|
1
|
(HPO:0000519)
|
Congenital cataract |
rare [HPO:skoehler]
|
|
|
|
73 / 7739
|
|
2
|
(HPO:0000556)
|
Retinal dystrophy |
rare [HPO:skoehler]
|
|
|
|
65 / 7739
|
|
3
|
(HPO:0001135)
|
Chorioretinal dystrophy |
|
|
|
|
18 / 7739
|
|
4
|
(HPO:0007731)
|
Chorioretinal dysplasia |
|
|
|
|
16 / 7739
|
|
5
|
(HPO:0007973)
|
Retinal dysplasia |
|
|
|
|
27 / 7739
|
|
6
|
(HPO:0001115)
|
Posterior polar cataract |
|
|
|
|
8 / 7739
|
|
7
|
(HPO:0007971)
|
Lamellar cataract |
|
|
|
|
6 / 7739
|
|
8
|
(HPO:0100018)
|
Nuclear cataract |
|
|
|
|
14 / 7739
|
|
9
|
(OMIM)
|
Cataract, complete |
|
|
|
|
3 / 7739
|
|
10
|
(OMIM)
|
Cataract, juvenile-onset (in some patients) |
|
|
|
|
1 / 7739
|
|
11
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
12
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|