|
1
|
(HPO:0000482)
|
Microcornea |
rare [HPO:skoehler]
|
|
|
|
102 / 7739
|
|
2
|
(HPO:0000613)
|
Photophobia |
rare [HPO:skoehler]
|
|
|
|
158 / 7739
|
|
3
|
(HPO:0000639)
|
Nystagmus |
|
|
|
|
555 / 7739
|
|
4
|
(HPO:0000646)
|
Amblyopia |
|
|
|
|
42 / 7739
|
|
5
|
(HPO:0008024)
|
Congenital nuclear cataract |
|
|
|
|
5 / 7739
|
|
6
|
(OMIM)
|
Cataract, congenital, multiple types |
|
|
|
|
2 / 7739
|
|
7
|
(OMIM)
|
Cataract, Coppock-like |
|
|
|
|
2 / 7739
|
|
8
|
(OMIM)
|
Cataract, zonular pulverulent |
|
|
|
|
3 / 7739
|
|
9
|
(HPO:0100018)
|
Nuclear cataract |
|
|
|
|
14 / 7739
|
|
10
|
(OMIM)
|
Opacities in embryonic, fetal, and infantile nuclei |
|
|
|
|
1 / 7739
|
|
11
|
(HPO:0000505)
|
Visual impairment |
|
|
|
|
297 / 7739
|
|
12
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|