Neurological disorders |
100 |
0.277 |
0.231–0.323 |
|
|
ID – all |
58 |
0.161 |
0.123–0.199 |
|
|
ID – mild |
27 |
0.075 |
0.048–0.102 |
F70 |
249500 |
ID – moderate |
18 |
0.050 |
0.027–0.072 |
F71 |
|
ID – severe or profound |
13 |
0.036 |
0.017–0.055 |
F72, F73 |
611091 |
Cerebral palsy |
16 |
0.044 |
0.023–0.066 |
G80.9 |
605388 |
Down syndrome |
11 |
0.030 |
0.013–0.048 |
Q90.9 |
190685 |
Epilepsy |
6 |
0.017 |
0.003–0.030 |
G40 |
607208 |
Neuropathy |
3 |
0.008 |
−0.001 to 0.018 |
G60 |
605253 |
Alzheimer disease |
1 |
0.003 |
−0.003 to 0.008 |
F00.1 |
104300 |
Microcephaly |
1 |
0.003 |
−0.003 to 0.008 |
Q02 |
251200 |
Multiple sclerosis |
1 |
0.003 |
−0.003 to 0.008 |
G35 |
126200 |
Spastic paraplegia |
1 |
0.003 |
−0.003 to 0.008 |
G82.1 |
182600 |
Spina bifida |
1 |
0.003 |
−0.003 to 0.008 |
Q05 |
182940 |
Tremor |
1 |
0.003 |
−0.003 to 0.008 |
G25.0 |
190300 |
Sensorineural defects |
70 |
0.194 |
0.153–0.235 |
|
|
Deaf–mute |
48 |
0.133 |
0.098–0.168 |
H90 |
304500 |
Mute only |
19 |
0.053 |
0.030–0.076 |
R47.0 |
|
Stuttering |
3 |
0.008 |
−0.001 to 0.018 |
F98.5 |
184450 |
Limb defects |
60 |
0.166 |
0.128–0.205 |
|
|
Talipes or clubfoot |
13 |
0.036 |
0.017–0.055 |
Q66.9 |
119800 |
Limb amputations |
12 |
0.033 |
0.015–0.052 |
Q73.8 |
217100 |
Polydactyly (poly.; all) |
8 |
0.022 |
0.007–0.037 |
|
|
Poly., preaxial type I |
4 |
0.011 |
0.000–0.022 |
Q69.1 |
174400 |
Poly., postaxial type A |
3 |
0.008 |
−0.001 to 0.018 |
Q69.0;Q69.2 |
174200 |
Poly., postaxial type B |
1 |
0.003 |
−0.003 to 0.008 |
Q69.0;Q69.2 |
174200 |
Syndactyly (synd.; all) |
8 |
0.022 |
0.007–0.037 |
|
|
Synd., type 1c |
3 |
0.008 |
−0.001 to 0.018 |
Q70.1 |
|
Synd., type 1a |
2 |
0.006 |
−0.002 to 0.013 |
Q70.3 |
609815 |
Synd., type II |
2 |
0.006 |
−0.002 to 0.013 |
Q70.4 |
186000 |
Synd., type 1d |
1 |
0.003 |
−0.003 to 0.008 |
Q70.2 |
|
Contractures |
5 |
0.014 |
0.002–0.026 |
M21.8 |
259450 |
Brachydactyly, 4th toe |
2 |
0.006 |
−0.002 to 0.013 |
Q72.8 |
113475 |
Oligodactyly |
2 |
0.006 |
−0.002 to 0.013 |
Q73.8 |
176240 |
Split-hand split-foot |
2 |
0.006 |
−0.002 to 0.013 |
Q72.7 |
183600 |
Brachy-mesophalangy |
1 |
0.003 |
−0.003 to 0.008 |
|
112800 |
Camptodactyly |
1 |
0.003 |
−0.003 to 0.008 |
Q68.1 |
114200 |
Clinodactyly |
1 |
0.003 |
−0.003 to 0.008 |
Q74.0 |
|
Constriction ring |
1 |
0.003 |
−0.003 to 0.008 |
Q79.8 |
217100 |
Leg length discrepancy |
1 |
0.003 |
−0.003 to 0.008 |
Q72.9 |
|
Overriding toe |
1 |
0.003 |
−0.003 to 0.008 |
|
|
Radial hemimelia |
1 |
0.003 |
−0.003 to 0.008 |
Q71.8 |
114500 |
