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Diseases
Genes (830)
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SLC12A6
Andermann Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
TNFAIP3
Haploinsufficiency Of A20
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
TP63
Squamous-Cell Carcinoma Of The Lung
Bladder Exstrophy
CFH
Membranoproliferative Glomerulonephritis
FGFR2
Squamous-Cell Carcinoma Of The Lung
ASS1
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
KRAS
Squamous-Cell Carcinoma Of The Lung
Bladder Exstrophy
EGFR
Squamous-Cell Carcinoma Of The Lung
Enamel-Renal Syndrome
DDR2
Squamous-Cell Carcinoma Of The Lung
ISL1
Bladder Exstrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
EPHA2
Squamous-Cell Carcinoma Of The Lung
FGFR1
Squamous-Cell Carcinoma Of The Lung
TGFBR2
Membranoproliferative Glomerulonephritis
Squamous-Cell Carcinoma Of The Lung
Uterine Rupture