Mitochondrial complex III deficiency nuclear type 1

MONDO:0007415

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the BCS1L gene.

Also known as: BCS1L mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in BCS1L, Complex 3 mitochondrial respiratory chain deficiency, MC3DN1, mitochondrial Complex 3 deficiency, nuclear type 1, mitochondrial complex III deficiency, mitochondrial complex III deficiency, nuclear type 1

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 1 itself.

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↑ Mitochondrial complex III deficiency, nuclear type (0)

Sub-types of Mitochondrial complex III deficiency nuclear type 1

Renal tubulopathy-encephalopathy-liver failure syndrome 0 trials

Including sub-types (13) Tagged with Mitochondrial complex III deficiency nuclear type 1 (0)

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