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Diseases
Genes (359)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Thalassemia
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
NF1
Fibrous Dysplasia Of Bone
Neurofibromatosis
PTEN
Thrombophlebitis
Protein Losing Enteropathy
PPP1R15A
Thalassemia
ITM2B
Cerebral Amyloid Angiopathy
NDP
Vascular Tumor
Uterine Rupture
NF2
Neurofibromatosis
DICER1
Pinealoblastoma
PLVAP
Protein Losing Enteropathy