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Diseases
Genes (1986)
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KRT17
Pachyonychia Congenita
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
Autosomal Dominant Polycystic Kidney Disease
Pachyonychia Congenita 2
Hyperhidrosis
KRT16
Pachyonychia Congenita
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
Pachyonychia Congenita 2
Hyperhidrosis
KRT6A
Pachyonychia Congenita
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
Pachyonychia Congenita 2
Hyperhidrosis
KRT6B
Pachyonychia Congenita
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita
Pachyonychia Congenita 3
Autosomal Dominant Polycystic Kidney Disease
Pachyonychia Congenita 2
Hyperhidrosis
PC
Pyruvate Carboxylase Deficiency
Pyruvate Carboxylase Deficiency
Pyruvate Carboxylase Deficiency, Infantile Type
BUB1B
Premature Chromatid Separation Trait
Mosaic Variegated Aneuploidy Syndrome 1
KRT10
Pachyonychia Congenita
Pachyonychia Congenita 1
Pachyonychia Congenita 4
Pachyonychia Congenita 3
Pachyonychia Congenita 2
PKD2
Autosomal Dominant Polycystic Kidney Disease
PKD1
Autosomal Dominant Polycystic Kidney Disease
GNA11
Uveal Melanoma
BAP1
Uveal Melanoma
GNAQ
Uveal Melanoma
CEP57
Mosaic Variegated Aneuploidy Syndrome 1
SCN4A
Paramyotonia Congenita
TP53
Autosomal Dominant Polycystic Kidney Disease
Uveal Melanoma
Familial Pancreatic Carcinoma
Pediatric Ependymoma
Hyperhidrosis
Medulloblastoma
GANAB
Autosomal Dominant Polycystic Kidney Disease
SF3B1
Uveal Melanoma
HLA-B
Ankylosing Spondylitis
Hyperhidrosis
TRIP13
Mosaic Variegated Aneuploidy Syndrome 1
CDKN2A
Uveal Melanoma
Familial Pancreatic Carcinoma
Ankylosing Spondylitis
Pediatric Ependymoma
Medulloblastoma