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Summary Literature (0)
MIM:124000 - MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1

Xenbase Genes: bcs1l, uqcrq

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007415 - mitochondrial complex III deficiency nuclear type 1
MONDO:0015448 - mitochondrial complex III deficiency
MONDO:0016811 - renal tubulopathy-encephalopathy-liver failure syndrome

Disease Ontology (DO):
DOID:0080111 - mitochondrial complex III deficiency nuclear type 1