|
congenital stationary night blindness 1A
|
0010690 |
|
|
congenital stationary night blindness 1A X-linked
|
0010690 |
|
|
congenital stationary night blindness caused by mutation in NYX
|
0010690 |
|
|
congenital stationary night blindness type 1A
|
0010690 |
|
|
congenital stationary night blindness with myopia
|
0010690 |
|
|
night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive
|
0010690 |
|
|
night blindness, congenital stationary, type 1A
|
0010690 |
|
|
NYX congenital stationary night blindness
|
0010690 |
|
|
NYX-related congenital stationary night blindness
|
0010690 |
|
