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Diseases
Genes (146)
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TTPA
Familial Isolated Vitamin E Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
SLC4A1
Southeast Asian Ovalocytosis
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
PRNP
Kuru, Susceptibility To
Akinetic Mutism
SRD5A2
5α-Reductase Deficiency
PAH
Phenylketonuria
RB1
Pinealoblastoma
Trilateral Retinoblastoma
DDX58
Singleton Merten Syndrome
SLC11A1
Buruli Ulcer
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
G6PD
Southeast Asian Ovalocytosis
Phenylketonuria
Renpenning's Syndrome
SMOC1
Klippel-Trenaunay-Weber Syndrome
CAT
Phenylketonuria
NEFH
Phenylketonuria
PSPH
Phenylketonuria