mitochondrial complex III deficiency, nuclear type 11

Rare Disease

MONDO:0859321

Definition

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCRH gene.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

mitochondrial complex III deficiency nuclear type 1

MONDO:0007415

mitochondrial complex III deficiency nuclear type 2

MONDO:0014063

mitochondrial complex III deficiency nuclear type 3

MONDO:0014064

mitochondrial complex III deficiency nuclear type 4

MONDO:0014065

mitochondrial complex III deficiency nuclear type 5

MONDO:0014066

mitochondrial complex III deficiency nuclear type 6

MONDO:0014194