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Diseases
Genes (1152)
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TTPA
Familial Isolated Vitamin E Deficiency
MED12
Mitral Valve Prolapse
Fg Syndrome
Ventricular Septal Defect
PQBP1
Renpenning's Syndrome
Ventricular Septal Defect
UBE3B
Kaufman Oculocerebrofacial Syndrome
Ventricular Septal Defect
TCN2
Transcobalamin Deficiency
NKX2-5
Myotonic Dystrophy
Ventricular Septal Defect
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
FLNA
Mitral Valve Prolapse 1
Mitral Valve Prolapse
Intestinal Neuronal Dysplasia
Fg Syndrome
IFIH1
Singleton Merten Syndrome
DCHS1
Mitral Valve Prolapse 1
Mitral Valve Prolapse
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
IRX4
Adenoid Cystic Carcinoma
Ventricular Septal Defect
BCOR
Mitral Valve Prolapse
Adenoid Cystic Carcinoma
Ventricular Septal Defect
HRAS
Mitral Valve Prolapse
Adenoid Cystic Carcinoma
Ventricular Septal Defect
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome