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Diseases
Genes (540)
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ND6
Leber Optic Atrophy
AFG3L2
Spinocerebellar Ataxia Type 28
TTPA
Familial Isolated Vitamin E Deficiency
ND1
Leber Optic Atrophy
ND4
Leber Optic Atrophy
ND5
Leber Optic Atrophy
TFAP2A
Branchiooculofacial Syndrome
ND4L
Leber Optic Atrophy
ATP6
Leber Optic Atrophy
CYTB
Leber Optic Atrophy
PQBP1
Renpenning's Syndrome
COX3
Leber Optic Atrophy
ND2
Leber Optic Atrophy
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
IFIH1
Singleton Merten Syndrome
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3