|
night blindness, congenital stationary
|
C536122 |
|
|
night blindness, congenital stationary, complete, autosomal recessive
|
C536122 |
|
|
night blindness, congenital stationary, incomplete, autosomal recessive
|
C536122 |
|
|
night blindness, congenital stationary, type 1
|
C536122 |
|
|
night blindness, congenital stationary, type 1a
|
C536122 |
|
|
night blindness, congenital stationary, type 1b
|
C536122 |
|
|
night blindness, congenital stationary, type 2
|
C536122 |
|
|
night blindness, congenital stationary, type 2a
|
C536122 |
|
|
night blindness, congenital stationary, type 2b
|
C536122 |
|
|
night blindness, congenital stationary, with myopia
|
C536122 |
|
|
Cone-rod synaptic disorder, congenital nonprogressive
|
C536122 |
|
|
congenital stationary, incomplete, autosomal recessive night blindness
|
C536122 |
|
|
congenital stationary night blindness
|
C536122 |
|
|
incomplete, autosomal recessive CSNB
|
C536122 |
|
|
X-linked congenital stationary night blindness
|
C536122 |
|
