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Diseases
Genes (241)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
KDM3B
Metal Toxicity
DDX58
Singleton Merten Syndrome
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
GNAS
Fibrous Dysplasia Of Bone