Visualize Submit Comment
Metadata
ID DOID:0080118
Name mitochondrial complex III deficiency nuclear type 9
Definition A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC3 gene on chromosome 11q12.
http://omim.org/entry/616111?search=616111&highlight=616111
Xrefs

OMIM:616111

Parent Relationships

is_a mitochondrial complex III deficiency

Add an item to the term tracker