|
1
|
(HPO:0000510)
|
Rod-cone dystrophy |
|
|
|
|
266 / 7739
|
|
2
|
(HPO:0000512)
|
Abnormal electroretinogram |
|
|
|
|
61 / 7739
|
|
3
|
(HPO:0000518)
|
Cataract |
|
|
|
|
454 / 7739
|
|
4
|
(HPO:0000580)
|
Pigmentary retinopathy |
|
|
|
|
49 / 7739
|
|
5
|
(HPO:0000662)
|
Nyctalopia |
|
|
|
|
92 / 7739
|
|
6
|
(HPO:0001123)
|
Visual field defect |
|
|
|
|
30 / 7739
|
|
7
|
(OMIM)
|
Abnormal electroretinograms in heterozygotes |
|
|
|
|
1 / 7739
|
|
8
|
(OMIM)
|
Inferior and inferonasal retinal pigmentation (e.g. 180380.0004 and 180380.0025) |
|
|
|
|
1 / 7739
|
|
9
|
(OMIM)
|
Superior hemisphere field impairment (e.g. 180380.0004 and 180380.0025) |
|
|
|
|
1 / 7739
|
|
10
|
(OMIM)
|
Early onset night blindness and abnormal fundus (e.g. 180380.0013) |
|
|
|
|
1 / 7739
|
|
11
|
(HPO:0010697)
|
Anterior pyramidal cataract |
|
|
|
|
22 / 7739
|
|
12
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
13
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|