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Diseases
Genes (620)
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TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
BEST1
Vitelliform Macular Dystrophy
MED12
Fg Syndrome
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
FAM20A
Enamel-Renal Syndrome
ASS1
Hyperoxia
Citrullinemia Type I
IFIH1
Singleton Merten Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
PTEN
Thrombophlebitis
Adenoid Cystic Carcinoma
Protein Losing Enteropathy
CD55
Protein Losing Enteropathy
TP53
Adenoid Cystic Carcinoma
IGFBP2
Adenoid Cystic Carcinoma
Hyperoxia
CYP1A1
Hyperoxia
NOTCH1
Adenoid Cystic Carcinoma
PIK3CA
Adenoid Cystic Carcinoma
PRPH2
Vitelliform Macular Dystrophy
MYBL1
Adenoid Cystic Carcinoma
FBXW7
Adenoid Cystic Carcinoma
BCOR
Adenoid Cystic Carcinoma