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Diseases
Genes (1031)
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KRT17
Pachyonychia Congenita
Pachyonychia Congenita 2
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
Autosomal Dominant Polycystic Kidney Disease
KRT16
Pachyonychia Congenita
Pachyonychia Congenita 2
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
KRT6A
Pachyonychia Congenita
Pachyonychia Congenita 2
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
KRT6B
Pachyonychia Congenita
Pachyonychia Congenita 2
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
Autosomal Dominant Polycystic Kidney Disease
BUB1B
Mosaic Variegated Aneuploidy Syndrome 1
Premature Chromatid Separation Trait
KRT10
Pachyonychia Congenita
Pachyonychia Congenita 2
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita 3
PC
Pyruvate Carboxylase Deficiency
Pyruvate Carboxylase Deficiency
PKD2
Autosomal Dominant Polycystic Kidney Disease
SCN4A
Paramyotonia Congenita
PKD1
Autosomal Dominant Polycystic Kidney Disease
CEP57
Mosaic Variegated Aneuploidy Syndrome 1
ESCO2
Roberts Syndrome
GANAB
Autosomal Dominant Polycystic Kidney Disease
TRIP13
Mosaic Variegated Aneuploidy Syndrome 1
C4B
Complement Component 4b Deficiency
MAPT
Tauopathy
TP63
Primary Ovarian Insufficiency
Bladder Exstrophy
NFE2L2
Pachyonychia Congenita
Pachyonychia Congenita 2
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita 3
Autosomal Dominant Polycystic Kidney Disease
Tauopathy
Primary Ovarian Insufficiency
ISL1
Bladder Exstrophy
BMP15
Primary Ovarian Insufficiency