Mitochondrial Complex I Deficiency, Nuclear Type 18 (MC1DN18)

Alias:

Mc1dn18

Mitochondrial Complex 1 Deficiency, Nuclear Type 18

Nuclear Type Mitochondrial Complex I Deficiency 18

Mi Complex I Deficiency, Nuclear Type 18

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Mitochondrial Complex I Deficiency, Nuclear Type 18, is also known as mc1dn18. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 18 is NDUFAF3 (NADH:Ubiquinone Oxidoreductase Complex Assembly Factor 3). Affiliated tissues include liver and eye, and related phenotypes are decreased activity of mitochondrial complex i and optic disc pallor

Related ID：

MALACARDS：MTC165

OMIM：618240

MESH：D028361