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50 phene records found

[show instead gene records]
  1. OMIA 000017-9986 Adrenal hyperplasia, congenital in Oryctolagus cuniculus (rabbit) Gene: CYP11A1

  2. OMIA 001243-9986 Alkaptonuria in Oryctolagus cuniculus (rabbit)

  3. OMIA 000077-9986 Ataxia, generic in Oryctolagus cuniculus (rabbit)

  4. OMIA 000155-9986 C3 deficiency in Oryctolagus cuniculus (rabbit)

  5. OMIA 000156-9986 C8 deficiency in Oryctolagus cuniculus (rabbit)

  6. OMIA 000162-9986 Cardiomyopathy, dilated in Oryctolagus cuniculus (rabbit)

  7. OMIA 000189-9986 Chondrodystrophy in Oryctolagus cuniculus (rabbit)

  8. OMIA 000197-9986 Cleft palate in Oryctolagus cuniculus (rabbit)

  9. OMIA 000201-9986 Coat colour, agouti in Oryctolagus cuniculus (rabbit) Gene: ASIP

  10. OMIA 000202-9986 Coat colour, albinism in Oryctolagus cuniculus (rabbit) Gene: TYR

  11. OMIA 001249-9986 Coat colour, brown in Oryctolagus cuniculus (rabbit) Gene: TYRP1

  12. OMIA 000031-9986 Coat colour, dilute in Oryctolagus cuniculus (rabbit) Gene: MLPH

  13. OMIA 000209-9986 Coat colour, dominant white in Oryctolagus cuniculus (rabbit)

  14. OMIA 001199-9986 Coat colour, extension in Oryctolagus cuniculus (rabbit) Gene: MC1R

  15. OMIA 001168-9986 Coronal suture synostosis in Oryctolagus cuniculus (rabbit)

  16. OMIA 001224-9986 Craniosynostosis in Oryctolagus cuniculus (rabbit)

  17. OMIA 000249-9986 Cyclopia in Oryctolagus cuniculus (rabbit)

  18. OMIA 000279-9986 Diabetes mellitus in Oryctolagus cuniculus (rabbit)

  19. OMIA 000312-9986 Dysautonomia in Oryctolagus cuniculus (rabbit)

  20. OMIA 002157-9986 Ectodermal dysplasia-9 in Oryctolagus cuniculus (rabbit) Gene: HOXC13

  21. OMIA 000327-9986 Ehlers-Danlos syndrome in Oryctolagus cuniculus (rabbit)

  22. OMIA 000344-9986 Epilepsy in Oryctolagus cuniculus (rabbit)

  23. OMIA 001461-9986 Gangliosidosis, GM2, type I (B variant) in Oryctolagus cuniculus (rabbit)

  24. OMIA 000411-9986 Glaucoma, generic in Oryctolagus cuniculus (rabbit)

  25. OMIA 000459-9986 Hernia, diaphragmatic in Oryctolagus cuniculus (rabbit)

  26. OMIA 000473-9986 Hip dysplasia in Oryctolagus cuniculus (rabbit)

  27. OMIA 000487-9986 Hydrocephalus in Oryctolagus cuniculus (rabbit)

  28. OMIA 000493-9986 Hydrops foetalis in Oryctolagus cuniculus (rabbit)

  29. OMIA 000499-9986 Hypercholesterolaemia in Oryctolagus cuniculus (rabbit)

  30. OMIA 001160-9986 Hyperlipidaemia in Oryctolagus cuniculus (rabbit) Gene: LDLR

  31. OMIA 002063-9986 Hyperlipidaemia due to ApoE knockout in Oryctolagus cuniculus (rabbit)

  32. OMIA 000540-9986 Hypotrichosis in Oryctolagus cuniculus (rabbit)

  33. OMIA 000618-9986 Macrostomus in Oryctolagus cuniculus (rabbit)

  34. OMIA 000621-9986 Malignant hyperthermia in Oryctolagus cuniculus (rabbit)

  35. OMIA 000629-9986 Megacolon in Oryctolagus cuniculus (rabbit)

  36. OMIA 000715-9986 Neuroaxonal dystrophy, generic in Oryctolagus cuniculus (rabbit)

  37. OMIA 001258-9986 Obesity in Oryctolagus cuniculus (rabbit)

  38. OMIA 000753-9986 Osteodystrophy in Oryctolagus cuniculus (rabbit)

  39. OMIA 000755-9986 Osteopetrosis in Oryctolagus cuniculus (rabbit)

  40. OMIA 001230-9986 Ovotesticular DSD (Disorder of Sexual Development) in Oryctolagus cuniculus (rabbit)

  41. OMIA 000783-9986 Pelger-Huet anomaly in Oryctolagus cuniculus (rabbit)

  42. OMIA 000807-9986 Polycystic kidney disease in Oryctolagus cuniculus (rabbit)

  43. OMIA 001566-9986 Rex coat in Oryctolagus cuniculus (rabbit) Gene: LIPH

  44. OMIA 000933-9986 Spina bifida in Oryctolagus cuniculus (rabbit)

  45. OMIA 000944-9986 Spongiform encephalopathy in Oryctolagus cuniculus (rabbit)

  46. OMIA 002067-9986 Syndactyly, type Ia in Oryctolagus cuniculus (rabbit)

  47. OMIA 000965-9986 Syringomyelia in Oryctolagus cuniculus (rabbit)

  48. OMIA 000770-9986 Tremor, X-linked in Oryctolagus cuniculus (rabbit) Gene: PLP1

  49. OMIA 001041-9986 Ventricular septal defect in Oryctolagus cuniculus (rabbit)

  50. OMIA 001056-9986 Von Willebrand disease, generic in Oryctolagus cuniculus (rabbit)