fall or jump of undetermined intent from playground equipment (Q89119)
  42. Retrieval and processing of memory (Q89118)
  43. Finnish variant of late infantile neuronal ceroid lipofuscinosis (Q89117)
  44. Hereditary dentine defects (Q89116)
  45. Ekman-Westborg-Julin syndrome (Q89115)
  46. Cerebral lipidoses (Q89114)
  47. Annular and circinate pustular psoriasis (Q89113)
  48. Selective X-linked tooth agenesis (Q89112)
  49. Neuronal ceroid lipofuscinosis type 10 (Q89111)
  50. Ankylosis of lumbar spinal joint (Q89110)

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