Ulnar hemimelia |
1 |
0.003 |
−0.003 to 0.008 |
Q71.8 |
|
Eye or visual impairments |
55 |
0.152 |
0.115–0.189 |
|
|
Squint eye (esotropia) |
17 |
0.047 |
0.025–0.069 |
H50.0 |
185100 |
Squint eye (exotropia) |
7 |
0.019 |
0.005–0.034 |
H50.1 |
|
Blindness |
14 |
0.039 |
0.019–0.059 |
H54.0 |
|
High myopia |
13 |
0.036 |
0.017–0.055 |
H52.1 |
160700 |
Anophthalmia |
2 |
0.006 |
−0.002 to 0.013 |
Q11.1 |
|
Color blindness |
1 |
0.003 |
−0.003 to 0.008 |
H53.5 |
303800 |
Congenital nystagmus |
1 |
0.003 |
−0.003 to 0.008 |
H55 |
617297 |
Musculoskeletal defects |
37 |
0.102 |
0.071–0.134 |
|
|
Dwarfisms |
8 |
0.022 |
0.007–0.037 |
Q77.4 |
100800 |
Muscular atrophy |
7 |
0.019 |
0.005–0.034 |
G12.1 |
253300 |
Muscular dystrophy |
7 |
0.019 |
0.005–0.034 |
G71.0 |
310200 |
Kyphoscoliosis |
4 |
0.011 |
0.000–0.022 |
M41.9 |
610170 |
Congenital hip dislocation |
3 |
0.008 |
−0.001 to 0.018 |
Q65 |
142700 |
Kyphosis |
2 |
0.006 |
−0.002 to 0.013 |
Q76.4 |
|
Mucopolysaccharidosis |
1 |
0.003 |
−0.003 to 0.008 |
E76.3 |
607014 |
Pectus carinatum |
1 |
0.003 |
−0.003 to 0.008 |
Q67.7 |
245600 |
Pectus excavatum |
1 |
0.003 |
−0.003 to 0.008 |
Q67.6 |
600399 |
Rickets |
1 |
0.003 |
−0.003 to 0.008 |
E83.3 |
277440 |
Spinal muscular atrophy |
1 |
0.003 |
−0.003 to 0.008 |
G12.1 |
253300 |
Torticollis |
1 |
0.003 |
−0.003 to 0.008 |
M43.6 |
189600 |
Ectodermal anomalies |
13 |
0.036 |
0.017–0.055 |
|
|
Ectodermal dysplasia |
3 |
0.008 |
−0.001 to 0.018 |
Q82.4 |
224900 |
Anonychia |
2 |
0.006 |
−0.002 to 0.013 |
Q84.3 |
206800 |
Early tooth decay |
2 |
0.006 |
−0.002 to 0.013 |
K02 |
|
Ichthyosis |
2 |
0.006 |
−0.002 to 0.013 |
Q80.1 |
602400 |
Albinism |
1 |
0.003 |
−0.003 to 0.008 |
E70.3 |
300500 |
Dentinogenesis imperfecta |
1 |
0.003 |
−0.003 to 0.008 |
K00.5 |
125490 |
Eczema |
1 |
0.003 |
−0.003 to 0.008 |
L20 |
603165 |
Epidermolysis |
1 |
0.003 |
−0.003 to 0.008 |
Q81.2 |
226600 |
Blood disorders |
12 |
0.033 |
0.015–0.052 |
|
|
Thalassemia (major = 8; intermedia = 1) |
9 |
0.025 |
0.009–0.041 |
D56.1 |
613985 |
Hemophilia |
3 |
0.008 |
−0.001 to 0.018 |
D66 |
306700 |
Others |
14 |
0.039 |
0.019–0.059 |
|
|
Cleft palate |
4 |
0.011 |
0.000–0.022 |
Q35 |
119540 |
Heart septal defect |
3 |
0.008 |
−0.001 to 0.018 |
Q24.9 |
600001 |
Lymphedema |
2 |
0.006 |
−0.002 to 0.013 |
Q82.0 |
153100 |
Urogenital defect |
3 |
0.008 |
−0.001 to 0.018 |
Q62 |
617641 |
Cleft lip |
1 |
0.003 |
−0.003 to 0.008 |
Q36 |
119530 |
Enuresis |
1 |
0.003 |
−0.003 to 0.008 |
R32 |
600631 |
Total |
361 |
1.000 |
1.000–1.000 |
|
|