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Diseases
Genes (1040)
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SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
RHO
Congenital Stationary Night Blindness
GRM6
Congenital Stationary Night Blindness
TRPM1
Congenital Stationary Night Blindness
RHBDF2
Howel–evans Syndrome
KRT17
Pachyonychia Congenita
TMEM67
Coach Syndrome
SS18
Synovial Sarcoma
RPGRIP1L
Coach Syndrome
CC2D2A
Coach Syndrome
GNAT1
Congenital Stationary Night Blindness
LRIT3
Congenital Stationary Night Blindness
SLC24A1
Congenital Stationary Night Blindness
PDE6B
Congenital Stationary Night Blindness
GPR179
Congenital Stationary Night Blindness
SAG
Congenital Stationary Night Blindness
CACNA1F
Congenital Stationary Night Blindness
NYX
Congenital Stationary Night Blindness