RS267606891 MT-ND3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Leber optic atrophy and dystonia
Mitochondrial complex I deficiency
mitochondrial type 1
Leigh syndrome
Mitochondrial DNA-Associated Leigh Syndrome and NARP
Mitochondrial disease
See cases
Mitochondrial myopathy
episodic
with optic atrophy and reversible leukoencephalopathy
Primary mitochondrial disorders
Leber optic atrophy and dystonia
Mitochondrial complex I deficiency
mitochondrial type 1
Leigh syndrome
Other Variants in MT-ND3