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Diseases
Genes (833)
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CEP290
Meckel Syndrome, Type 11
Retinitis Pigmentosa 57
Joubert Syndrome 16
MYO5B
Microvillus Inclusion Disease
Fanconi Renotubular Syndrome 2
RPGRIP1
Meckel Syndrome, Type 11
Retinitis Pigmentosa 57
C8orf37
Retinitis Pigmentosa 57
TMEM231
Meckel Syndrome, Type 11
Joubert Syndrome 16
PDE6B
Retinitis Pigmentosa 57
PDE6A
Retinitis Pigmentosa 57
CRX
Pinealoblastoma
Retinitis Pigmentosa 57
RPGR
Retinitis Pigmentosa 57
RPE65
Retinitis Pigmentosa 57
VSX2
Retinitis Pigmentosa 57
Microphthalmia, Isolated 2
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
LPIN2
Majeed Syndrome
CC2D2A
Meckel Syndrome, Type 11
Retinitis Pigmentosa 57
Joubert Syndrome 16
PDE6G
Retinitis Pigmentosa 57
LRAT
Retinitis Pigmentosa 57
TAF2
Mental Retardation, Autosomal Recessive 40
MC2R
Familial Glucocorticoid Deficiency
KANK2
Palmoplantar Keratoderma And Woolly Hair
CEP19
Morbid Obesity And Spermatogenic Failure