|
1
|
(HPO:0000548)
|
Cone/cone-rod dystrophy |
|
|
|
|
47 / 7739
|
|
2
|
(HPO:0000618)
|
Blindness |
|
|
|
|
124 / 7739
|
|
3
|
(HPO:0000662)
|
Nyctalopia |
|
|
|
|
92 / 7739
|
|
4
|
(HPO:0001000)
|
Abnormality of skin pigmentation |
|
|
|
|
105 / 7739
|
|
5
|
(OMIM)
|
Night blindness followed by complete blindness |
|
|
|
|
1 / 7739
|
|
6
|
(OMIM)
|
Bone corpuscle-like pigmentation in equatorial and peripheral areas |
|
|
|
|
1 / 7739
|
|
7
|
(OMIM)
|
Attenuated blood vessels in periphery |
|
|
|
|
1 / 7739
|
|
8
|
(OMIM)
|
Macula clear in early stages |
|
|
|
|
1 / 7739
|
|
9
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
10
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
11
|
(HPO:0000510)
|
Rod-cone dystrophy |
|
|
|
|
266 / 7739
|