Browse CGVdb Content: Total 90 Phenotypes Online
Click the Phenotype to browse |
| 1. |
ACE polymorphism
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| 2. |
Adrenal hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency
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| 3. |
Alcoholism
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| 4. |
ALDH2 polymorphism
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| 5. |
alpha-thalassemia 2
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| 6. |
Amyloidosis, Type I
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| 7. |
Androgen insensitivity syndrome
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| 8. |
Apert syndrome
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| 9. |
Astrocytoma
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| 10. |
Autoimmune thyroid disease
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| 11. |
Benzene poisoning
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| 12. |
Beta-Thalassaemia intermedia
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| 13. |
Beta-Thalassemia
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| 14. |
Bipolar affective disorder
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| 15. |
cancer susceptibility, chemotherapeutic response
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| 16. |
Colon cancer, Familial Nonpolyposis, Type 2
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| 17. |
Coronary artery disease
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| 18. |
Coronary heart disease
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| 19. |
CYP2E polymorphism
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| 20. |
DBH polymorphism
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| 21. |
Deafness, Sensorineural, Autosomal-Mitochondrial Type
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| 22. |
Defective apolipoprotein B-100
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| 23. |
Diabetes mellitus, Insulin-dependent
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| 24. |
Diabetes mellitus, noninsulin-dependent
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| 25. |
Epidermolysis bullosa pruriginosa
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| 26. |
Fabry disease
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| 27. |
Female infertility
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| 28. |
Fragile X syndrome
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| 29. |
Gaucher disease, Type 1
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| 30. |
Glucose-6-phosphate dehydrogenase deficiency
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| 31. |
Glycogen storage disease 1a
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| 32. |
Glycogen storage disease II
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| 33. |
Graves disease
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| 34. |
Hb H hydrops fetalis
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| 35. |
HBB polymorphism
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| 36. |
Hemochromatosis
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| 37. |
Hemoglobin D (Punjab)
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| 38. |
Hemoglobin H disease
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| 39. |
Hemoglobin J (Tashikuergan)
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| 40. |
Hemophilia A
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| 41. |
Hemophilia B
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| 42. |
Hepatic fibrosis, Severe, Susceptibility to, due to Schistosoma Mansoni infection
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| 43. |
Hyperbilirubinemia, Transient Familial Neonatal
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| 44. |
Hypercholesterolemia, Familial
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| 45. |
Hypergonadotropic ovarian failure, Hereditary
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| 46. |
Hyperlipidemia
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| 47. |
Hyperphenylalaninemia due to PTS deficiency
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| 48. |
Hypertension, Essential
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| 49. |
IDUA activity
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| 50. |
IDUA polymorphism
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| 51. |
Infertile male Syndrome
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| 52. |
Insulin resistance
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| 53. |
Leber hereditary optic neuropathy
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| 54. |
Leigh syndrome
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| 55. |
LHB polymorphism
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| 56. |
LPL polymorphism
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| 57. |
Lung cancer
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| 58. |
Male infertility
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| 59. |
Medullary thyroid carcinoma, Familial
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| 60. |
Methemoglobinemia, Type I
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| 61. |
Mitochondrial diseases
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| 62. |
Mitochondrial myopathy with predominant respiratory dysfunction
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| 63. |
mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
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| 64. |
MTHFR Heterogeneity
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| 65. |
Mucopolysaccharidosis type I
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| 66. |
Multiple endocrine neoplasia, Type II
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| 67. |
Muscular dystrophy, Limb-girdle, Type 2D
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| 68. |
Myocardial infarction
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| 69. |
Myoclonic epilepsy associated with ragged-red fibers
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| 70. |
Neurofibromatosis, Type II
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| 71. |
NQO1 polymorphism
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| 72. |
para-Bombay phenotype
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| 73. |
Parkinson disease
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| 74. |
Paroxysmal nocturnal haemoglobinuria
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| 75. |
Pfeiffer syndrome
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| 76. |
Phenylketonuria
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| 77. |
plasma lipid concentrations
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| 78. |
Plasma lipoprotein metabolism
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| 79. |
Preeclampsia/Eclampsia 1
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| 80. |
Progressive external ophthalmoplegia with mitochondrial DNA deletions
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| 81. |
Protein C deficiency, Type I
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| 82. |
Retinoblastoma, Incomplete Penetrance-Type
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| 83. |
Rett syndrome
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| 84. |
S-mephenytoin phenotype
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| 85. |
Schizophrenia
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| 86. |
Streptomycin ototoxicity
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| 87. |
Venous thromboembolism
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| 88. |
von Willebrand disease, Recessive form
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| 89. |
von Willebrand disease, type 2N
|
| 90. |
Wilson disease
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