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Diseases
Genes (811)
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GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ABHD5
Cerebral Creatine Deficiency
ND4
Deafness, Sensorineural, Autosomal-Mitochondrial Type
Leber Optic Atrophy, Susceptibility To
ND6
Leber Optic Atrophy, Susceptibility To
ABCD1
Adrenoleukodystrophy
GAMT
Guanidinoacetate Methyltransferase Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
KCNC3
Spinocerebellar Ataxia Type-13
HSF4
Cataract 5, Multiple Types
ND1
Leber Optic Atrophy, Susceptibility To
ND5
Leber Optic Atrophy, Susceptibility To
TTR
Cerebral Creatine Deficiency
Adrenoleukodystrophy
Familial Amyloid Neuropathy
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ND4L
Leber Optic Atrophy, Susceptibility To
ATP6
Leber Optic Atrophy, Susceptibility To
PAH
Phenylketonuria
Galactose-1-Phosphate Uridylyltransferase Deficiency
Bladder Exstrophy
CYTB
Leber Optic Atrophy, Susceptibility To
COX3
Leber Optic Atrophy, Susceptibility To
COX1
Deafness, Sensorineural, Autosomal-Mitochondrial Type
Leber Optic Atrophy, Susceptibility To