1 Addison's disease (with brain sclerosis)
2. Adrenal leukodystrophy
3. Adrenal dysplasia
4. Hematopoietic leukemia (bruton type)
5. Hematopoietic leukemia (Swiss type)
6. Eyes are albino
7, albinism-deafness syndrome
8. Wescott-aldridge syndrome
9. Ahlport syndrome
10, enamel hypoplasia (low maturity type)
1 1, enamel hypoplasia (dysplasia)
12, hereditary hypochromic anemia
13, Fabry's disease of angiokeratosis
14, congenital cataract
15, cerebellar ataxia
16, cerebellar ataxia
17, diffuse brain sclerosis
18, Charco-Marie-Tus (CMT)
19, no choroidal diseases.
20, choroidal retinopathy
2 1, color blindness (green series) and
22. Gallbladder fibrosis and hemophilia are common diseases of the third generation IVF.
23, nephrogenic diabetes insipidus
24. Diabetes insipidus (neurohypophysis type)
25. Congenital dyskeratosis
26, ectodermal dysplasia (anhidrosis)
27. Ehrlich-Dane syndrome (type V)
28, facial reproductive hypoplasia (Aarskog syndrome)
29. Focal skin dysplasia (an advantage associated with the X chromosome, which may be fatal to men)
30. Glucose -6- phosphate dehydrogenase deficiency
3 1, glycogen storage (type 8)
32. Hypogonadism (xy female type)
33, chronic granulomatosis
34 years old, hemophilia A.
35 years old, hemophilia B.
36, hydrocephalus (midbrain aqueduct stenosis)
37, low phosphate bloody rickets
38, ichthyosis
39. Dyschromatosis (an advantage associated with the X chromosome, which may be fatal to men)
40. Kalman syndrome
4 1, keratosis spinosa
42. Lesch-Niehan syndrome (hypoxanthine guanine phosphoribosyltransferase deficiency)
43. Luo syndrome
44. Retinal macular dystrophy
45. Menkes syndrome
46. Mental retardation (type I) is very useful for screening congenital Tang, and the third-generation IVF can also detect many mental retardation.
47. Mental retardation (FRAXE type)
48. Mental retardation (MRXI type)
49, microphthalmia (and a variety of malformations) (Leng Ci syndrome)
50, mucopolysaccharide storage disease Ⅱ (Hunter syndrome)
5 1, muscular dystrophy (Becker type)
52, muscular dystrophy (Duchenne type)
53. Muscular dystrophy (Ehrlich-Deutschland type)
54. Myotubular myopathy
Congenital static night blindness
56. Norris (Pseudoglioma)
57. nystagmus (eye movement or twitching)
58, ornithine formyltransferase deficiency (hyperammonemia type I)
59. Mouth-face-toe syndrome (type I) (an advantage associated with the X chromosome, which may be fatal to men)
60, sensory deafness (and * * * ataxia and vision loss)
6 1, sensory deafness (DNFZ type)
62, phosphoglycerate kinase deficiency
63. Lack of phosphoribosyl pyrophosphate synthase
64. Reifenstein syndrome
65. Retinitis pigmentosa
67. Spastic paralysis
68. spinal muscular atrophy
69. Delayed spinal dysplasia
70. Testicular feminization syndrome
7 1, hereditary thrombocytopenia
72, thyroxine binding globulin deficiency or variation.
73, Xg blood group system
74. Thalassemia