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Diseases
Genes (1398)
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COL2A1
Arthritis
Spondyloepiphyseal Dysplasia Congenita
TBX5
Arthritis
Holt–oram Syndrome
FGFR2
Jackson–weiss Syndrome
Night Blindness, Congenital Stationary, Autosomal Dominant 1
SMS
Snyder-Robinson Syndrome
MED12
Fg Syndrome
RHO
Night Blindness, Congenital Stationary, Autosomal Dominant 1
GRM6
Night Blindness, Congenital Stationary, Autosomal Dominant 1
TRPM1
Night Blindness, Congenital Stationary, Autosomal Dominant 1
TSC2
Lymphangioleiomyomatosis
RECQL4
Baller–gerold Syndrome
IGF2
Hemihypertrophy
Snyder-Robinson Syndrome
Lymphangioleiomyomatosis
LTBP4
Cutis Laxa, Autosomal Recessive, Type Ic
GNAT1
Night Blindness, Congenital Stationary, Autosomal Dominant 1
FGFR1
Arthritis
Jackson–weiss Syndrome
LRIT3
Night Blindness, Congenital Stationary, Autosomal Dominant 1
SLC24A1
Night Blindness, Congenital Stationary, Autosomal Dominant 1
PDE6B
Night Blindness, Congenital Stationary, Autosomal Dominant 1
GPR179
Night Blindness, Congenital Stationary, Autosomal Dominant 1
SAG
Night Blindness, Congenital Stationary, Autosomal Dominant 1
CACNA1F
Night Blindness, Congenital Stationary, Autosomal Dominant 1