Mitochondrial Complex I Deficiency, Nuclear Type 33 (MC1DN33)

Alias:

Mc1dn33

Mitochondrial Complex 1 Deficiency, Nuclear Type 33

Nuclear Type Mitochondrial Complex I Deficiency 33

Mi Complex I Deficiency, Nuclear Type 33

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Mitochondrial Complex I Deficiency, Nuclear Type 33, also known as mc1dn33, is related to chromosome 17q12 deletion syndrome and charcot-marie-tooth disease, type 4b3. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 33 is NDUFA6 (NADH:Ubiquinone Oxidoreductase Subunit A6). Affiliated tissues include liver, and related phenotypes are seizure and optic atrophy

Related ID：

MALACARDS：MTC178

OMIM：618253

MESH：D028361