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Diseases
Genes (633)
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WRN
Werner Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
NLRP3
Muckle–wells Syndrome
ND5
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
PQBP1
Renpenning's Syndrome
ND1
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
Machado–joseph Disease
FAM20A
Enamel-Renal Syndrome
ACTG2
Berdon Syndrome
ND6
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
ATXN3
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
Machado–joseph Disease
IFIH1
Singleton Merten Syndrome
TRNS1
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
TRNW
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
TRNF
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
TRNQ
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
COX1
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
APOA1
Childhood Obesity
Werner Syndrome
Familial Isolated Vitamin E Deficiency
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
ASS1
Citrullinemia Type I