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Diseases
Genes (198)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
DDX58
Singleton Merten Syndrome
KDM3B
Metal Toxicity
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
PTEN
Thrombophlebitis
Protein Losing Enteropathy
ITM2B
Cerebral Amyloid Angiopathy
NDP
Vascular Tumor
Uterine Rupture
KDR
Lathyrism
DICER1
Pinealoblastoma
PLVAP
Protein Losing Enteropathy
DGAT1
Protein Losing Enteropathy